299 results on '"Graham L. Hall"'
Search Results
2. No association between in utero exposure to emissions from a coalmine fire and post-natal lung function
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Emily J. Hemstock, Rachel E. Foong, Graham L. Hall, Amanda J. Wheeler, Shyamali C. Dharmage, Marita Dalton, Grant J. Williamson, Caroline Gao, Michael J. Abramson, Fay H. Johnston, and Graeme R. Zosky
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Particulate matter ,Respiratory function ,Early life ,Long-term effects ,In utero exposure ,Diseases of the respiratory system ,RC705-779 - Abstract
Abstract Background and objective Studies linking early life exposure to air pollution and subsequent impaired lung health have focused on chronic, low-level exposures in urban settings. We aimed to determine whether in utero exposure to an acute, high-intensity air pollution episode impaired lung function 7-years later. Method We conducted a prospective cohort study of children who lived in the vicinity of a coalmine fire. Respiratory function was measured using the forced oscillation technique (FOT). Z-scores for resistance at 5 Hz (R5), reactance at 5 Hz (X5) and area under the reactance curve (AX) were calculated. Two sets of analyses were conducted to address two separate questions: (1) whether mine fire exposure (a binary indicator; conceived after the mine fire vs in utero exposed) was associated with the respiratory Z-scores; (2) whether there was any dose–response relationship between fire-related PM2.5 exposure and respiratory outcomes among those exposed. Results Acceptable lung function measurements were obtained from 79 children; 25 unexposed and 54 exposed in utero. Median (interquartile range) for daily average and peak PM2.5 for the exposed children were 4.2 (2.6 – 14.2) and 88 (52—225) µg/m3 respectively. There were no detectable differences in Z-scores between unexposed and exposed children. There were no associations between respiratory Z-scores and in utero exposure to PM2.5 (daily average or peak). Conclusion There was no detectable effect of in utero exposure to PM2.5 from a local coalmine fire on post-natal lung function 7-years later. However, statistical power was limited.
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- 2023
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3. The ventilatory response to hypoxia is blunted in some preterm infants during the second year of life
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Zoe Freislich, Benjamin Stoecklin, Naomi Hemy, J. Jane Pillow, Graham L. Hall, Andrew C. Wilson, and Shannon J. Simpson
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hypoxia ,infant ,premature ,bronchopulmonary dysplasia ,respiration ,artificial ,Pediatrics ,RJ1-570 - Abstract
BackgroundPreterm birth and subsequent neonatal ventilatory treatment disrupts development of the hypoxic ventilatory response (HVR). An attenuated HVR has been identified in preterm neonates, however it is unknown whether the attenuation persists into the second year of life. We investigated the HVR at 12–15 months corrected postnatal age and assessed predictors of a blunted HVR in those born very preterm (
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- 2022
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4. Characterisation of lung function trajectories and associated early-life predictors in an Australian birth cohort study
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Francesca Sanna, Francesca Locatelli, Peter D. Sly, Elisha White, David Blake, Jane Heyworth, Graham L. Hall, and Rachel E. Foong
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Medicine - Abstract
Background There is growing evidence that lung function in early-life predicts later lung function. Adverse events over the lifespan might influence an individual's lung function trajectory, resulting in poor respiratory health. The aim of this study is to identify early-life risk factors and their impact on lung function trajectories to prevent long-term lung impairments. Methods Our study included participants from the Raine Study, a prospective pregnancy cohort, with at least two spirometry measurements. Lung function trajectories from the 6- to 22-year follow-ups were characterised using finite mixture modelling. Multinomial logistic regression analyses were used to evaluate the association between early-life predictors and lung function trajectories. Main results A total of 1512 participants (768 males, 744 females), representing 53% of the whole cohort, were included in this analysis. Four lung function trajectories of forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC) and FEV1/FVC (z-scores) were identified. FEV1 and FVC trajectories were categorised as: “very low”, “low”, “average” and “above average”, respectively. Based on their shape, lung function trajectories of FEV1/FVC were categorised as “very low”, “low–average”, “average–low” and “average”. Asthma and maternal smoking were identified as risk factors for low lung function trajectories in this cohort, as well as early-life exposure to PM2.5Absorbance. Conclusions Early-life risk factors may influence lung function trajectories over time. Nonetheless, identifying children with a high risk of having low lung function trajectories should be prioritised to prevent deficits in later life.
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- 2022
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5. Clinical significance and applications of oscillometry
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David A. Kaminsky, Shannon J. Simpson, Kenneth I. Berger, Peter Calverley, Pedro L. de Melo, Ronald Dandurand, Raffaele L. Dellacà, Claude S. Farah, Ramon Farré, Graham L. Hall, Iulia Ioan, Charles G. Irvin, David W. Kaczka, Gregory G. King, Hajime Kurosawa, Enrico Lombardi, Geoffrey N. Maksym, François Marchal, Ellie Oostveen, Beno W. Oppenheimer, Paul D. Robinson, Maarten van den Berge, and Cindy Thamrin
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Diseases of the respiratory system ,RC705-779 - Abstract
Recently, “Technical standards for respiratory oscillometry” was published, which reviewed the physiological basis of oscillometric measures and detailed the technical factors related to equipment and test performance, quality assurance and reporting of results. Here we present a review of the clinical significance and applications of oscillometry. We briefly review the physiological principles of oscillometry and the basics of oscillometry interpretation, and then describe what is currently known about oscillometry in its role as a sensitive measure of airway resistance, bronchodilator responsiveness and bronchial challenge testing, and response to medical therapy, particularly in asthma and COPD. The technique may have unique advantages in situations where spirometry and other lung function tests are not suitable, such as in infants, neuromuscular disease, sleep apnoea and critical care. Other potential applications include detection of bronchiolitis obliterans, vocal cord dysfunction and the effects of environmental exposures. However, despite great promise as a useful clinical tool, we identify a number of areas in which more evidence of clinical utility is needed before oscillometry becomes routinely used for diagnosing or monitoring respiratory disease.
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- 2022
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6. A Preliminary Investigation of Mobile Respiratory Function Testing in Western Australian Communities
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Petra Czarniak, Kim Watkins, Finbarr Foy, Richard Parsons, Graham L. Hall, and Bruce Sunderland
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asthma ,chronic obstructive pulmonary disease ,COPD ,spirometry ,lung function testing ,Technology ,Engineering (General). Civil engineering (General) ,TA1-2040 ,Biology (General) ,QH301-705.5 ,Physics ,QC1-999 ,Chemistry ,QD1-999 - Abstract
Although underutilized, spirometry is essential in the diagnosis and management of chronic obstructive pulmonary disease (COPD) and asthma. This study aimed to investigate a mobile (i.e., transportable) lung function testing (LFT) services in two metropolitan and two rural clinics in Western Australia. Individuals attending a mobile LFT clinic in 2021 were invited to complete questionnaires at baseline and after 6–8 weeks. Questionnaires were completed by 59/74 (79.7%) respondents (mean age 62.5 ± 14.2 years); most were female (35/59; 59.3%). A history of asthma was reported in 50.9% (30/59) and COPD in 18.6% (11/59) of respondents [13.6% (8/59) reported both]. At baseline, most (22/30; 73.3%) had asthma control test scores ≤19 (mean 16.6; range 8.0–25.0); at follow-up, 16/31 (51.6%) had scores ≤19 (mean score 18.0; range 6.0–25.0). Of the 11 diagnosed with COPD at baseline, the mean Clinical COPD Questionnaire and COPD assessment test scores were greater at follow-up (1.9 vs. 2.3; and: 10.3 vs. 14.7 respectively), reflecting worsening disease. Most participants (57/59; 96.6%) were satisfied with the LFT experience. The role of mobile LFT services to optimize the diagnosis and management of chronic lung disease and to minimize patient burden requires further investigation to improve short term patient outcomes.
