18 results on '"Sternby, H."'
Search Results
2. Pancreatic Enzyme Replacement Therapy Influences Survival in Patients with Incurable Pancreatic Cancer
- Author
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Sternby, H., primary and Tingstedt, B., additional
- Published
- 2023
- Full Text
- View/download PDF
3. Lifetime alcohol intake, drinking patterns over time and risk of stomach cancer: A pooled analysis of data from two prospective cohort studies
- Author
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Jayasekara, H. MacInnis, R.J. Lujan-Barroso, L. Mayen-Chacon, A.-L. Cross, A.J. Wallner, B. Palli, D. Ricceri, F. Pala, V. Panico, S. Tumino, R. Kühn, T. Kaaks, R. Tsilidis, K. Sánchez, M.-J. Amiano, P. Ardanaz, E. Chirlaque López, M.D. Merino, S. Rothwell, J.A. Boutron-Ruault, M.-C. Severi, G. Sternby, H. Sonestedt, E. Bueno-de-Mesquita, B. Boeing, H. Travis, R. Sandanger, T.M. Trichopoulou, A. Karakatsani, A. Peppa, E. Tjønneland, A. Yang, Y. Hodge, A.M. Mitchell, H. Haydon, A. Room, R. Hopper, J.L. Weiderpass, E. Gunter, M.J. Riboli, E. Giles, G.G. Milne, R.L. Agudo, A. English, D.R. Ferrari, P.
- Abstract
Alcohol consumption is causally linked to several cancers but the evidence for stomach cancer is inconclusive. In our study, the association between long-term alcohol intake and risk of stomach cancer and its subtypes was evaluated. We performed a pooled analysis of data collected at baseline from 491 714 participants in the European Prospective Investigation into Cancer and Nutrition and the Melbourne Collaborative Cohort Study. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated for incident stomach cancer in relation to lifetime alcohol intake and group-based life course intake trajectories, adjusted for potential confounders including Helicobacter pylori infection. In all, 1225 incident stomach cancers (78% noncardia) were diagnosed over 7 094 637 person-years; 984 in 382 957 study participants with lifetime alcohol intake data (5 455 507 person-years). Although lifetime alcohol intake was not associated with overall stomach cancer risk, we observed a weak positive association with noncardia cancer (HR = 1.03, 95% CI: 1.00-1.06 per 10 g/d increment), with a HR of 1.50 (95% CI: 1.08-2.09) for ≥60 g/d compared to 0.1 to 4.9 g/d. A weak inverse association with cardia cancer (HR = 0.93, 95% CI: 0.87-1.00) was also observed. HRs of 1.48 (95% CI: 1.10-1.99) for noncardia and 0.51 (95% CI: 0.26-1.03) for cardia cancer were observed for a life course trajectory characterized by heavy decreasing intake compared to light stable intake (Phomogeneity =.02). These associations did not differ appreciably by smoking or H pylori infection status. Limiting alcohol use during lifetime, particularly avoiding heavy use during early adulthood, might help prevent noncardia stomach cancer. Heterogeneous associations observed for cardia and noncardia cancers may indicate etiologic differences. © 2021 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
- Published
- 2021
4. Lifetime alcohol intake, drinking patterns over time and risk of stomach cancer: A pooled analysis of data from two prospective cohort studies.
- Author
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Jayasekara H., MacInnis R.J., Lujan-Barroso L., Mayen-Chacon A.-L., Cross A.J., Wallner B., Palli D., Ricceri F., Pala V., Panico S., Tumino R., Kuhn T., Kaaks R., Tsilidis K., Sanchez M.-J., Amiano P., Ardanaz E., Chirlaque Lopez M.D., Merino S., Rothwell J.A., Boutron-Ruault M.-C., Severi G., Sternby H., Sonestedt E., Bueno-de-Mesquita B., Boeing H., Travis R., Sandanger T.M., Trichopoulou A., Karakatsani A., Peppa E., Tjonneland A., Yang Y., Hodge A.M., Mitchell H., Haydon A., Room R., Hopper J.L., Weiderpass E., Gunter M.J., Riboli E., Giles G.G., Milne R.L., Agudo A., English D.R., Ferrari P., Jayasekara H., MacInnis R.J., Lujan-Barroso L., Mayen-Chacon A.-L., Cross A.J., Wallner B., Palli D., Ricceri F., Pala V., Panico S., Tumino R., Kuhn T., Kaaks R., Tsilidis K., Sanchez M.-J., Amiano P., Ardanaz E., Chirlaque Lopez M.D., Merino S., Rothwell J.A., Boutron-Ruault M.-C., Severi G., Sternby H., Sonestedt E., Bueno-de-Mesquita B., Boeing H., Travis R., Sandanger T.M., Trichopoulou A., Karakatsani A., Peppa E., Tjonneland A., Yang Y., Hodge A.M., Mitchell H., Haydon A., Room R., Hopper J.L., Weiderpass E., Gunter M.J., Riboli E., Giles G.G., Milne R.L., Agudo A., English D.R., and Ferrari P.
