462 results on '"Evans AE"'
Search Results
2. The Migraine-Anxiety Comorbidity Among Migraineurs: A Systematic Review
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Karimi, L, Wijeratne, T, Crewther, SG, Evans, AE, Ebaid, D, Khalil, H, Karimi, L, Wijeratne, T, Crewther, SG, Evans, AE, Ebaid, D, and Khalil, H
- Abstract
Background: Migraine is recognized as a neurological condition that is often associated with comorbid psychiatric symptoms such as anxiety, depression, bipolar disorder and/or panic disorder. Though some studies have demonstrated the link between migraine and anxiety disorders, there are no systematic reviews that have been published in this area to summarize the evidence. The aim of the present study is to systematically review the literature associated with comorbidity of migraine and anxiety disorders among migraineurs compared to non-migraineurs. Methods: The present systematic review included population-based, cohort and cross-sectional studies if they were reporting the frequency of migraine with either anxiety or depression as diagnosed by a medical practitioner according to the International Classification of Headache Disorders (ICHD-2/3). Results: Eight eligible studies from 2060 relevant citations were included in the review. All participants were migraine patients from both primary care and outpatient settings, as well as tertiary headache and anxiety centers, and were compared to non-migraineurs. The results of the systematic review showed that there is a strong and consistent relationship between migraine and anxiety. The co-morbidity of co-occurrence for migraine and anxiety has an average OR of 2.33 (2.20-2.47) among the prevalence and cross sectional studies and an average RR of 1.63 (1.37-1.93) for two cohort studies; The major limitations of included studies were small sample sizes and a lack of adjusting of confounding factors. Conclusion: The results highlight the need for inclusion of an anxiety screening tool during initial assessments of migraine patients by medical practitioners and/or physicians and may explain why some anxiolytic medications work better than others for migraine mitigation.
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- 2021
3. The Prevalence of Migraine With Anxiety Among Genders
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Karimi, L, Crewther, SG, Wijeratne, T, Evans, AE, Afshari, L, Khalil, H, Karimi, L, Crewther, SG, Wijeratne, T, Evans, AE, Afshari, L, and Khalil, H
- Abstract
Objective: The aims of the present systematic review were to explore the prevalence of migraine with anxiety exclusively and determine if and why there are likely to be differences across genders. Introduction: Migraine is a very common neurological disorder and cause of productive disability worldwide that is more frequent in women of childbearing age than males. Previous studies have frequently demonstrated comorbidity of migraine and other psychiatric disorders. Although the prevalence of migraine across gender is well-established there are few if any systematic reviews on the prevalence of migraine comorbidity with anxiety cross-genders. Methods: The present systematic review included prevalence studies, clinic-based and cohort studies that reported the frequency of migraine with anxiety within the study sample. Eleven studies were included in the review after screening by two independent reviewers. Studies included participants who were 16 years and older diagnosed with migraine. Results: The main findings of this review indicated that anxiety is a major comorbidity of migraine worldwide, with a wide range (16-83%) of prevalence and a mean of ~43% of patients experiencing comorbid symptoms. Subjective anxiety symptoms appear to be greater among males with migraine than females which could be attributable to both environmental and/or hormonal and genetic predispositions. Conclusions: The results reemphasize the high prevalence of migraine and comorbid anxiety symptoms worldwide while showing that although migraine is far more prevalent among women in general co-morbidity of migraine with anxiety unfolds a different gender difference. The results highlight the significance of exploring the impact of existing and pre-existing comorbid conditions of patients with migraines and further consideration into their diagnostic and treatment strategies.