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- 2023
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7. Variants associated with HHIP expression have sex-differential effects on lung function [version 2; peer review: 2 approved]
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Katherine A. Fawcett, Ma'en Obeidat, Carl Melbourne, Nick Shrine, Anna L. Guyatt, Catherine John, Jian'an Luan, Anne Richmond, Marta R. Moksnes, Raquel Granell, Stefan Weiss, Medea Imboden, Sebastian May-Wilson, Pirro Hysi, Thibaud S. Boutin, Laura Portas, Claudia Flexeder, Sarah E. Harris, Carol A. Wang, Leo-Pekka Lyytikäinen, Teemu Palviainen, Rachel E. Foong, Dirk Keidel, Cosetta Minelli, Claudia Langenberg, Yohan Bossé, Maarten Van den Berge, Don D. Sin, Ke Hao, Archie Campbell, David Porteous, Sandosh Padmanabhan, Blair H. Smith, David M. Evans, Sue Ring, Arnulf Langhammer, Kristian Hveem, Cristen Willer, Ralf Ewert, Beate Stubbe, Nicola Pirastu, Lucija Klaric, Peter K. Joshi, Karina Patasova, Mangino Massimo, Ozren Polasek, John M. Starr, Stefan Karrasch, Konstantin Strauch, Thomas Meitinger, Igor Rudan, Taina Rantanen, Kirsi Pietiläinen, Mika Kähönen, Olli T. Raitakari, Graham L. Hall, Peter D. Sly, Craig E. Pennell, Jaakko Kaprio, Terho Lehtimäki, Veronique Vitart, Ian J. Deary, Debbie Jarvis, James F. Wilson, Tim Spector, Nicole Probst-Hensch, Nicholas J. Wareham, Henry Völzke, John Henderson, David P. Strachan, Ben M. Brumpton, Caroline Hayward, Ian P. Hall, Martin D. Tobin, and Louise V. Wain
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Medicine ,Science - Abstract
Background: Lung function is highly heritable and differs between the sexes throughout life. However, little is known about sex-differential genetic effects on lung function. We aimed to conduct the first genome-wide genotype-by-sex interaction study on lung function to identify genetic effects that differ between males and females. Methods: We tested for interactions between 7,745,864 variants and sex on spirometry-based measures of lung function in UK Biobank (N=303,612), and sought replication in 75,696 independent individuals from the SpiroMeta consortium. Results: Five independent single-nucleotide polymorphisms (SNPs) showed genome-wide significant (P
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- 2021
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8. Variants associated with HHIP expression have sex-differential effects on lung function [version 1; peer review: 2 approved]
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Katherine A. Fawcett, Ma'en Obeidat, Carl Melbourne, Nick Shrine, Anna L. Guyatt, Catherine John, Jian'an Luan, Anne Richmond, Marta R. Moksnes, Raquel Granell, Stefan Weiss, Medea Imboden, Sebastian May-Wilson, Pirro Hysi, Thibaud S. Boutin, Laura Portas, Claudia Flexeder, Sarah E. Harris, Carol A. Wang, Leo-Pekka Lyytikäinen, Teemu Palviainen, Rachel E. Foong, Dirk Keidel, Cosetta Minelli, Claudia Langenberg, Yohan Bossé, Maarten Van den Berge, Don D. Sin, Ke Hao, Archie Campbell, David Porteous, Sandosh Padmanabhan, Blair H. Smith, David M. Evans, Sue Ring, Arnulf Langhammer, Kristian Hveem, Cristen Willer, Ralf Ewert, Beate Stubbe, Nicola Pirastu, Lucija Klaric, Peter K. Joshi, Karina Patasova, Mangino Massimo, Ozren Polasek, John M. Starr, Stefan Karrasch, Konstantin Strauch, Thomas Meitinger, Igor Rudan, Taina Rantanen, Kirsi Pietiläinen, Mika Kähönen, Olli T. Raitakari, Graham L. Hall, Peter D. Sly, Craig E. Pennell, Jaakko Kaprio, Terho Lehtimäki, Veronique Vitart, Ian J. Deary, Debbie Jarvis, James F. Wilson, Tim Spector, Nicole Probst-Hensch, Nicholas J. Wareham, Henry Völzke, John Henderson, David P. Strachan, Ben M. Brumpton, Caroline Hayward, Ian P. Hall, Martin D. Tobin, and Louise V. Wain
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Medicine ,Science - Abstract
Background: Lung function is highly heritable and differs between the sexes throughout life. However, little is known about sex-differential genetic effects on lung function. We aimed to conduct the first genome-wide genotype-by-sex interaction study on lung function to identify genetic effects that differ between males and females. Methods: We tested for interactions between 7,745,864 variants and sex on spirometry-based measures of lung function in UK Biobank (N=303,612), and sought replication in 75,696 independent individuals from the SpiroMeta consortium. Results: Five independent single-nucleotide polymorphisms (SNPs) showed genome-wide significant (P
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- 2020
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9. Persistent activation of interlinked type 2 airway epithelial gene networks in sputum-derived cells from aeroallergen-sensitized symptomatic asthmatics
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Anya C. Jones, Niamh M. Troy, Elisha White, Elysia M. Hollams, Alexander M. Gout, Kak-Ming Ling, Anthony Kicic, Stephen M. Stick, Peter D. Sly, Patrick G. Holt, Graham L. Hall, and Anthony Bosco
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Medicine ,Science - Abstract
Abstract Atopic asthma is a persistent disease characterized by intermittent wheeze and progressive loss of lung function. The disease is thought to be driven primarily by chronic aeroallergen-induced type 2-associated inflammation. However, the vast majority of atopics do not develop asthma despite ongoing aeroallergen exposure, suggesting additional mechanisms operate in conjunction with type 2 immunity to drive asthma pathogenesis. We employed RNA-Seq profiling of sputum-derived cells to identify gene networks operative at baseline in house dust mite-sensitized (HDMS) subjects with/without wheezing history that are characteristic of the ongoing asthmatic state. The expression of type 2 effectors (IL-5, IL-13) was equivalent in both cohorts of subjects. However, in HDMS-wheezers they were associated with upregulation of two coexpression modules comprising multiple type 2- and epithelial-associated genes. The first module was interlinked by the hubs EGFR, ERBB2, CDH1 and IL-13. The second module was associated with CDHR3 and mucociliary clearance genes. Our findings provide new insight into the molecular mechanisms operative at baseline in the airway mucosa in atopic asthmatics undergoing natural aeroallergen exposure, and suggest that susceptibility to asthma amongst these subjects involves complex interactions between type 2- and epithelial-associated gene networks, which are not operative in equivalently sensitized/exposed atopic non-asthmatics.
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- 2018
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10. Increased prevalence of expiratory flow limitation during exercise in children with bronchopulmonary dysplasia
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Christopher A. O'Dea, Karla Logie, Andrew Maiorana, Andrew C. Wilson, J. Jane Pillow, Georgia L Banton, Shannon J. Simpson, and Graham L. Hall
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Medicine - Abstract
Evidence regarding the prevalence of expiratory flow limitation (EFL) during exercise and the ventilatory response to exercise in children born preterm is limited. This study aimed to determine the prevalence of EFL as well as contributing factors to EFL and the ventilatory response to exercise in preterm children with and without bronchopulmonary dysplasia (BPD). Preterm children (≤32 weeks gestational age) aged 9–12 years with (n=64) and without (n=42) BPD and term controls (n=43), performed an incremental treadmill exercise test with exercise tidal flow–volume loops. More preterm children with BPD (53%) had EFL compared with preterm children without BPD (26%) or term controls (28%) (p
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- 2018
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11. The clinical utility of lung clearance index in early cystic fibrosis lung disease is not impacted by the number of multiple-breath washout trials
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Rachel E. Foong, Alana J. Harper, Billy Skoric, Louise King, Lidija Turkovic, Miriam Davis, Charles C. Clem, Tim Rosenow, Stephanie D. Davis, Sarath Ranganathan, Graham L. Hall, and Kathryn A. Ramsey
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Medicine - Abstract
The lung clearance index (LCI) from the multiple-breath washout (MBW) test is a promising surveillance tool for pre-school children with cystic fibrosis (CF). Current guidelines for MBW testing recommend that three acceptable trials are required. However, success rates to achieve these criteria are low in children aged
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- 2018
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12. The impact of respiratory viruses on lung health after preterm birth
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Nada Townsi, Ingrid A. Laing, Graham L. Hall, and Shannon J. Simpson
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Viruses ,respiratory infection ,preterm ,lung ,infants ,bronchopulmonary dysplasia ,Diseases of the respiratory system ,RC705-779 - Abstract
Children born preterm, less than 37 weeks’ gestation, are at increased risk of viral respiratory infections and associated complications both during their initial birth hospitalisation and in their first years following discharge. This increased burden of viral respiratory infections is likely to have long term implications for lung health and function in individuals born preterm, particularly those with bronchopulmonary dysplasia. Several hypotheses have been put forward to explain the association between early life viral respiratory infection and development of suboptimal lung health and function later in life following preterm birth. Although preterm infants with diminished lung function, particularly small airways, might be particularly susceptible to asthma and wheezing disorders following viral infection, there is evidence that respiratory viruses can activate number of inflammatory and airway re-modelling pathways. Therefore, the aim of this review is to highlight the perinatal and early life risk factors that may contribute to increased susceptibility to viral respiratory infections among preterm infants during early life and to understand how respiratory viral infection may influence the development of abnormal lung health and function later in life.
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- 2018
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13. Asthma and allergies in a cohort of adolescents conceived with ART
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Laura A. Wijs, Dorota A. Doherty, Jeffrey A. Keelan, Blagica Penova-Veselinovic, Peter Burton, John L. Yovich, Graham L. Hall, Peter D. Sly, Patrick G. Holt, and Roger J. Hart
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Adult ,Cohort Studies ,Adolescent ,Reproductive Techniques, Assisted ,Reproductive Medicine ,Humans ,Obstetrics and Gynecology ,Prospective Studies ,Asthma ,Food Hypersensitivity ,Developmental Biology - Abstract
Are asthma and allergies more common in adolescents conceived with assisted reproductive technologies (ART) compared with adolescents conceived without?The Growing Up Healthy Study (GUHS) is a prospective cohort study including ART-conceived offspring born between 1991 and 2001 in Perth, Australia. Their long-term health outcomes, including asthma and allergy parameters, were compared with those of their counterparts conceived without ART from the Raine Study Generation 2 (Gen2), born in 1989-1991. At age 14, 152 GUHS and 1845 Gen2 participants completed the following assessments: the International Studies of Asthma and Allergies in Childhood (ISAAC) questionnaire, spirometry, methacholine challenge testing and skin prick testing (SPT).No differences were detected in the prevalence of current asthma (7.7% versus 10.8%, adjusted odds ratio [aOR] 0.82 (95% CI 0.44-1.52), P = 0.530). Spirometry-measured lung volumes were larger in the ART adolescents. Bronchial hyperresponsiveness was less prevalent in the ART cohort (8.8 versus 18.6%, P = 0.006). Current allergic rhinoconjunctivitis (ARC) rates were significantly higher in the ART cohort (32.4% versus 25.2%, aOR 1.52 [95% CI 1.03-2.26], P = 0.036), with no cohort differences in atopic dermatitis. Food allergies were more prevalent in the ART cohort (20.7 versus 10.9%, aOR 1.89 [95% CI 1.17-3.06], P = 0.010) with more adolescents having a positive SPT (68.0% versus 45.4%, aOR 3.03 [95% 1.99-4.63], P0.001).This study reports no differences in asthma prevalence, slightly altered lung function, an increase in ARC, food allergies and positive SPT in the ART-conceived adolescents. These findings are important to families and healthcare providers and may open up possibilities for targeted screening and treatment. Further studies are required to confirm these findings.