- Abstract
Alcohol consumption is causally linked to several cancers but the evidence for stomach cancer is inconclusive. In our study, the association between long-term alcohol intake and risk of stomach cancer and its subtypes was evaluated. We performed a pooled analysis of data collected at baseline from 491 714 participants in the European Prospective Investigation into Cancer and Nutrition and the Melbourne Collaborative Cohort Study. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated for incident stomach cancer in relation to lifetime alcohol intake and group-based life course intake trajectories, adjusted for potential confounders including Helicobacter pylori infection. In all, 1225 incident stomach cancers (78% noncardia) were diagnosed over 7 094 637 person-years; 984 in 382 957 study participants with lifetime alcohol intake data (5 455 507 person-years). Although lifetime alcohol intake was not associated with overall stomach cancer risk, we observed a weak positive association with noncardia cancer (HR = 1.03, 95% CI: 1.00-1.06 per 10 g/d increment), with a HR of 1.50 (95% CI: 1.08-2.09) for >=60 g/d compared to 0.1 to 4.9 g/d. A weak inverse association with cardia cancer (HR = 0.93, 95% CI: 0.87-1.00) was also observed. HRs of 1.48 (95% CI: 1.10-1.99) for noncardia and 0.51 (95% CI: 0.26-1.03) for cardia cancer were observed for a life course trajectory characterized by heavy decreasing intake compared to light stable intake (Phomogeneity =.02). These associations did not differ appreciably by smoking or H pylori infection status. Limiting alcohol use during lifetime, particularly avoiding heavy use during early adulthood, might help prevent noncardia stomach cancer. Heterogeneous associations observed for cardia and noncardia cancers may indicate etiologic differences.Copyright © 2021 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
- Published
- 2021
5. Lifetime alcohol intake, drinking patterns over time and risk of stomach cancer: A pooled analysis of data from two prospective cohort studies
- Author
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Jayasekara, H, MacInnis, RJ, Lujan-Barroso, L, Mayen-Chacon, A-L, Cross, AJ, Wallner, B, Palli, D, Ricceri, F, Pala, V, Panico, S, Tumino, R, Kuehn, T, Kaaks, R, Tsilidis, K, Sanchez, M-J, Amiano, P, Ardanaz, E, Chirlaque Lopez, MD, Merino, S, Rothwell, JA, Boutron-Ruault, M-C, Severi, G, Sternby, H, Sonestedt, E, Bueno-de-Mesquita, B, Boeing, H, Travis, R, Sandanger, TM, Trichopoulou, A, Karakatsani, A, Peppa, E, Tjonneland, A, Yang, Y, Hodge, AM, Mitchell, H, Haydon, A, Room, R, Hopper, JL, Weiderpass, E, Gunter, MJ, Riboli, E, Giles, GG, Milne, RL, Agudo, A, English, DR, Ferrari, P, Jayasekara, H, MacInnis, RJ, Lujan-Barroso, L, Mayen-Chacon, A-L, Cross, AJ, Wallner, B, Palli, D, Ricceri, F, Pala, V, Panico, S, Tumino, R, Kuehn, T, Kaaks, R, Tsilidis, K, Sanchez, M-J, Amiano, P, Ardanaz, E, Chirlaque Lopez, MD, Merino, S, Rothwell, JA, Boutron-Ruault, M-C, Severi, G, Sternby, H, Sonestedt, E, Bueno-de-Mesquita, B, Boeing, H, Travis, R, Sandanger, TM, Trichopoulou, A, Karakatsani, A, Peppa, E, Tjonneland, A, Yang, Y, Hodge, AM, Mitchell, H, Haydon, A, Room, R, Hopper, JL, Weiderpass, E, Gunter, MJ, Riboli, E, Giles, GG, Milne, RL, Agudo, A, English, DR, and Ferrari, P
- Abstract
Alcohol consumption is causally linked to several cancers but the evidence for stomach cancer is inconclusive. In our study, the association between long-term alcohol intake and risk of stomach cancer and its subtypes was evaluated. We performed a pooled analysis of data collected at baseline from 491 714 participants in the European Prospective Investigation into Cancer and Nutrition and the Melbourne Collaborative Cohort Study. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated for incident stomach cancer in relation to lifetime alcohol intake and group-based life course intake trajectories, adjusted for potential confounders including Helicobacter pylori infection. In all, 1225 incident stomach cancers (78% noncardia) were diagnosed over 7 094 637 person-years; 984 in 382 957 study participants with lifetime alcohol intake data (5 455 507 person-years). Although lifetime alcohol intake was not associated with overall stomach cancer risk, we observed a weak positive association with noncardia cancer (HR = 1.03, 95% CI: 1.00-1.06 per 10 g/d increment), with a HR of 1.50 (95% CI: 1.08-2.09) for ≥60 g/d compared to 0.1 to 4.9 g/d. A weak inverse association with cardia cancer (HR = 0.93, 95% CI: 0.87-1.00) was also observed. HRs of 1.48 (95% CI: 1.10-1.99) for noncardia and 0.51 (95% CI: 0.26-1.03) for cardia cancer were observed for a life course trajectory characterized by heavy decreasing intake compared to light stable intake (Phomogeneity = .02). These associations did not differ appreciably by smoking or H pylori infection status. Limiting alcohol use during lifetime, particularly avoiding heavy use during early adulthood, might help prevent noncardia stomach cancer. Heterogeneous associations observed for cardia and noncardia cancers may indicate etiologic differences.
- Published
- 2021
6. No difference in complication rate after neoadjuvant chemotherapy versus upfront pancreatic surgery - a review of the Swedish National Pancreatic and Periampullary cancer Registry
- Author
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Sternby, H., primary and Andersson, B., additional
- Published
- 2020
- Full Text
- View/download PDF
7. Determinants of Severity in Acute Pancreatitis
- Author
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Sternby H, Bolado F, Canaval-Zuleta HJ, Marra-López C, Hernando-Alonso AI, Del-Val-Antoñana A, García-Rayado G, Rivera-Irigoin R, Grau-García FJ, Oms L, Millastre-Bocos J, Pascual-Moreno I, Martínez-Ares D, Rodríguez-Oballe JA, López-Serrano A, Ruiz-Rebollo ML, Viejo-Almanzor A, González-de-la-Higuera B, Orive-Calzada A, Gómez-Anta I, Pamies-Guilabert J, Fernández-Gutiérrez-Del-Álamo F, Iranzo-González-Cruz I, Pérez-Muñante ME, Esteba MD, Pardillos-Tomé A, Zapater P, and De madaria E
- Abstract
Objective: The aim of this study was to compare and validate the different classifications of severity in acute pancreatitis (AP) and to investigate which characteristics of the disease are associated with worse outcomes. Summary of Background Data: AP is a heterogeneous disease, ranging from uneventful cases to patients with considerable morbidity and high mortality rates. Severity classifications based on legitimate determinants of severity are important to correctly describe the course of disease. Methods: A prospective multicenter cohort study involving patients with AP from 23 hospitals in Spain. The Atlanta Classification (AC), Revised Atlanta Classification (RAC), and Determinant-based Classification (DBC) were compared. Binary logistic multivariate analysis was performed to investigate independent determinants of severity. Results: A total of 1655 patients were included; 70 patients (4.2%) died. RAC and DBC were equally superior to AC for describing the clinical course of AP. Although any kind of organ failure was associated with increased morbidity and mortality, persistent organ failure (POF) was the most significant determinant of severity. All local complications were associated with worse outcomes. Infected pancreatic necrosis correlated with high morbidity, but in the presence of POF, it was not associated to higher mortality when compared with sterile necrotizing pancreatitis. Exacerbation of previous comorbidity was associated with increased morbidity and mortality. Conclusion: The RAC and DBC both signify an advance in the description and differentiation of AP patients. Herein, we describe the complications of the disease independently associated to morbidity and mortality. Our findings are valuable not only when designing future studies on AP but also for the improvement of current classifications.