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- 2020
4. Pre-hospital coronary care and coronary fatality in the Belfast and Glasgow MONICA populations
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Moore, W, Kee, F, Evans, AE, McCrum-Gardner, EE, Morrison, C, and Tunstall-Pedoe, H
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- 2005
5. Psychosocial risk factors for heart disease in France and Northern Ireland: The Prospective Epidemiological Study of Myocardial Infarction (PRIME)
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Sykes, DH, Arveiler, D, Salters, CP, Ferrieres, J, McCrum, E, Amouyel, P, Bingham, A, Montaye, M, Ruidavets, J-B, Haas, B, Ducimetiere, P, and Evans, AE
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- 2002
6. 1678 Historical perspectives on occupational health in ireland
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D Blanc, Paul, primary, Menendez-Navarro, Alfredo, additional, Hayes, J, additional, Evans, AE, additional, Addley, K, additional, and Malone, JM, additional
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- 2018
- Full Text
- View/download PDF
7. 1678b Flax and linen in the history of irish industrial health
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Evans, AE, primary
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- 2018
- Full Text
- View/download PDF
8. Collaborative meta-analysis of prospective studies of plasma fibrinogen and cardiovascular disease
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Kostis, JB, Wilson, AC, Folsom, AR, Chambless, L, Wu, K, Benderly, M, Goldbourt, U, Willeit, J, Kiechl, S, Yarnell, JWG, Sweetnam, PM, Elwood, PC, Cushman, M, Psaty, BM, Tybjaerg-Hansen, A, Haverkate, F, de Maat, MPM, Thompson, SG, Fowkes, FGR, Lee, AJ, Smith, FB, Salomaa, V, Rasi, V, Vahtera, E, Jousilahti, P, Pekkanen, J, D'Agostino, R, Kannel, WB, Levy, D, Wilson, PWF, Arocha-Pinango, CL, Rodriguez-Larralde, A, Nagy, E, Mijares, M, Espinosa, R, Roa, E, Ryder, E, Diez-Ewald, MP, Campos, G, Fernandez, V, Torres, E, Marchioli, R, Valagussa, F, Rosengren, A, Wilhelmsen, L, Lappas, G, Eriksson, H, Cremer, P, Nagel, D, Curb, JD, Rodriguez, B, Yano, K, Salonen, JT, Nyyssonen, K, Tuomainen, TP, Hedblad, B, Lind, P, Loewel, H, Hense, HW, Koenig, W, Meade, TW, Cooper, JA, De Stavola, B, Garrow, K, Knottenbelt, C, Miller, GJ, Bauer, KA, Rosenberg, RD, Sato, S, Kitamura, A, Naito, Y, Iso, H, Palosuo, T, Ducimetiere, P, Amouyel, P, Arveiler, D, Evans, AE, Ferrieres, J, Juhan-Vague, I, Schulte, H, Assmann, G, Cantin, B, Lamarche, B, Despres, JP, Dagenais, GR, Tunstall-Pedoe, H, Lowe, GDO, Collins, R, Danesh, J, Dickinson, A, Lewington, S, Memon, A, Thompson, S, Walker, M, Wheeler, J, Ben-Shlomo, Y, Smith, GD, Palmieri, V, Yeh, JL, Rudnicka, A, Brennan, P, Cooper, J, Rodeghiero, F, Tosetto, A, Shepherd, J, Ford, I, Norrie, J, Brunner, E, Shipley, M, Feskens, EJM, Kromhout, D, and Collaboration, FS
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medicine.medical_specialty ,Epidemiology ,business.industry ,Regression dilution ,Confounding ,Fibrinogen ,Regression analysis ,Fibrinogen Measurement ,Surgery ,Meta-Analysis as Topic ,Cardiovascular Diseases ,Internal medicine ,Meta-analysis ,Data Interpretation, Statistical ,Medicine ,Humans ,Prospective Studies ,Risk factor ,Cooperative Behavior ,Cardiology and Cardiovascular Medicine ,business ,Prospective cohort study ,Biomarkers ,medicine.drug - Abstract
BACKGROUND: Many long-term studies have reported on associations of plasma fibrinogen concentration with cardiovascular disease, but few have been large enough to provide reliable estimates in different circumstances. Moreover, most published prospective studies have related disease risk only to baseline values of plasma fibrinogen (which can lead to substantial underestimation of any risk relationships) and have corrected only for baseline values of possible confounding factors (which can lead to residual biases). OBJECTIVES: By appropriate combination of data from individual participants from all relevant prospective studies in a systematic 'meta-analysis', with correction for regression dilution, the Fibrinogen Studies Collaboration will aim to characterize more precisely than has previously been possible the strength and shape of the age- and sex-specific associations of plasma fibrinogen with coronary heart disease (and, where data are sufficient, with other vascular diseases). It will also help to determine to what extent such associations are independent of possible confounding factors. METHODS: A central database has been established containing data on plasma fibrinogen, sex and other potential confounding factors, age at baseline fibrinogen measurement, age at event or at last follow-up, major vascular morbidity and cause-specific mortality. Information about any repeat measurements of fibrinogen and potential confounding factors is being sought to allow study-specific correction for regression dilution. The analyses will involve age-specific regression models. Synthesis of the available prospective studies of plasma fibrinogen will yield information on more than 10000 incident cardiovascular deaths and events among the approximately 200000 total participants who have been monitored, on average, for about 10 years.