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- 2022
14. Association between early respiratory viral infections and structural lung disease in infants with cystic fibrosis
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Don B. Sanders, Ashley R. Deschamp, Joseph E. Hatch, James E. Slaven, Netsanet Gebregziabher, Mariette Kemner-van de Corput, Harm A.W.M. Tiddens, Tim Rosenow, Gregory A. Storch, Graham L. Hall, Stephen M. Stick, Sarath Ranganathan, Thomas W. Ferkol, Stephanie D. Davis, Radiology & Nuclear Medicine, and Pediatrics
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Pulmonary and Respiratory Medicine ,Cystic Fibrosis ,Cough ,SDG 3 - Good Health and Well-being ,Virus Diseases ,Pediatrics, Perinatology and Child Health ,Viruses ,Infant ,Humans ,Lung ,Respiratory Tract Infections - Abstract
Background: Infants with cystic fibrosis (CF) develop structural lung disease early in life, and viral infections are associated with progressive lung disease. We hypothesized that the presence of respiratory viruses would be associated with structural lung disease on computed tomography (CT) of the chest in infants with CF. Methods: Infants with CF were enrolled before 4 months of age. Multiplex PCR assays were performed on nasal swabs to detect respiratory viruses during routine visits and when symptomatic. Participants underwent CT imaging at approximately 12 months of age. Associations between Perth–Rotterdam Annotated Grid Morphometric Analysis for CF (PRAGMA-CF) CT scores and respiratory viruses and symptoms were assessed with Spearman correlation coefficients. Results: Sixty infants were included for analysis. Human rhinovirus was the most common virus detected, on 28% of tested nasal swabs and in 85% of participants. The median (IQR) extent of lung fields that was healthy based on PRAGMA-CF was 98.7 (0.8)%. There were no associations between PRAGMA-CF and age at first virus, or detection of any virus, including rhinovirus, respiratory syncytial virus, or parainfluenza. The extent of airway wall thickening was associated with ever having wheezed (ρ = 0.31, p = 0.02) and number of encounters with cough (ρ = 0.25, p = 0.0495). Conclusions: Infants with CF had minimal structural lung disease. We did not find an association between respiratory viruses and CT abnormalities. Wheezing and frequency of cough were associated with early structural changes.
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- 2022
15. Factors influencing participation in home, school, and community settings by children and adolescents with neuromuscular disorders: A qualitative descriptive study
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Aysha Stroobach, Andrew C. Wilson, Jenny Lam, Graham L. Hall, Adelaide Withers, and Jenny Downs
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Developmental Neuroscience ,Pediatrics, Perinatology and Child Health ,Neurology (clinical) - Abstract
This study explored how children and adolescents with a neuromuscular disorder (NMD) and their parents experienced barriers and enablers to the child's participation.This was a qualitative descriptive design. Fourteen semi-structured interviews were conducted (n = 13 mothers, n = 4 fathers, n = 8 children and adolescents) including one to three family members for each interview according to their preference. Data were analysed by content analysis, using the family of Participation-Related Constructs (fPRC), to characterize the components of participation.Meaningful participation was illustrated in the personal categories of the fPRC including the child's sense of self, preferences, and competence to perform activities. Enablers and barriers related to adaptive equipment and activity modification, social relationships, inclusion, accessibility to venues, social attitudes, and policies.Personal motivators are critical to understanding what participation is meaningful to children and adolescents with NMDs. Social and physical supports within the child's immediate environment as well as accessibility and advocacy more widely in the community enable participation. The fPRC is a useful tool for understanding participation in these children; it informs how to support participation and suggests domains for evaluation in future intervention studies. Advocacy for participation should consider targets in the immediate and broader environments.
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- 2022
16. Quality of life is poorly correlated to lung disease severity in school-aged children with cystic fibrosis
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Danielle Wurzel, Suzanna Vidmar, Phillip Pattie, Arest Cf, Rachel E. Foong, Graham L. Hall, Sarath Ranganathan, Kathryn A. Ramsey, Joanne Harrison, and Alana Harper
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Pulmonary and Respiratory Medicine ,Spirometry ,medicine.medical_specialty ,Cystic Fibrosis ,medicine.diagnostic_test ,business.industry ,Health Status ,Australia ,medicine.disease ,Severity of Illness Index ,Cystic fibrosis ,Clinical trial ,Correlation ,Lung structure ,Quality of life ,Lung disease ,Internal medicine ,Pediatrics, Perinatology and Child Health ,Quality of Life ,medicine ,Humans ,Child ,business ,Lung ,Lung function - Abstract
Background There is no data exclusively on the relationship between health-related quality-of-life (HRQOL) and lung disease severity in early school-aged children with cystic fibrosis (CF). Using data from the Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST CF) we assessed the relationships between HRQOL, lung function and structure. Methods 125 children aged 6.5-10 years enrolled in the AREST CF program were included from CF clinics at Royal Children's Hospital (RCH), Melbourne (n = 66) and Perth Children's Hospital (PCH), Perth (n = 59), Australia. Demographics, HRQOL measured by Cystic Fibrosis Questionnaire-Revised (CFQ-R), spirometry, multiple-breath washout (MBW) and chest CT were collected across two years. Correlation between CFQ-R scores and lung structure/function parameters and agreement between parent-proxy and child-reported HRQOL were evaluated. Results No correlation was observed between most CFQ-R domain scores and FEV1 z-scores, excepting weak-positive correlation with parent CFQ-R Physical (rho = 0.21, CI 0.02-0.37), and Weight (rho = 0.21, CI 0.03-0.38) domain and child Body domain (rho = 0.26, CI 0.00-0.48). No correlation between most CFQ-R domain scores and LCI values was noted excepting weak-negative correlation with parent Respiratory (rho = -0.23, CI -0.41--0.05), Emotional (rho = -0.24, CI -0.43--0.04), and Physical (-0.21, CI -0.39--0.02) domains. Furthermore, structural lung disease on CT data demonstrated little to no association with CFQ-R parent and child domain scores. Additionally, no agreement between child self-report and parent-proxy CFQ-R scores was observed across the majority of domains and visits. Conclusion HRQOL correlated poorly with lung function and structure in early school-aged children with CF, hence clinical trials should consider these outcomes independently when determining study end-points.
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- 2022
17. Ivacaftor and Airway Inflammation in Preschool Children with Cystic Fibrosis
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Sarath Ranganathan, Barry Linnane, André Schultz, Graham L. Hall, Paul McNally, Yuliya V. Karpievitch, S. Stick, and Daryl Butler
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Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,biology ,business.industry ,Airway inflammation ,Inflammation ,Airway obstruction ,Critical Care and Intensive Care Medicine ,medicine.disease ,Cystic fibrosis ,Gastroenterology ,Broncho-alveolar lavage ,Cystic fibrosis transmembrane conductance regulator ,Ivacaftor ,Internal medicine ,medicine ,biology.protein ,Respiratory system ,medicine.symptom ,business ,medicine.drug - Published
- 2021
18. Development of a Symptom-Based Tool for Screening of Children at High Risk of Preschool Asthma
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Myrtha E. Reyna, Ruixue Dai, Maxwell M. Tran, Vanessa Breton, Maria Medeleanu, Wendy Y. W. Lou, Rachel E. Foong, Melanie Emmerson, Christoffer Dharma, Kozeta Miliku, Diana L. Lefebvre, Elinor Simons, Meghan B. Azad, Moira Chan-Yeung, Allan B. Becker, Piush J. Mandhane, Stuart E. Turvey, Graham L. Hall, Theo J. Moraes, Malcolm R. Sears, and Padmaja Subbarao
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Male ,Canada ,Cough ,Area Under Curve ,Child, Preschool ,Humans ,Female ,General Medicine ,Child ,Asthma ,Respiratory Sounds - Abstract
ImportanceDespite advances in asthma therapeutics, the burden remains highest in preschool children; therefore, it is critical to identify primary care tools that distinguish preschool children at high risk for burdensome disease for further evaluation. Current asthma prediction tools, such as the modified Asthma Predictive Index (mAPI), require invasive tests, limiting their applicability in primary care and low-resource settings.ObjectiveTo develop and evaluate the use of a symptom-based screening tool to detect children at high risk of asthma, persistent wheeze symptoms, and health care burden.Design, Setting, and ParticipantsThe cohort for this diagnostic study included participants from the CHILD Study (n = 2511) from January 1, 2008, to December 31, 2012, the Raine Study from January 1, 1989, to December 31, 2012 (n = 2185), and the Canadian Asthma Primary Prevention Study (CAPPS) from January 1, 1989, to December 31, 1995 (n = 349), with active follow-up to date. Data analysis was performed from November 1, 2019, to May 31, 2022.ExposuresThe CHILDhood Asthma Risk Tool (CHART) identified factors associated with asthma in patients at 3 years of age (timing and number of wheeze or cough episodes, use of asthma medications, and emergency department visits or hospitalizations for asthma or wheeze) to identify children with asthma or persistent symptoms at 5 years of age.Main Outcomes and MeasuresWithin the CHILD Study cohort, CHART was evaluated against specialist clinician diagnosis and the mAPI. External validation was performed in both a general population cohort (Raine Study [Australia]) and a high-risk cohort (CAPPS [Canada]). Predictive accuracy was measured by sensitivity, specificity, area under the receiver operating characteristic curve (AUROC), and positive and negative predicted values.ResultsAmong 2511 children (mean [SD] age at 3-year clinic visit, 3.08 [0.17] years; 1324 [52.7%] male; 1608 of 2476 [64.9%] White) with sufficient questionnaire data to apply CHART at 3 years of age, 2354 (93.7%) had available outcome data at 5 years of age. CHART applied in the CHILD Study at 3 years of age outperformed physician assessments and the mAPI in predicting persistent wheeze (AUROC, 0.94; 95% CI, 0.90-0.97), asthma diagnosis (AUROC, 0.73; 95% CI, 0.69-0.77), and health care use (emergency department visits or hospitalization for wheeze or asthma) (AUROC, 0.70; 95% CI, 0.61-0.78). CHART had a similar predictive performance for persistent wheeze in the Raine Study (N = 2185) in children at 5 years of age (AUROC, 0.82; 95% CI, 0.79-0.86) and CAPPS (N = 349) at 7 years of age (AUROC, 0.87; 95% CI, 0.80-0.94).Conclusions and RelevanceIn this diagnostic study, CHART was able to identify children at high risk of asthma at as early as 3 years of age. CHART could be easily incorporated as a routine screening tool in primary care to identify children who need monitoring, timely symptom control, and introduction of preventive therapies.