- Published
- 2019
8. Lifetime and baseline alcohol intakes and risk of pancreatic cancer in the European Prospective Investigation into Cancer and Nutrition study
- Author
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Naudin, S. Li, K. Jaouen, T. Assi, N. Kyrø, C. Tjønneland, A. Overvad, K. Boutron-Ruault, M.-C. Rebours, V. Védié, A.-L. Boeing, H. Kaaks, R. Katzke, V. Bamia, C. Naska, A. Trichopoulou, A. Berrino, F. Tagliabue, G. Palli, D. Panico, S. Tumino, R. Sacerdote, C. Peeters, P.H. Bueno-de-Mesquita, H.B. Weiderpass, E. Gram, I.T. Skeie, G. Chirlaque, M.-D. Rodríguez-Barranco, M. Barricarte, A. Quirós, J.R. Dorronsoro, M. Johansson, I. Sund, M. Sternby, H. Bradbury, K.E. Wareham, N. Riboli, E. Gunter, M. Brennan, P. Duell, E.J. Ferrari, P.
- Abstract
Recent evidence suggested a weak relationship between alcohol consumption and pancreatic cancer (PC) risk. In our study, the association between lifetime and baseline alcohol intakes and the risk of PC was evaluated, including the type of alcoholic beverages and potential interaction with smoking. Within the European Prospective Investigation into Cancer and Nutrition (EPIC) study, 1,283 incident PC (57% women) were diagnosed from 476,106 cancer-free participants, followed up for 14 years. Amounts of lifetime and baseline alcohol were estimated through lifestyle and dietary questionnaires, respectively. Cox proportional hazard models with age as primary time variable were used to estimate PC hazard ratios (HR) and their 95% confidence interval (CI). Alcohol intake was positively associated with PC risk in men. Associations were mainly driven by extreme alcohol levels, with HRs comparing heavy drinkers (>60 g/day) to the reference category (0.1–4.9 g/day) equal to 1.77 (95% CI: 1.06, 2.95) and 1.63 (95% CI: 1.16, 2.29) for lifetime and baseline alcohol, respectively. Baseline alcohol intakes from beer (>40 g/day) and spirits/liquors (>10 g/day) showed HRs equal to 1.58 (95% CI: 1.07, 2.34) and 1.41 (95% CI: 1.03, 1.94), respectively, compared to the reference category (0.1–2.9 g/day). In women, HR estimates did not reach statistically significance. The alcohol and PC risk association was not modified by smoking status. Findings from a large prospective study suggest that baseline and lifetime alcohol intakes were positively associated with PC risk, with more apparent risk estimates for beer and spirits/liquors than wine intake. © 2018 IARC/WHO
- Published
- 2018
9. IL-6 and CRP are superior in early severity stratification of acute pancreatitis
- Author
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Sternby, H., primary, Hartman, H., additional, Thorlacius, H., additional, and Regnér, S., additional
- Published
- 2019
- Full Text
- View/download PDF
10. Clinical features upon admission and outcomes of patients with acute pancreatitis – comparison between two European cohorts
- Author
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Sternby, H., primary, Regnér, S., additional, and de Madaria, E., additional
- Published
- 2018
- Full Text
- View/download PDF
11. Extrapancreatic necrosis is not uniformly identified by european radiologists - a prospective multicenter evaluation of the revised Atlanta classification
- Author
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Sternby, H., primary, Verdonk, R.C., additional, Aguilar, G., additional, Dimova, A., additional, Ignatavicius, P., additional, Ilzarbe, L., additional, Koiva, P., additional, Lantto, E., additional, Loigom, T., additional, Pentillä, A., additional, Regner, S., additional, Rosendahl, J., additional, Strahinova, V., additional, Zackrisson, S., additional, Zviniene, K., additional, and Bollen, T.L., additional
- Published
- 2016
- Full Text
- View/download PDF
12. Preset cut-off levels for predictive biomarkers in severe acute pancreatitis – Have we reached that far?
- Author
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Sternby, H., primary, Hartman, H., additional, Johansen, D., additional, Thorlacius, H., additional, and Regner, S., additional
- Published
- 2016
- Full Text
- View/download PDF
13. Prediction of mild disease in acute pancreatitis using routine and non-routine biomarkers
- Author
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Sternby, H., primary, Hartman, H., additional, Johansen, D., additional, Thorlacius, H., additional, and Regnér, S., additional
- Published
- 2016
- Full Text
- View/download PDF
14. Fatty liver disease and pancreatic inflammation-A lethal combination?
- Author
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Regnér S, Önnerhag K, and Sternby H
- Subjects
- Humans, Inflammation, Non-alcoholic Fatty Liver Disease diagnosis, Pancreatitis diagnosis, Pancreatitis etiology