- Published
- 2016
9. Plasma fibrinogen level and the risk of major cardiovascular diseases and nonvascular mortality : an individual participant Metaanalysis
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Danesh, J, Lewington, S, Thompson, SG, Lowe, GD, Collins, R, Kostis, JB, Wilson, AC, Folsom, AR, Wu, K, Benderly, M, Goldbourt, U, Willeit, J, Kiechl, S, Yarnell, JW, Sweetnam, PM, Elwood, PC, Cushman, M, Psaty, BM, Tracy, RP, Tybjaerg-Hansen, A, Haverkate, F, de Maat, MP, Fowkes, FG, Lee, AJ, Smith, FB, Salomaa, V, Harald, K, Rasi, R, Vahtera, E, Jousilahti, P, Pekkanen, J, D'Agostino, R, Kannel, WB, Wilson, PW, Tofler, G, Arocha-Piñango, CL, Rodriguez-Larralde, A, Nagy, E, Mijares, M, Espinosa, R, Rodriquez-Roa, E, Ryder, E, Diez-Ewald, MP, Campos, G, Fernandez, V, Torres, E, Marchioli, R, Valagussa, F, Rosengren, A, Wilhelmsen, L, Lappas, G, Eriksson, H, Cremer, P, Nagel, D, Curb, JD, Rodriguez, B, Yano, K, Salonen, JT, Nyyssönen, K, Tuomainen, TP, Hedblad, B, Lind, P, Loewel, H, Koenig, W, Meade, TW, Cooper, JA, De Stavola, B, Knottenbelt, C, Miller, GJ, Bauer, KA, Rosenberg, RD, Sato, S, Kitamura, A, Naito, Y, Palosuo, T, Ducimetiere, P, Amouyel, P, Arveiler, D, Evans, AE, Ferrieres, J, Juhan-Vague, I, Bingham, A, Schulte, H, Assmann, G, Cantin, B, Lamarche, B, Després, JP, Dagenais, GR, Tunstall-Pedoe, H, Woodward, M, Ben-Shlomo, Y, Davey Smith, G, Palmieri, V, Yeh, JL, Rudnicka, A, Ridker, P, Rodeghiero, F, Tosetto, A, Shepherd, J, Ford, I, Robertson, M, Brunner, E, Shipley, M, Feskens, EJ, Kromhout, D, Dickinson, A, Ireland, B, Juzwishin, K, Kaptoge, S, Memon, A, Sarwar, N, Walker, M, Wheeler, J, White, I, and Wood, A
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Adult ,Risk ,medicine.medical_specialty ,base-line findings ,blood-viscosity ,Nutrition and Disease ,Regression dilution ,Blood viscosity ,Myocardial Infarction ,Context (language use) ,Coronary Disease ,c-reactive protein ,edinburgh artery ,Internal medicine ,Cause of Death ,Voeding en Ziekte ,medicine ,follow-up ,Humans ,Vascular Diseases ,Stroke ,Aged ,Proportional Hazards Models ,VLAG ,hemostatic factors ,business.industry ,Proportional hazards model ,Confounding ,Hazard ratio ,Fibrinogen ,General Medicine ,Middle Aged ,medicine.disease ,myocardial-infarction ,Surgery ,relative risk ,Relative risk ,factor-vii ,business ,coronary-heart-disease - Abstract