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- 2022
19. Bullying and psychosocial adjustment among children with and without asthma
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Mark L. Everard, Graham L. Hall, Kevin C. Runions, Rena Vithiatharan, and Donna Cross
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Social Psychology ,education ,05 social sciences ,Health condition ,Victimisation ,medicine.disease ,Mental health ,Education ,Victim status ,03 medical and health sciences ,0302 clinical medicine ,030225 pediatrics ,Developmental and Educational Psychology ,medicine ,0501 psychology and cognitive sciences ,Psychology ,Psychosocial ,050104 developmental & child psychology ,Asthma ,Clinical psychology - Abstract
Children with asthma face serious mental health risk, but the pathways remain unclear. This study aimed to examine bullying victimisation and perpetration in children with asthma and a comparison sample without a chronic health condition, and the role of bullying in moderating psychosocial adjustment outcomes for those with asthma. A sample of children with (n = 24) and without asthma (n = 39), and their parents, were recruited from hospital clinics. Parents rated children’s psychosocial adjustment; children provided self-report of bullying victimisation and perpetration; from which co-occurring bully/victim status was derived. No differences in mean perpetration or victimisation were found, but children with asthma were more likely to be bully/victims (involved both as target and perpetrator), compared to those without asthma. Children with asthma who were victims of bullying had greater peer problems and overall adjustment problems; bully/victims did not show this pattern. Children with asthma may be more likely to be bully/victims, and those who are victims of bullying may be at elevated risk for psychosocial adjustment problems and require particular support in this area from school counsellors and psychologists.
- Published
- 2021
20. Risk factors for poorer respiratory outcomes in adolescents and young adults born preterm
- Author
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Elizabeth F Smith, Naomi R Hemy, Graham L Hall, Andrew C Wilson, Conor P Murray, and Shannon J Simpson
- Subjects
Pulmonary and Respiratory Medicine - Abstract
RationaleThe respiratory outcomes for adult survivors of preterm birth in the postsurfactant era are wide-ranging with prognostic factors, especially those encountered after the neonatal period, poorly understood.ObjectivesTo obtain comprehensive ‘peak’ lung health data from survivors of very preterm birth and identify neonatal and life-course risk factors for poorer respiratory outcomes in adulthood.Methods127 participants born ≤32 weeks gestation (64%, n=81 with bronchopulmonary dysplasia (BPD), initially recruited according to a 2 with-BPD:1 without-BPD strategy), and 41 term-born controls completed a lung health assessment at 16–23 years, including lung function, imaging and symptom review. Risk factors assessed against poor lung health included neonatal treatments, respiratory hospitalisation in childhood, atopy and tobacco smoke exposure.Measurements and main resultsYoung adults born prematurely had greater airflow obstruction, gas trapping and ventilation inhomogeneity, in addition to abnormalities in gas transfer and respiratory mechanics, compared with term. Beyond lung function, we observed greater structural abnormalities, respiratory symptoms and inhaled medication use. A previous respiratory admission was associated with airway obstruction; mean forced expiratory volume in 1 s/forced vital capacity z-score was −0.561 lower after neonatal confounders were accounted for (95% CI −0.998 to –0.125; p=0.012). Similarly, respiratory symptom burden was increased in the preterm group with a respiratory admission, as was peribronchial thickening (6% vs 23%, p=0.010) and bronchodilator responsiveness (17% vs 35%, p=0.025). Atopy, maternal asthma and tobacco smoke exposure did not influence lung function or structure at 16–23 years in our preterm cohort.ConclusionsEven after accounting for the neonatal course, a respiratory admission during childhood remained significantly associated with reduced peak lung function in the preterm-born cohort, with the largest difference seen in those with BPD. A respiratory admission during childhood should, therefore, be considered a risk factor for long-term respiratory morbidity in those born preterm, especially for individuals with BPD.
- Published
- 2023
21. Pulmonary Gas Exchange Improves over the First Year in Preterm Infants with and without Bronchopulmonary Dysplasia
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Graham L. Hall, Benjamin Stoecklin, Y. Jane Choi, Dorota A. Doherty, J. Jane Pillow, Shannon J. Simpson, and Naomi Hemy
- Subjects
medicine.medical_specialty ,Pulmonary Gas Exchange ,business.industry ,Infant, Newborn ,Postmenstrual Age ,Infant ,First year of life ,Infant, Premature, Diseases ,medicine.disease ,Peripheral ,Postnatal age ,Bronchopulmonary dysplasia ,Lung disease ,Infant, Extremely Premature ,Internal medicine ,Pediatrics, Perinatology and Child Health ,medicine ,Cardiology ,Humans ,Infant, Very Low Birth Weight ,business ,Right shift ,Shunt (electrical) ,Bronchopulmonary Dysplasia ,Developmental Biology - Abstract
Background: Right shift of the peripheral oxyhaemoglobin saturation (SpO2) versus inspired oxygen pressure (PIO2) curve is a sensitive marker of pulmonary gas exchange. Objectives: The aim of this study was to assess the impact of prematurity and bronchopulmonary dysplasia (BPD) on gas exchange and right-to-left shunt in the neonatal period, and its evolution over the first year of life. Method: We assessed shift and shunt in extremely preterm (EP) and very preterm (VP) infants at 36 and 44 weeks’ postmenstrual age (PMA), and at 1-year corrected postnatal age (cPNA). PIO2 was decreased stepwise to achieve SpO2 between 85 and 98%. Shift and shunt were calculated from paired SpO2/PIO2 measurements using customized software. Results were examined cross-sectionally at each time point, and longitudinally using generalized linear regression. Term infants were assessed at 44 wk PMA as a comparative reference. Results: Longitudinal modelling showed continuous decline in shift in EP and VP infants during the first year of life. There was no difference in shift compared to term infants at 44 wk PMA (p = 0.094). EP infants with BPD had higher shift than infants without BPD at 36 wk PMA (p < 0.001) and 44 wk PMA (p = 0.005) but not at 1-year cPNA. Conclusions: In the absence of lung disease, prematurity per se did not result in reduced gas exchange at 1-year cPNA. We report ongoing, significant improvements in pulmonary gas exchange in all preterm infants during the first year of life, despite evidence of early deficits in gas exchange in EP infants with BPD.
- Published
- 2021
22. Choosing the Better Global Lung Initiative 2012 Equation in South African Population Groups
- Author
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Sanja Stanojevic, Reratilwe Ephenia Mphahlele, Rae Macginty, Sara-Jane Smith, Diane Gray, Refiloe Masekela, and Graham L. Hall
- Subjects
Pulmonary and Respiratory Medicine ,African population ,business.industry ,Correspondence ,MEDLINE ,Medicine ,Critical Care and Intensive Care Medicine ,business ,Demography - Published
- 2020
23. Multi-ancestry genome-wide association study improves resolution of genes, pathways and pleiotropy for lung function and chronic obstructive pulmonary disease
- Author
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Nick Shrine, Abril G Izquierdo, Jing Chen, Richard Packer, Robert J Hall, Anna L Guyatt, Chiara Batini, Rebecca J Thompson, Chandan Pavuluri, Vidhi Malik, Brian D Hobbs, Matthew Moll, Wonji Kim, Ruth Tal-Singer, Per Bakke, Katherine A Fawcett, Catherine John, Kayesha Coley, Noemi Nicole Piga, Alfred Pozarickij, Kuang Lin, Iona Y Millwood, Zhengming Chen, Liming Li, Sara RA Wielscher, Lies Lahousse, Guy Brusselle, Andre G Uitterlinden, Ani Manichaikul, Elizabeth C Oelsner, Stephen S Rich, R. Graham Barr, Shona M Kerr, Veronique Vitart, Michael R Brown, Matthias Wielscher, Medea Imboden, Ayoung Jeong, Traci M Bartz, Sina A Gharib, Claudia Flexeder, Stefan Karrasch, Christian Gieger, Annette Peters, Beate Stubbe, Xiaowei Hu, Victor E Ortega, Deborah A Meyers, Eugene R Bleecker, Stacey B Gabriel, Namrata Gupta, Albert Vernon Smith, Jian’an Luan, Jing-Hua Zhao, Ailin F Hansen, Arnulf Langhammer, Cristen Willer, Laxmi Bhatta, David Porteous, Blair H Smith, Archie Campbell, Tamar Sofer, Jiwon Lee, Martha L Daviglus, Bing Yu, Elise Lim, Hanfei Xu, George T O’Connor, Gaurav Thareja, Omar M E., Hamdi Mbarek, Karsten Suhre, Raquel Granell, Tariq O Faquih, Pieter S Hiemstra, Annelies M Slats, Benjamin H Mullin, Jennie Hui, Alan James, John Beilby, Karina Patasova, Pirro Hysi, Jukka T Koskela, Annah B Wyss, Jianping Jin, Sinjini Sikdar, Mikyeong Lee, Sebastian May-Wilson, Nicola Pirastu, Katherine A Kentistou, Peter K Joshi, Paul RHJ Timmers, Alexander T Williams, Robert C Free, Xueyang Wang, John L Morrison, Frank D Gilliland, Zhanghua Chen, Carol A Wang, Rachel E Foong, Sarah E Harris, Adele Taylor, Paul Redmond, James P Cook, Anubha Mahajan, Lars Lind, Teemu Palviainen, Terho Lehtimäki, Olli T Raitakari, Jaakko Kaprio, Taina Rantanen, Kirsi H Pietiläinen, Simon R Cox, Craig E Pennell, Graham L Hall, W. James Gauderman, Chris Brightling, James F Wilson, Tuula Vasankari, Tarja Laitinen, Veikko Salomaa, Dennis O Mook-Kanamori, Nicholas J Timpson, Eleftheria Zeggini, Josée Dupuis, Caroline Hayward, Ben Brumpton, Claudia Langenberg, Stefan Weiss, Georg Homuth, Carsten Oliver Schmidt, Nicole Probst-Hensch, Marjo-Riitta Jarvelin, Alanna C Morrison, Ozren Polasek, Igor Rudan, Joo-Hyeon Lee, Ian Sayers, Emma L Rawlins, Frank Dudbridge, Edwin K Silverman, David P Strachan, Robin G Walters, Andrew P Morris, Stephanie J London, Michael H Cho, Louise V Wain, Ian P Hall, and Martin D Tobin
- Abstract
Lung function impairment underlies chronic obstructive pulmonary disease (COPD) and predicts mortality. In the largest multi-ancestry GWAS meta-analysis of lung function to date, comprising 580,869 participants, 1020 independent association signals identified 559 genes supported by ≥2 criteria from a systematic variant-to-gene mapping framework. These genes were enriched in 29 pathways. Individual variants showed heterogeneity across ancestries, age and smoking groups, and collectively as a genetic risk score (GRS) showed strong association with COPD across ancestry groups. We undertook phenome-wide association studies (PheWAS) for selected associated variants, and trait and pathway-specific GRS to infer possible consequences of intervening in pathways underlying lung function. We highlight new putative causal variants, genes, proteins and pathways, including those targeted by existing drugs. These findings bring us closer to understanding the mechanisms underlying lung function and COPD, and should inform functional genomics experiments and potentially future COPD therapies.