- Published
- 2023
- Full Text
- View/download PDF
15. Pleuropulmonary pathologies in the early phase of acute pancreatitis correlate with disease severity.
- Author
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Luiken I, Eisenmann S, Garbe J, Sternby H, Verdonk RC, Dimova A, Ignatavicius P, Ilzarbe L, Koiva P, Penttilä AK, Regnér S, Dober J, Wohlgemuth WA, Brill R, Michl P, Rosendahl J, and Damm M
- Subjects
- Adult, Aged, Cohort Studies, Comorbidity, Disease Progression, Europe epidemiology, Female, Humans, Lung Diseases etiology, Lung Diseases pathology, Male, Middle Aged, Mortality, Pancreatitis complications, Pancreatitis pathology, Patient Acuity, Pleural Diseases diagnosis, Pleural Diseases etiology, Pleural Diseases pathology, Prevalence, Prognosis, Respiratory Insufficiency diagnosis, Respiratory Insufficiency epidemiology, Respiratory Insufficiency etiology, Retrospective Studies, Survival Analysis, Tomography, X-Ray Computed, Lung Diseases epidemiology, Pancreatitis diagnosis, Pancreatitis epidemiology, Pleural Diseases epidemiology
- Abstract
Background: Respiratory failure worsens the outcome of acute pancreatitis (AP) and underlying factors might be early detectable., Aims: To evaluate the prevalence and prognostic relevance of early pleuropulmonary pathologies and pre-existing chronic lung diseases (CLD) in AP patients., Methods: Multicentre retrospective cohort study. Caudal sections of the thorax derived from abdominal contrast enhanced computed tomography (CECT) performed in the early phase of AP were assessed. Independent predictors of severe AP were identified by binary logistic regression analysis. A one-year survival analysis using Kaplan-Meier curves and log rank test was performed., Results: 358 patients were analysed, finding pleuropulmonary pathologies in 81%. CECTs were performed with a median of 2 days (IQR 1-3) after admission. Multivariable analysis identified moderate to severe or bilateral pleural effusions (PEs) (OR = 4.16, 95%CI 2.05-8.45, p<0.001) and pre-existing CLD (OR = 2.93, 95%CI 1.17-7.32, p = 0.022) as independent predictors of severe AP. Log rank test showed a significantly worse one-year survival in patients with bilateral compared to unilateral PEs in a subgroup., Conclusions: Increasing awareness of the prognostic impact of large and bilateral PEs and pre-existing CLD could facilitate the identification of patients at high risk for severe AP in the early phase and thus improve their prognosis., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2022
- Full Text
- View/download PDF
16. Heparin-binding protein is significantly increased in acute pancreatitis.
- Author
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Sjöbeck M, Sternby H, Herwald H, Thorlacius H, and Regnér S
- Subjects
- Acute Disease, Antimicrobial Cationic Peptides, Blood Proteins, Carrier Proteins, Humans, Pancreatitis
- Abstract
Background: Most patients with acute pancreatitis (AP) experience mild, self-limiting disease with little or no need for hospital care. However, 20-25% of patients develop a more severe and potentially life-threatening condition with progressive systemic inflammatory response syndrome (SIRS) and multiorgan failure, resulting in high morbidity and mortality rates. Predicting disease severity at an early stage is important, as immediate supportive care has been demonstrated to reduce the incidence of SIRS and organ failure, improving patient outcome. Several studies have demonstrated elevated levels of heparin-binding protein (HBP) in patients with sepsis and septic shock, and HBP is believed to play a part in endothelial dysfunction leading to vascular leakage. As HBP levels increase prior to other known biomarkers, HBP has emerged as a promising early predictor of severe sepsis with organ dysfunction., Methods: Patients admitted to Skåne University Hospital in Malmö between 2010 and 2013 fulfilling the criteria for AP were identified in the emergency department and prospectively enrolled in this study. The primary outcome was measured levels of HBP upon hospital admission in patients with confirmed AP. Correlations among HBP concentrations, disease severity and fluid balance were considered secondary endpoints. The correlation between HBP levels and fluid balance were analysed using Pearson correlation, and the ability of HBP to predict moderately severe/severe AP was assessed using a receiver operating characteristic (ROC) curve., Results: The overall median HBP level in this study was 529 (307-898) ng/ml. There were no significant group differences in HBP levels based on AP severity. Fluid balance differed significantly between patients with mild versus moderately severe and severe pancreatitis, but we found no correlation between HBP concentration and fluid balance., Conclusions: HBP levels are dramatically increased in patients with AP, and these levels far exceed those previously reported in other conditions. In this study, we did not observe any significant correlation between HBP levels and disease severity or the need for intravenous fluid. Additional studies on HBP are needed to further explore the role of HBP in the pathogenesis of AP and its possible clinical implications., (© 2021. The Author(s).)