CONTEXT: Plasma fibrinogen levels may be associated with the risk of coronary heart disease (CHD) and stroke. OBJECTIVE: To assess the relationships of fibrinogen levels with risk of major vascular and with risk of nonvascular outcomes based on individual participant data. DATA SOURCES: Relevant studies were identified by computer-assisted searches, hand searches of reference lists, and personal communication with relevant investigators. STUDY SELECTION: All identified prospective studies were included with information available on baseline fibrinogen levels and details of subsequent major vascular morbidity and/or cause-specific mortality during at least 1 year of follow-up. Studies were excluded if they recruited participants on the basis of having had a previous history of cardiovascular disease; participants with known preexisting CHD or stroke were excluded. DATA EXTRACTION: Individual records were provided on each of 154,211 participants in 31 prospective studies. During 1.38 million person-years of follow-up, there were 6944 first nonfatal myocardial infarctions or stroke events and 13,210 deaths. Cause-specific mortality was generally available. Analyses involved proportional hazards modeling with adjustment for confounding by known cardiovascular risk factors and for regression dilution bias. DATA SYNTHESIS: Within each age group considered (40-59, 60-69, and > or =70 years), there was an approximately log-linear association with usual fibrinogen level for the risk of any CHD, any stroke, other vascular (eg, non-CHD, nonstroke) mortality, and nonvascular mortality. There was no evidence of a threshold within the range of usual fibrinogen level studied at any age. The age- and sex- adjusted hazard ratio per 1-g/L increase in usual fibrinogen level for CHD was 2.42 (95% confidence interval [CI], 2.24-2.60); stroke, 2.06 (95% CI, 1.83-2.33); other vascular mortality, 2.76 (95% CI, 2.28-3.35); and nonvascular mortality, 2.03 (95% CI, 1.90-2.18). The hazard ratios for CHD and stroke were reduced to about 1.8 after further adjustment for measured values of several established vascular risk factors. In a subset of 7011 participants with available C-reactive protein values, the findings for CHD were essentially unchanged following additional adjustment for C-reactive protein. The associations of fibrinogen level with CHD or stroke did not differ substantially according to sex, smoking, blood pressure, blood lipid levels, or several features of study design. CONCLUSIONS: In this large individual participant meta-analysis, moderately strong associations were found between usual plasma fibrinogen level and the risks of CHD, stroke, other vascular mortality, and nonvascular mortality in a wide range of circumstances in healthy middle-aged adults. Assessment of any causal relevance of elevated fibrinogen levels to disease requires additional research.