- Published
- 2022
24. Longitudinal effects of prenatal exposure to plastic-derived chemicals and their metabolites on asthma and lung function from childhood into adulthood
- Author
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Rachel E. Foong, Peter Franklin, Francesca Sanna, Graham L. Hall, Peter D. Sly, Eric B. Thorstensen, Dorota A. Doherty, Jeffrey A. Keelan, and Roger J. Hart
- Subjects
Pulmonary and Respiratory Medicine - Abstract
Environmental exposure to phthalates and bisphenol A (BPA), chemicals used in the production of plastics, may increase risk for asthma and allergies. However, little is known about the long-term effects of early life exposure to these compounds. We investigated if prenatal exposure to these compounds was associated with asthma, allergy and lung function outcomes from early childhood into adulthood in a cohort study.Maternal serum samples collected from 846 pregnant women in the Raine Study were assayed for BPA and phthalate metabolites. The children of these women were followed up at 5, 13 and 22 years where spirometry and respiratory questionnaires were conducted to determine asthma and allergy status. Lung function trajectories were derived from longitudinal spirometry measurements. Multinomial logistic regression and weighted quantile sum regression was used to test associations of individual and chemical mixtures with asthma phenotypes and lung function trajectories.Effects of prenatal BPA and phthalates on asthma phenotypes were seen in male offspring, where BPA was associated with increased risk for persistent asthma, while mono-iso-butyl phthalate and mono-iso-decyl phthalate was associated with increased risk for adult asthma. Prenatal BPA had no effect on lung function trajectories, but prenatal phthalate exposure was associated with improved lung function.Prenatal BPA exposure was associated with increased likelihood of persistent asthma in males, while prenatal phthalate exposure was associated with increased likelihood of adult asthma in males. Results suggest that prenatal exposure to prenatal BPA and phthalates affect asthma risk, particularly in males, however lung function was not adversely affected.
- Published
- 2022
25. Lung abnormalities do not influence aerobic capacity in school children born preterm
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Shannon J. Simpson, Graham L. Hall, Christopher O'Dea, Andrew Maiorana, Conor P Murray, Georgia Banton, Karla Logie, Andrew Wilson, and J. Jane Pillow
- Subjects
Spirometry ,Pediatrics ,medicine.medical_specialty ,Physiology ,Population ,03 medical and health sciences ,0302 clinical medicine ,Physiology (medical) ,medicine ,Aerobic exercise ,Orthopedics and Sports Medicine ,education ,Aerobic capacity ,Tidal volume ,education.field_of_study ,Lung ,medicine.diagnostic_test ,business.industry ,Public Health, Environmental and Occupational Health ,030229 sport sciences ,General Medicine ,medicine.disease ,medicine.anatomical_structure ,Bronchopulmonary dysplasia ,Gestation ,business ,030217 neurology & neurosurgery - Abstract
Children born preterm have impaired lung function and altered lung structure. However, there are conflicting reports on how preterm birth impacts aerobic exercise capacity in childhood. We aimed to investigate how neonatal history and a diagnosis of bronchopulmonary dysplasia (BPD) impact the relationship between function and structure of the lung, and aerobic capacity in school-aged children born very preterm. Preterm children (≤ 32 w completed gestation) aged 9–12 years with (n = 38) and without (n = 35) BPD, and term-born controls (n = 31), underwent spirometry, lung volume measurements, gas transfer capacity, a high-resolution computer tomography (CT) scan of the chest, and an incremental treadmill exercise test. Children born preterm with BPD had an elevated breathing frequency to tidal volume ratio compared to term controls (76% vs 63%, p = 0.002). The majority (88%) of preterm children had structural changes on CT scan. There were no differences in peak VO2 (47.1 vs 47.7 mL/kg/min, p = 0.407) or oxygen uptake efficiency slope when corrected for body weight (67.6 vs 67.3, p = 0.5) between preterm children with BPD and term controls. There were no differences in any other exercise outcomes. The severity of structural lung disease was not associated with exercise outcomes in this preterm population. Children born preterm have impaired lung function, and a high prevalence of structural lung abnormalities. However, abnormal lung function and structure do not appear to impact on the aerobic exercise capacity of preterm children at school age.
- Published
- 2020
26. Assessing the importance of Isle of Man waters for the basking shark Cetorhinus maximus
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Graham L. Hall, Haley R. Dolton, Fiona R. Gell, Matthew J. Witt, Lucy A. Hawkes, and Jackie Hall
- Subjects
0106 biological sciences ,Final version ,Ecology ,biology ,010604 marine biology & hydrobiology ,Satellite tracking ,Irish sea ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Basking shark ,lcsh:QK1-989 ,Fishery ,Geography ,lcsh:Botany ,lcsh:Zoology ,Spatial ecology ,lcsh:QL1-991 ,Nature and Landscape Conservation - Abstract
Satellite tracking of endangered or threatened animals can facilitate informed conservation by revealing priority areas for their protection. Basking sharks Cetorhinus maximus (n = 11) were tagged during the summers of 2013, 2015, 2016 and 2017 in the Isle of Man (IoM; median tracking duration 378 d, range: 89-804 d; median minimum straight-line distance travelled 541 km, range: 170-10406 km). Tracking revealed 3 movement patterns: (1) coastal movements within IoM and Irish waters, (2) summer northward movements to Scotland and (3) international movements to Morocco and Norway. One tagged shark was bycaught and released alive in the Celtic Sea. Basking sharks displayed inter-annual site fidelity to the Irish Sea (n = 3), a Marine Nature Reserve (MNR) in IoM waters (n = 1), and Moroccan waters (n = 1). Core distribution areas (50% kernel density estimation) of 5 satellite tracked sharks in IoM waters were compared with 3902 public sightings between 2005 and 2017, highlighting west and south coast hotspots. Location data gathered from satellite tagging broadly correspond to the current boundaries of MNRs in IoM waters. However, minor modifications of some MNR boundaries would incorporate ~20% more satellite tracking location data from this study, and protective measures for basking sharks in IoM waters could further aid conservation of the species at local, regional and international scales. We also show the first documented movement of a basking shark from the British Isles to Norway, and the longest ever track for a tagged basking shark (2 yr and 2 mo, 804 d).
- Published
- 2020
27. ERS/ATS technical standard on interpretive strategies for routine lung function tests
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Sanja Stanojevic, David A. Kaminsky, Martin R. Miller, Bruce Thompson, Andrea Aliverti, Igor Barjaktarevic, Brendan G. Cooper, Bruce Culver, Eric Derom, Graham L. Hall, Teal S. Hallstrand, Joerg D. Leuppi, Neil MacIntyre, Meredith McCormack, Margaret Rosenfeld, and Erik R. Swenson
- Subjects
Pulmonary and Respiratory Medicine ,Spirometry ,Respiratory System ,Medicine and Health Sciences ,Humans ,Lung Volume Measurements ,United States ,Bronchodilator Agents ,Respiratory Function Tests - Abstract
BackgroundAppropriate interpretation of pulmonary function tests (PFTs) involves the classification of observed values as within/outside the normal range based on a reference population of healthy individuals, integrating knowledge of physiological determinants of test results into functional classifications and integrating patterns with other clinical data to estimate prognosis. In 2005, the American Thoracic Society (ATS) and European Respiratory Society (ERS) jointly adopted technical standards for the interpretation of PFTs. We aimed to update the 2005 recommendations and incorporate evidence from recent literature to establish new standards for PFT interpretation.MethodsThis technical standards document was developed by an international joint Task Force, appointed by the ERS/ATS with multidisciplinary expertise in conducting and interpreting PFTs and developing international standards. A comprehensive literature review was conducted and published evidence was reviewed.ResultsRecommendations for the choice of reference equations and limits of normal of the healthy population to identify individuals with unusually low or high results are discussed. Interpretation strategies for bronchodilator responsiveness testing, limits of natural changes over time and severity are also updated. Interpretation of measurements made by spirometry, lung volumes and gas transfer are described as they relate to underlying pathophysiology with updated classification protocols of common impairments.ConclusionsInterpretation of PFTs must be complemented with clinical expertise and consideration of the inherent biological variability of the test and the uncertainty of the test result to ensure appropriate interpretation of an individual's lung function measurements.