- Published
- 2021
- Full Text
- View/download PDF
17. The Initial Course of IL1β, IL-6, IL-8, IL-10, IL-12, IFN-γ and TNF-α with Regard to Severity Grade in Acute Pancreatitis.
- Author
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Sternby H, Hartman H, Thorlacius H, and Regnér S
- Subjects
- Adult, Aged, Aged, 80 and over, Biomarkers blood, Female, Humans, Male, Middle Aged, Pancreatitis pathology, Interferon-gamma blood, Interleukins blood, Pancreatitis blood, Tumor Necrosis Factor-alpha blood
- Abstract
Clinical reports on early immune dysregulation in acute pancreatitis (AP) are scarce. Herein we investigate the initial temporal development of selected biomarkers. Blood samples were taken at 0-24 and 25-48 h after onsets of AP were acquired. Mean values and temporal intermediate difference (delta-values) of IL-1β, IL-6, IL-8, IL-10, IL-12, IFN-γ and TNF-α were calculated. Differences between severity groups, predictive capacity of the biomarkers and association with severe disease were analyzed. Paired comparison of samples (n = 115) taken at 0-24 and 25-48 h after onsets of AP showed a change over time for IL-1β, IL-6, IL-8 and IL-10 ( p < 0.05) and a significant difference between severity groups after 24 h. In ROC-analysis an IL-6 cut-off level of 196.6 pg/mL could differentiate severe AP (sensitivity 81.9, specificity 91.3). The delta-values of IL-1β and IL-6 were significantly associated with severe outcomes (odds ratios 1.085 and 1.002, respectively). Data of this work demonstrate a distinct change in IL-1β, IL-8, IL-10 and IL-6 over the first 48 h after onset of AP. The temporal development of biomarkers can assist in the early stratification of the disease. Herein IL-1β and IL-6 were associated with severe disease, however the prognostic capacity of investigated biomarkers is low.
- Published
- 2021
- Full Text
- View/download PDF
18. Mean muscle attenuation correlates with severe acute pancreatitis unlike visceral adipose tissue and subcutaneous adipose tissue.
- Author
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Sternby H, Mahle M, Linder N, Erichson-Kirst L, Verdonk RC, Dimova A, Ignatavicius P, Ilzarbe L, Koiva P, Penttilä A, Regnér S, Bollen TL, Brill R, Stangl F, Wohlgemuth WA, Singh V, Busse H, Michl P, Beer S, and Rosendahl J
- Subjects
- Adult, Aged, Body Composition, Female, Humans, Male, Middle Aged, Odds Ratio, ROC Curve, Radiographic Image Enhancement, Severity of Illness Index, Tomography, X-Ray Computed methods, Intra-Abdominal Fat diagnostic imaging, Intra-Abdominal Fat pathology, Muscles diagnostic imaging, Muscles pathology, Pancreatitis diagnostic imaging, Pancreatitis pathology, Subcutaneous Fat diagnostic imaging, Subcutaneous Fat pathology
- Abstract
Background: Acute pancreatitis (AP) is a frequent disorder with considerable morbidity and mortality. Obesity has previously been reported to influence disease severity., Objective: The aim of this study was to investigate the association of adipose and muscle parameters with the severity grade of AP., Methods: In total 454 patients were recruited. The first contrast-enhanced computed tomography of each patient was reviewed for adipose and muscle tissue parameters at L3 level. Associations with disease severity were analysed through logistic regression analysis. The predictive capacity of the parameters was investigated using receiver operating characteristic (ROC) curves., Results: No distinct variation was found between the AP severity groups in either adipose tissue parameters (visceral adipose tissue and subcutaneous adipose tissue) or visceral muscle ratio. However, muscle mass and mean muscle attenuation differed significantly with p -values of 0.037 and 0.003 respectively. In multivariate analysis, low muscle attenuation was associated with severe AP with an odds ratio of 4.09 (95% confidence intervals: 1.61-10.36, p -value 0.003). No body parameter presented sufficient predictive capability in ROC-curve analysis., Conclusions: Our results demonstrate that a low muscle attenuation level is associated with an increased risk of severe AP. Future prospective studies will help identify the underlying mechanisms and characterise the influence of body composition parameters on AP., (© Author(s) 2019.)
- Published
- 2019
- Full Text
- View/download PDF
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