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- 2005
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- View/download PDF
10. Systematically missing confounders in individual participant data meta-analysis of observational cohort studies
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Fibrinogen Studies Collaboration, Jackson, D, White, I, Kostis, JB, Wilson, AC, Folsom, AR, Wu, K, Chambless, L, Benderly, M, Goldbourt, U, Willeit, J, Kiechl, S, Yarnell, JW, Sweetnam, PM, Elwood, PC, Cushman, M, Psaty, BM, Tracy, RP, Tybjaerg-Hansen, A, Haverkate, F, de Maat, MP, Thompson, SG, Fowkes, FG, Lee, AJ, Smith, FB, Salomaa, V, Harald, K, Rasi, V, Vahtera, E, Jousilahti, P, D'Agostino, R, Kannel, WB, Wilson, PW, Tofler, G, Levy, D, Marchioli, R, Valagussa, F, Rosengren, A, Wilhelmsen, L, Lappas, G, Eriksson, H, Cremer, P, Nagel, D, Curb, JD, Rodriguez, B, Yano, K, Salonen, J, Nyyssönen, K, Tuomainen, TP, Hedblad, B, Engström, G, Berglund, G, Loewel, H, Koenig, W, Hense, HW, Meade, TW, Cooper, JA, De Stavola, B, Knottenbelt, C, Miller, GJ, Bauer, KA, Rosenberg, RD, Sato, S, Kitamura, A, Naito, Y, Iso, H, Palosuo, T, Ducimetiere, P, Amouyel, P, Arveiler, D, Evans, AE, Ferrieres, J, Juhan-Vague, I, Bingham, A, Schulte, H, Assmann, G, Cantin, B, Lamarche, B, Despres, JP, Dagenais, GR, Tunstall-Pedoe, H, Lowe, GD, Woodward, M, Ben-Shlomo, Y, Davey Smith, G, Palmieri, V, Yeh, JL, Rudnicka, A, Brennan, P, Ridker, P, Rodeghiero, F, Tosetto, A, Shepherd, J, Ford, I, Robertson, M, Brunner, E, Shipley, M, Feskens, EJ, Di Angelantonio, E, Kaptoge, S, Lewington, S, Sarwar, N, Walker, M, Watson, S, White, IR, Wood, AM, and Danesh, J
- Abstract
One difficulty in performing meta-analyses of observational cohort studies is that the availability of confounders may vary between cohorts, so that some cohorts provide fully adjusted analyses while others only provide partially adjusted analyses. Commonly, analyses of the association between an exposure and disease either are restricted to cohorts with full confounder information, or use all cohorts but do not fully adjust for confounding. We propose using a bivariate random-effects meta-analysis model to use information from all available cohorts while still adjusting for all the potential confounders. Our method uses both the fully adjusted and the partially adjusted estimated effects in the cohorts with full confounder information, together with an estimate of their within-cohort correlation. The method is applied to estimate the association between fibrinogen level and coronary heart disease incidence using data from 154,012 participants in 31 cohorts
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- 2009
11. Systematically missing confounders in individual participant data meta-analysis of observational cohort studies
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Jackson, D, White, I, Kostis, JB, Wilson, AC, Folsom, AR, Wu, K, Chambless, L, Benderly, M, Goldbourt, U, Willeit, J, Kiechl, S, Yarnell, JW, Sweetnam, PM, Elwood, PC, Cushman, M, Psaty, BM, Tracy, RP, Tybjaerg-Hansen, A, Haverkate, F, de Maat, MP, Thompson, SG, Fowkes, FG, Lee, AJ, Smith, FB, Salomaa, V, Harald, K, Rasi, V, Vahtera, E, Jousilahti, P, D'Agostino, R, Kannel, WB, Wilson, PW, Tofler, G, Levy, D, Marchioli, R, Valagussa, F, Rosengren, A, Wilhelmsen, L, Lappas, G, Eriksson, H, Cremer, P, Nagel, D, Curb, JD, Rodriguez, B, Yano, K, Salonen, J, Nyyssönen, K, Tuomainen, TP, Hedblad, B, Engström, G, Berglund, G, Loewel, H, Koenig, W, Hense, HW, Meade, TW, Cooper, JA, De Stavola, B, Knottenbelt, C, Miller, GJ, Bauer, KA, Rosenberg, RD, Sato, S, Kitamura, A, Naito, Y, Iso, H, Palosuo, T, Ducimetiere, P, Amouyel, P, Arveiler, D, Evans, AE, Ferrieres, J, Juhan-Vague, I, Bingham, A, Schulte, H, Assmann, G, Cantin, B, Lamarche, B, Despres, JP, Dagenais, GR, Tunstall-Pedoe, H, Lowe, GD, Woodward, M, Ben-Shlomo, Y, Davey Smith, G, Palmieri, V, Yeh, JL, Rudnicka, A, Brennan, P, Ridker, P, Rodeghiero, F, Tosetto, A, Shepherd, J, Ford, I, Robertson, M, Brunner, E, Shipley, M, Feskens, EJ, Di Angelantonio, E, Kaptoge, S, Lewington, S, Sarwar, N, Walker, M, Watson, S, White, IR, Wood, AM, and Danesh, J