- Published
- 2022
28. Addressing Race in Pulmonary Function Testing by Aligning Intent and Evidence With Practice and Perception
- Author
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Graham L. Hall, Christian Bime, David A. Kaminsky, Neeta Thakur, Sanja Stanojevic, Nirav R. Bhakta, and Meredith C. McCormack
- Subjects
Pulmonary and Respiratory Medicine ,Lung Diseases ,media_common.quotation_subject ,Clinical Sciences ,Respiratory System ,Ethnic group ,Black People ,Critical Care and Intensive Care Medicine ,Racism ,White People ,Race (biology) ,pulmonary function test ,Asian People ,Reference Values ,race or ethnicity ,Clinical Research ,Perception ,Ethnicity ,Relevance (law) ,Medicine ,Humans ,Function (engineering) ,Lung ,media_common ,business.industry ,Interpretation (philosophy) ,Racial Groups ,Health Status Disparities ,Health equity ,PFT, pulmonary function test ,Respiratory Function Tests ,Good Health and Well Being ,Spirometry ,Humanities Special Features ,racial disparities ,reference equations ,Respiratory ,Generic health relevance ,Cardiology and Cardiovascular Medicine ,business ,Cognitive psychology - Abstract
The practice of using race or ethnicity in medicine to explain differences between individuals is being called into question because it may contribute to biased medical care and research that perpetuates health disparities and structural racism. A commonly cited example is the use of race or ethnicity in the interpretation of pulmonary function test (PFT) results, yet the perspectives of practicing pulmonologists and physiologists are missing from this discussion. This discussion has global relevance for increasingly multicultural communities in which the range of values that represent normal lung function is uncertain. We review the underlying sources of differences in lung function, including those that may be captured by race or ethnicity, and demonstrate how the current practice of PFT measurement and interpretation is imperfect in its ability to describe accurately the relationship between function and health outcomes. We summarize the arguments against using race-specific equations as well as address concerns about removing race from the interpretation of PFT results. Further, we outline knowledge gaps and critical questions that need to be answered to change the current approach of including race or ethnicity in PFT results interpretation thoughtfully. Finally, we propose changes in interpretation strategies and future research to reduce health disparities.
- Published
- 2022
29. Collecting exhaled breath condensate from non-ventilated preterm-born infants: a modified method
- Author
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Benjamin Stoecklin, Graham L. Hall, Rhea Urs, J. Jane Pillow, Benjamin Hartmann, and Shannon J. Simpson
- Subjects
Pediatrics ,medicine.medical_specialty ,business.industry ,Pediatrics, Perinatology and Child Health ,Pediatric surgery ,medicine ,Modified method ,Exhaled breath condensate ,business - Published
- 2021
30. Real-world application of Spirometry Quality Control Deep-Learning Algorithm
- Author
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Renee Jensen, Wim Janssens, Sanja Stanojevic, Marko Topalovic, Carmen Hernandez, Graham L. Hall, Felip Burgos, Pippa Powell, Kevin Ray, Nilakash Das, Felix Ratjen, and Carlos A. Jiménez-Ruiz
- Subjects
Spirometry ,medicine.diagnostic_test ,business.industry ,Deep learning ,media_common.quotation_subject ,Control (management) ,Machine learning ,computer.software_genre ,Medicine ,Quality (business) ,Artificial intelligence ,business ,computer ,media_common - Published
- 2021
31. Impact of moderate to late preterm birth on 5 year lung function in a South African birth cohort
- Author
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Heather J. Zar, Diane Gray, Zoltán Hantos, Shaakira Chaya, Carvern Jacobs, Rae Macginty, Graham L. Hall, and Shannon J. Simpson
- Subjects
medicine.medical_specialty ,Late Preterm Birth ,Obstetrics ,business.industry ,medicine ,business ,Birth cohort ,Lung function - Published
- 2021
32. Normative multiple-breath washout data in school-aged children corrected for sensor error
- Author
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Anne-Christianne Kentgens, Philipp Latzin, Pinelopi Anagnostopoulou, Renee Jensen, Mirjam Stahl, Alana Harper, Sophie Yammine, Rachel E. Foong, Graham L. Hall, Florian Singer, Sanja Stanojevic, Marcus A. Mall, Felix Ratjen, and Kathryn A. Ramsey
- Subjects
Pulmonary and Respiratory Medicine ,Breath Tests ,Functional Residual Capacity ,Humans ,610 Medicine & health ,Child ,Respiratory Function Tests - Published
- 2021
33. Early life exposure to coal mine fire smoke emissions and altered lung function in young children
- Author
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Graham L. Hall, K Chappell, Michael J. Abramson, Shyamali C. Dharmage, Fay H. Johnston, Shannon M. Melody, Rachel E. Foong, Grant J. Williamson, Jingyi Shao, M Dalton, Tierney O'Sullivan, Amanda J. Wheeler, and Graeme R. Zosky
- Subjects
Male ,Pulmonary and Respiratory Medicine ,preschool children ,Birth weight ,Fires ,Pregnancy ,Interquartile range ,Smoke ,Environmental health ,Linear regression ,Humans ,Medicine ,Prospective Studies ,Prospective cohort study ,long-term effects ,Lung ,Air Pollutants ,business.industry ,outdoor smoke ,respiratory function tests ,Confounding ,Infant ,Infant exposure ,Environmental Exposure ,Environmental exposure ,Coal Mining ,Child, Preschool ,Female ,Particulate Matter ,business - Abstract
BACKGROUND AND OBJECTIVE: Long-term respiratory risks following exposure to relatively short periods of poor air quality early in life are unknown. We aimed to evaluate the association between exposure to a 6-week episode of air pollution from a coal mine fire in children aged
- Published
- 2019
34. Poster Sessions
- Author
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Heather J. Zar, Peter D. Sly, Lauren McMillan, Graham L. Hall, Carvern Jacobs, Rae Macginty, Jacob A M Stadler, Anessa Vanker, Lidija Turkovic, and Diane Gray
- Subjects
Pulmonary and Respiratory Medicine ,business.industry ,Early life ,Tobacco smoke ,Abstracts ,03 medical and health sciences ,0302 clinical medicine ,Indoor air quality ,Environmental health ,Pediatrics, Perinatology and Child Health ,Medicine ,030212 general & internal medicine ,Birth cohort ,business ,030217 neurology & neurosurgery ,Lung function - Published
- 2019
35. Long-term medical and psychosocial outcomes in congenital diaphragmatic hernia survivors
- Author
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Andrew Wilson, Conor P Murray, Naeem Samnakay, Graham L. Hall, Jan E. Dickinson, Georgia Banton, J. Ramsay, Corrado Minutillo, Maureen Verheggen, Jason K Tan, and Elizabeth Nathan
- Subjects
Male ,Vital capacity ,Pediatrics ,medicine.medical_specialty ,Adolescent ,Child Health Services ,Population ,Gestational Age ,Scoliosis ,Pulmonary function testing ,03 medical and health sciences ,0302 clinical medicine ,Quality of life ,Surveys and Questionnaires ,030225 pediatrics ,medicine ,Humans ,Survivors ,Child ,education ,education.field_of_study ,business.industry ,Congenital diaphragmatic hernia ,Western Australia ,Strengths and Difficulties Questionnaire ,medicine.disease ,Respiratory Function Tests ,030228 respiratory system ,Echocardiography ,Case-Control Studies ,Pediatrics, Perinatology and Child Health ,Quality of Life ,Female ,Hernias, Diaphragmatic, Congenital ,Tomography, X-Ray Computed ,business ,Psychosocial - Abstract
ObjectiveSurvival rates for congenital diaphragmatic hernia (CDH) are increasing. The long-term outcomes of CDH survivors were compared with a healthy control group to assess the morbidity for guidance of antenatal counselling and long-term follow-up programmes.Participants and designParticipants born with CDH in Western Australia 1993–2008 were eligible with matched controls from the general population. Participants had comprehensive lung function tests, echocardiogram, low-dose chest CT scan and completed a Strengths and Difficulties Questionnaire (SDQ) and quality of life (QOL) questionnaire.Results34 matched case–control pairs were recruited. Demographic data between groups were similar. Cases were smaller at follow-up (weight Z-score of −0.2vs0.3; p=0.03; height Z-score of −0.3vs0.6; p=0.01). Cases had lower mean Z-scores for forced expiratory volume in 1 s (FEV1) (−1.49 vs −0.01; p=0.004), FEV1/forced vital capacity (−1.92 vs −1.2; p=0.009) and forced expiratory flow at 25-75% (FEF25-75) (−1.18vs0.23; p=0.007). Cases had significantly worse respiratory mechanics using forced oscillation technique. Subpleural triangles architectural distortion, linear opacities and scoliosis on chest CT were significantly higher in cases. Prosthetic patch requirement was associated with worse lung mechanics and peak cough flow. Cases had significantly higher rates of gastro-oesophageal reflux disease (GORD) and GORD medication usage. Developmental delay was significantly higher in cases. More cases had a total difficulties score in the high to very high range (25% vs 0%, p=0.03) on the SDQ and reported lower objective QOL scores (70.2 vs 79.8, p=0.02).ConclusionSurvivors of CDH may have significant adverse long-term medical and psychosocial issues that would be better recognised and managed in a multidisciplinary clinic.
- Published
- 2019
36. Single‐breath washout and association with structural lung disease in children with cystic fibrosis
- Author
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Sarath Ranganathan, Sophie Yammine, Graham L. Hall, Billy Skoric, Philipp Latzin, Louise King, Tim Rosenow, and Kathryn A. Ramsey
- Subjects
Male ,Pulmonary and Respiratory Medicine ,Adolescent ,Cystic Fibrosis ,Functional Residual Capacity ,Lung Clearance Index ,Air trapping ,Cystic fibrosis ,03 medical and health sciences ,0302 clinical medicine ,Functional residual capacity ,030225 pediatrics ,medicine ,Humans ,Lung Diseases, Obstructive ,Prospective Studies ,Child ,Prospective cohort study ,Lung ,Bronchiectasis ,business.industry ,medicine.disease ,Respiratory Function Tests ,Cross-Sectional Studies ,medicine.anatomical_structure ,Breath Tests ,030228 respiratory system ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,Breathing ,Female ,medicine.symptom ,Pulmonary Ventilation ,Tomography, X-Ray Computed ,business ,Nuclear medicine - Abstract
Background In children with cystic fibrosis (CF) lung clearance index (LCI) from multiple-breath washout (MBW) correlates with structural lung disease. As a shorter test, single-breath washout (SBW) represents an attractive alternative to assess the ventilation distribution, however, data for the correlation with lung imaging are lacking. Methods We assessed correlations between phase III slope (SIII) of double-tracer gas SBW, nitrogen MBW indices (LCI and moment ratios for overall ventilation distribution, Scond, and Sacin for conductive and mainly acinar ventilation, respectively) and structural lung disease assessed by chest computed tomography (CT) in children with CF. Results In a prospective cross-sectional study data from MBW, SBW, and chest CT were obtained in 32 children with CF with a median (range) age of 8.2 (5.2-16.3) years. Bronchiectasis was present in 24 (75%) children and air trapping was present in 29 (91%). Median (IQR) SIII of SBW was -138.4 (150.6) mg/mol. We found no association between SIII with either the MBW outcomes or CT scores (n = 23, association with bronchiectasis extent r = 0.10, P = 0.64). LCI and Scond were associated with bronchiectasis extent (n = 23, r = 0.57, P = 0.004; r = 0.60, P = 0.003, respectively). Conclusions Acinar ventilation inhomogeneity measured by SBW was not associated with structural lung disease on CT. Double-tracer SBW added no benefit to indices measured by MBW.
- Published
- 2019
37. Does machine learning have a role in the prediction of asthma in children?
- Author
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André Schultz, Rachel E. Foong, Graham L. Hall, Dimpalben Patel, Anne Smith, and David Broadhurst
- Subjects
Pulmonary and Respiratory Medicine ,Childhood asthma ,business.industry ,Machine learning ,computer.software_genre ,medicine.disease ,Predictive value ,Asthma ,Machine Learning ,03 medical and health sciences ,0302 clinical medicine ,030228 respiratory system ,Lung disease ,Pediatrics, Perinatology and Child Health ,medicine ,Humans ,030212 general & internal medicine ,Artificial intelligence ,business ,Child ,computer - Abstract
Asthma is the most common chronic lung disease in childhood. There has been a significant worldwide effort to develop tools/methods to identify children’s risk for asthma as early as possible for preventative and early management strategies. Unfortunately, most childhood asthma prediction tools using conventional statistical models have modest accuracy, sensitivity, and positive predictive value. Machine learning is an approach that may improve on conventional models by finding patterns and trends from large and complex datasets. Thus far, few studies have utilized machine learning to predict asthma in children. This review aims to critically assess these studies, describe their limitations, and discuss future directions to move from proof-of-concept to clinical application.
- Published
- 2021
38. Variants associated with HHIP expression have sex-differential effects on lung function
- Author
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Carl A. Melbourne, Caroline Hayward, Stefan Karrasch, Dirk Keidel, Katherine A. Fawcett, Susan M. Ring, Yohan Bossé, Carol A. Wang, Ben Michael Brumpton, Claudia Langenberg, Peter K. Joshi, Ke Hao, Igor Rudan, David J. Porteous, Don D. Sin, Raquel Granell, Blair H. Smith, Jian'an Luan, Kristian Hveem, Sarah E. Harris, Sandosh Padmanabhan, Archie Campbell, Sebastian May-Wilson, Veronique Vitart, Nicola Pirastu, Arnulf Langhammer, Craig E. Pennell, John M. Starr, Stefan Weiss, Karina Patasova, Nicholas J. Wareham, James F. Wilson, Deborah Jarvis, Tim D. Spector, Nick Shrine, David P. Strachan, Martin D. Tobin, Beate Stubbe, David M. Evans, Kirsi H. Pietiläinen, Mangino Massimo, Ian P. Hall, Graham L. Hall, Jaakko Kaprio, Ralf Ewert, Rachel E. Foong, Claudia Flexeder, Louise V. Wain, Ma'en Obeidat, Cristen J. Willer, Leo-Pekka Lyytikäinen, Olli T. Raitakari, John Henderson, Konstantin Strauch, Marta R Moksnes, Cosetta Minelli, Nicole Probst-Hensch, Pirro G. Hysi, Anna L. Guyatt, Henry Völzke, Thomas Meitinger, Peter D. Sly, Ozren Polasek, Anne Richmond, Mika Kähönen, Maarten van den Berge, Medea Imboden, Thibaud Boutin, Lucija Klaric, Laura Portas, Terho Lehtimäki, Ian J. Deary, Taina Rantanen, Catherine John, Teemu Palviainen, Fawcett, Katherine A [0000-0002-6675-2112], Obeidat, Ma'en [0000-0002-5443-2752], Shrine, Nick [0000-0003-3641-4371], Weiss, Stefan [0000-0002-3553-4315], May-Wilson, Sebastian [0000-0003-2668-5717], Boutin, Thibaud S [0000-0003-4754-1675], Portas, Laura [0000-0003-1789-1893], Harris, Sarah E [0000-0002-4941-5106], Lyytikäinen, Leo-Pekka [0000-0002-7200-5455], Palviainen, Teemu [0000-0002-7847-8384], Keidel, Dirk [0000-0003-4706-5728], Minelli, Cosetta [0000-0001-9166-3958], Langenberg, Claudia [0000-0002-5017-7344], Bossé, Yohan [0000-0002-3067-3711], Van den Berge, Maarten [0000-0002-9336-7340], Sin, Don D [0000-0002-0756-6643], Campbell, Archie [0000-0003-0198-5078], Porteous, David [0000-0003-1249-6106], Padmanabhan, Sandosh [0000-0003-3869-5808], Smith, Blair H [0000-0002-5362-9430], Ring, Sue [0000-0003-3103-9330], Rantanen, Taina [0000-0002-1604-1945], Pennell, Craig E [0000-0002-0937-6165], Kaprio, Jaakko [0000-0002-3716-2455], Vitart, Veronique [0000-0002-4991-3797], Hayward, Caroline [0000-0002-9405-9550], Hall, Ian P [0000-0001-9933-3216], Wain, Louise V [0000-0003-4951-1867], Apollo - University of Cambridge Repository, Groningen Research Institute for Asthma and COPD (GRIAC), Technology Centre, University of Helsinki, Institute for Molecular Medicine Finland, Genetic Epidemiology, HUS Abdominal Center, Department of Medicine, Clinicum, CAMM - Research Program for Clinical and Molecular Metabolism, Department of Public Health, Research Programs Unit, Tampere University, Clinical Medicine, Department of Clinical Chemistry, TAYS Heart Centre, and Department of Clinical Physiology and Nuclear Medicine
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0301 basic medicine ,Spirometry ,medicine.medical_specialty ,HHIP ,Medicine (miscellaneous) ,Expression ,Genome-wide Interaction Study ,Hhip ,Lung Function ,Sex ,Single-nucleotide polymorphism ,Biology ,3121 Internal medicine ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,0302 clinical medicine ,Genome-wide interaction study ,Lung function ,Internal medicine ,expression ,medicine ,sex ,Allele ,Enhancer ,Gene ,Lung ,genome-wide interaction study ,medicine.diagnostic_test ,1184 Genetics, developmental biology, physiology ,lung function ,ALSPAC ,Differential effects ,030104 developmental biology ,Endocrinology ,medicine.anatomical_structure ,030228 respiratory system ,3121 General medicine, internal medicine and other clinical medicine ,3111 Biomedicine - Abstract
Background: Lung function is highly heritable and differs between the sexes throughout life. However, little is known about sex-differential genetic effects on lung function. We aimed to conduct the first genome-wide genotype-by-sex interaction study on lung function to identify genetic effects that differ between males and females. Methods: We tested for interactions between 7,745,864 variants and sex on spirometry-based measures of lung function in UK Biobank (N=303,612), and sought replication in 75,696 independent individuals from the SpiroMeta consortium. Results: Five independent single-nucleotide polymorphisms (SNPs) showed genome-wide significant (P-8) interactions with sex on lung function, and 21 showed suggestive interactions (P-6). The strongest signal, from rs7697189 (chr4:145436894) on forced expiratory volume in 1 second (FEV1) (P=3.15x10-15), was replicated (P=0.016) in SpiroMeta. The C allele increased FEV1 more in males (untransformed FEV1 β=0.028 [SE 0.0022] litres) than females (β=0.009 [SE 0.0014] litres), and this effect was not accounted for by differential effects on height, smoking or pubertal age. rs7697189 resides upstream of the hedgehog-interacting protein (HHIP) gene and was previously associated with lung function and HHIP lung expression. We found HHIP expression was significantly different between the sexes (P=6.90x10-6), but we could not detect sex differential effects of rs7697189 on expression. Conclusions: We identified a novel genotype-by-sex interaction at a putative enhancer region upstream of the HHIP gene. Establishing the mechanism by which HHIP SNPs have different effects on lung function in males and females will be important for our understanding of lung health and diseases in both sexes.
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- 2021
39. Associations between respiratory and vascular function in early childhood
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Shyamali C. Dharmage, Shannon M. Melody, Michael J. Abramson, Grant J. Williamson, Rachel E. Foong, K Chappell, M Dalton, Emily J Hemstock, Fay H. Johnston, Amanda J. Wheeler, Jingyi Shao, Graeme R. Zosky, Bing Zhao, Kazuaki Negishi, and Graham L. Hall
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Pulmonary and Respiratory Medicine ,Adult ,medicine.medical_specialty ,Pulse Wave Analysis ,Carotid Intima-Media Thickness ,smoking ,Fires ,Pulmonary function testing ,vascular function ,respiratory function ,Pregnancy ,Internal medicine ,Medicine ,early life ,Humans ,Respiratory function ,Prospective Studies ,Respiratory system ,Prospective cohort study ,Child ,Pulse wave velocity ,Lung ,business.industry ,Cardiorespiratory fitness ,medicine.disease ,maternal education ,medicine.anatomical_structure ,Child, Preschool ,Cardiology ,Arterial stiffness ,Female ,Particulate Matter ,business - Abstract
Background and objective: The link between respiratory and vascular health is well documented in adult populations. Impaired lung function is consistently associated with thicker arteries and higher incidence of cardiovascular disease. However, there are limited data on this relationship in young children and the studies that exist have focussed on populations at high risk of cardiorespiratory morbidity. We determined if an association exists between respiratory and cardiovascular function in young children and, if so, whether it is confounded by known cardiorespiratory risk factors. Methods: Respiratory and vascular data from a prospective cohort study established to evaluate the health implications 3 years after coal mine fire smoke exposure in children aged 3–5 years were used. Respiratory function was measured using the forced oscillation technique and included resistance at 5 Hz (R5), reactance at 5 Hz (X5) and area under the reactance curve (AX). Vascular health was measured by carotid intima-media thickness (ultrasound) and pulse wave velocity (arterial tonometry). Regression analyses were used to examine the relationship between the respiratory Z-scores and cardiovascular measures. Subsequent analyses were adjusted for potential confounding by maternal smoking during pregnancy, maternal education and exposure to fine particulate matter Results: Peripheral lung function (X5 and AX), but not respiratory system resistance (R5), was associated with vascular function. Adjustment for maternal smoking, maternal education and early life exposure to PM2.5 had minimal effect on these associations. Conclusion: These observations suggest that peripheral lung stiffness is associated with vascular stiffness and that this relationship is established early in life.
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- 2021
40. Author reply: Do Tunisians have a European ancestry?
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Tolu Okitika, Nicole Filipow, Sanja Stanojevic, Gregg L Ruppel, Irene Steenbruggen, Graham L. Hall, Bruce Thompson, Jane Kirkby, and Brendan G Cooper
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Pulmonary and Respiratory Medicine ,Haplotypes ,business.industry ,Medicine ,Black People ,Humans ,business ,Genealogy ,Bit (key) - Abstract
Until we have more comprehensive data from all regions in the world, we must be careful not to apply GLI equations indiscriminatelyhttps://bit.ly/3g1r9Q5
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- 2021
41. Forced oscillation techniques
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Shannon J. Simpson, Sherlynn Ang, and Graham L. Hall
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- 2021
42. Pulmonary function testing in infants and preschool children
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Enrico Lombardi, Graham L. Hall, and Claudia Calogero
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- 2021
43. Assessing respiratory risks of air travel, altitude and diving
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Graham L. Hall, Carly Seeber, and Mary Sharp
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Altitude ,Meteorology ,business.industry ,Medicine ,Respiratory system ,business ,Air travel - Published
- 2021
44. Lung inflammation and simulated airway resistance in infants with cystic fibrosis
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AREST CF, Emily M. DeBoer, Julia S. Kimbell, Kaci Pickett, Joseph E. Hatch, Kathryn Akers, John Brinton, Graham L. Hall, Louise King, Fiona Ramanauskas, Tim Rosenow, S Stick, H.A.W.M. Tiddens, Thomas W. Ferkol, Sarath C. Ranganathan, Stephanie D. Davis, AREST CF, Emily M. DeBoer, Julia S. Kimbell, Kaci Pickett, Joseph E. Hatch, Kathryn Akers, John Brinton, Graham L. Hall, Louise King, Fiona Ramanauskas, Tim Rosenow, S Stick, H.A.W.M. Tiddens, Thomas W. Ferkol, Sarath C. Ranganathan, and Stephanie D. Davis
- Abstract
Cystic fibrosis (CF) is characterized by small airway disease; but central airways may also be affected. We hypothesized that airway resistance estimated from computational fluid dynamic (CFD) methodology in infants with CF was higher than controls and that early airway inflammation in infants with CF is associated with airway resistance. Central airway models with a median of 51 bronchial outlets per model (interquartile range 46,56) were created from chest computed tomography scans of 18 infants with CF and 7 controls. Steady state airflow into the trachea was simulated to estimate central airway resistance in each model. Airway resistance was increased in the full airway models of infants with CF versus controls and in models trimmed to 33 bronchi. Airway resistance was associated with markers of inflammation in bronchoalveolar lavage fluid obtained approximately 8 months earlier but not with markers obtained at the same time. In conclusion, airway resistance estimated by CFD modeling is increased in infants with CF compared to controls and may be related to early airway inflammation.
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- 2021
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45. Collecting exhaled breath condensate from non-ventilated preterm-born infants: a modified method
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Rhea, Urs, Benjamin, Stoecklin, J Jane, Pillow, Benjamin, Hartmann, Graham L, Hall, and Shannon J, Simpson
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Breath Tests ,Exhalation ,Infant, Newborn ,Humans ,Infant ,Biomarkers ,Infant, Premature - Published
- 2020
46. Characterization of lung function trajectories in the Raine Study
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Peter D. Sly, Graham L. Hall, Francesca Locatelli, Elisha White, Rachel E. Foong, and Francesca Sanna
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Pathology ,medicine.medical_specialty ,medicine ,Biology ,Lung function ,Characterization (materials science) - Published
- 2020
47. Intra-breath and spectral oscillometry in preterm-born children
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Graham L. Hall, Denby J. Evans, Shannon J. Simpson, and Rhea Urs
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medicine.medical_specialty ,business.industry ,Internal medicine ,medicine ,Cardiology ,Oscillometry ,business - Published
- 2020
48. Cohort Profile: The Hazelwood Health Study Latrobe Early Life Follow-Up (ELF) Study
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Shannon M. Melody, Martine Dennekamp, Rachel E. Foong, Fay H. Johnston, Alison Venn, M Dalton, Shyamali C. Dharmage, Jane B. Ford, Bing Zhao, K Chappell, Jillian Ikin, Grant J. Williamson, Karen Wills, Kazuaki Negishi, Michael J. Abramson, Melanie Reeves, Judi Walker, Gabriela A. Willis, Graham L. Hall, Jingyi Shao, Amanda J. Wheeler, Kathryn M. Emmerson, and Graeme R. Zosky
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Smoke ,Epidemiology ,business.industry ,Coal mining ,Air pollution ,Attendance ,General Medicine ,medicine.disease_cause ,Cohort Studies ,Geography ,Environmental health ,Health care ,Cohort ,medicine ,Humans ,Early childhood ,business ,Cohort study ,Follow-Up Studies - Abstract
The Hazelwood coal mine fire in Victoria, Australia, was an unprecedented national outdoor air pollution event that covered the surrounding area in smoke and ash for 6 weeks in February and March 2014 (Figure 1). The severe smoke event caused considerable community concerns within the neighbouring town of Morwell and the broader Latrobe Valley community, situated 150 km east of the capital city of Melbourne. The Latrobe Valley is a regional setting known for mining and agricultural industries, characterised by relative socioeconomic disadvantage compared with the rest of the state. In response to these concerns, and following extensive community consultation, the Hazelwood Health Study was established to examine the long-term impacts of the mine fire (https://hazelwoodhealthstudy.org.au/). The Hazelwood Health Study involves multiple research streams focusing on various health outcomes and vulnerable groups. The Latrobe Early Life Follow-up (ELF) Study is a stream of the Hazelwood Health Study which aims to investigate the potential impacts of exposure to a severe outdoor air pollution event, as caused by the 2014 Hazelwood coal mine fire, on the health and development of children in the Latrobe Valley. Specific objectives are to explore: (i) obstetric and perinatal outcomes; (ii) parental reports of minor illnesses in young children; (iii) respiratory, vascular and immune function of children from 3 to 12 years of age; and (iv) medication use, health care attendance, education and developmental outcomes in childhood following in utero and early childhood exposure to smoke from the Hazelwood coal mine fire. We also aim to evaluate whether the persistence of smoke and ash pollutants in homes is a useful additional marker of exposure to mine fire emissions. Ethics statement Ethics approval was obtained from the Tasmania Health and Medical Human Research Ethics Committee (ref H0015033 and H0014875).
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- 2020
49. Lung abnormalities do not influence aerobic capacity in school children born preterm
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Christopher A, O'Dea, Karla, Logie, Andrew C, Wilson, J Jane, Pillow, Conor, Murray, Georgia, Banton, Shannon J, Simpson, Graham L, Hall, and Andrew, Maiorana
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Male ,Exercise Tolerance ,Schools ,Respiration ,Spirometry ,Exercise Test ,Tidal Volume ,Humans ,Premature Birth ,Female ,Child ,Exercise ,Lung ,Bronchopulmonary Dysplasia - Abstract
Children born preterm have impaired lung function and altered lung structure. However, there are conflicting reports on how preterm birth impacts aerobic exercise capacity in childhood. We aimed to investigate how neonatal history and a diagnosis of bronchopulmonary dysplasia (BPD) impact the relationship between function and structure of the lung, and aerobic capacity in school-aged children born very preterm.Preterm children (≤ 32 w completed gestation) aged 9-12 years with (n = 38) and without (n = 35) BPD, and term-born controls (n = 31), underwent spirometry, lung volume measurements, gas transfer capacity, a high-resolution computer tomography (CT) scan of the chest, and an incremental treadmill exercise test.Children born preterm with BPD had an elevated breathing frequency to tidal volume ratio compared to term controls (76% vs 63%, p = 0.002). The majority (88%) of preterm children had structural changes on CT scan. There were no differences in peak V̇OChildren born preterm have impaired lung function, and a high prevalence of structural lung abnormalities. However, abnormal lung function and structure do not appear to impact on the aerobic exercise capacity of preterm children at school age.
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- 2020
50. High resolution biologging of breaching by the world's second largest shark species
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Graham L. Hall, S. M. Henderson, Matthew J. Witt, Owen M. Exeter, Jessica L. Rudd, Christopher Kerry, Jackie Hall, and Lucy A. Hawkes
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0106 biological sciences ,Behavioural ecology ,Science ,Endangered species ,High resolution ,Ecological succession ,010603 evolutionary biology ,01 natural sciences ,Article ,Animals ,Biomechanics ,Atlantic Ocean ,Multidisciplinary ,Behavior, Animal ,Conservation biology ,010604 marine biology & hydrobiology ,Energetics ,Logging ,Endangered Species ,Plankton ,Biooceanography ,Fishery ,Geography ,Seafood ,Sharks ,%22">Fish ,Medicine - Abstract
Basking sharks, the world’s second largest fish, are endangered globally following two centuries of large-scale exploitation for their oily livers. In the northeast Atlantic, they seasonally gather in key sites, including the western Scottish Isles, where they feed on plankton, but their breeding grounds are currently completely unknown. Using high-resolution three-axis accelerometry and depth logging, we present the first direct records of breaching by basking sharks over 41 days. We show that basking sharks breach both during the night and day, starting at approximately 20 m depth and can breach multiple times in short succession. We also present early evidence of potential lateralisation in basking sharks. Given the energetic nature of breaching, it should have an important biological function, but this remains unclear.
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- 2020
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