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Statistics and Probability ,Male ,Nutrition and Disease ,Epidemiology ,Coronary Disease ,Bivariate analysis ,Logistic regression ,01 natural sciences ,survival analysis ,Cohort Studies ,010104 statistics & probability ,03 medical and health sciences ,0302 clinical medicine ,Meta-Analysis as Topic ,Voeding en Ziekte ,Statistics ,Medicine ,Humans ,Computer Simulation ,030212 general & internal medicine ,0101 mathematics ,observational studies ,patient data ,Survival analysis ,time ,VLAG ,Models, Statistical ,aggregate data ,model ,business.industry ,Incidence (epidemiology) ,Confounding ,Fibrinogen ,confounders ,event outcomes ,meta-analysis ,Meta-analysis ,Data Interpretation, Statistical ,missing covariates ,logistic-regression analysis ,Observational study ,Female ,heterogeneity ,business ,Demography ,Cohort study ,Research Article - Abstract
One difficulty in performing meta-analyses of observational cohort studies is that the availability of confounders may vary between cohorts, so that some cohorts provide fully adjusted analyses while others only provide partially adjusted analyses. Commonly, analyses of the association between an exposure and disease either are restricted to cohorts with full confounder information, or use all cohorts but do not fully adjust for confounding. We propose using a bivariate random-effects meta-analysis model to use information from all available cohorts while still adjusting for all the potential confounders. Our method uses both the fully adjusted and the partially adjusted estimated effects in the cohorts with full confounder information, together with an estimate of their within-cohort correlation. The method is applied to estimate the association between fibrinogen level and coronary heart disease incidence using data from 154 012 participants in 31 cohorts.† Copyright © 2009 John Wiley & Sons, Ltd.
- Published
- 2009
12. Dose-dependent effects of folic acid on blood concentrations of homocysteine: a meta-analysis of the randomized trials
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Clarke, R, Frost, C, Sherliker, P, Lewington, S, Collins, R, Brattstrom, L, Brouwer, I, van Dusseldorp, M, Steegers-Theunissen, RPM, Cuskelly, G, Ward, M, McNulty, H, Scott, J, den Heijer, M, Blom, H, van der Put, N, Shorah, CJ, Malinow, MR, McMahon, M, Tobert, J, Kush, D, Joosten, E, Riezier, R, Pietrzik, K, Dierkes, J, Bronstrup, A, Jacques, P, Mason, J, Rosenberg, I, Thambyrajah, J, Landray, M, Townend, J, Wheeler, D, Ubbink, J, van Oort, F, Melse-Boonstra, A, Verhoef, P, Woodside, JV, Yarnell, J, Young, IS, Evans, AE, Wald, D, Law, M, Wald, N, and Homocysteine, LTC
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- 2005
13. Plasma fibrinogen level and the risk of major cardiovascular diseases and nonvascular mortality: an individual participant meta-analysis
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Fibrinogen Studies Collaboration, Danesh, John, Lewington, Sarah, Thompson, Simon G, Lowe, Gordon DO, Collins, Rory, Kostis, JB, Wilson, AC, Folsom, AR, Wu, K, Benderly, M, Goldbourt, U, Willeit, J, Kiechl, S, Yarnell, JWG, Sweetnam, PM, Elwood, PC, Cushman, M, Psaty, BM, Tracy, RP, Tybjaerg-Hansen, A, Haverkate, F, de Maat, MPM, Fowkes, FGR, Lee, AJ, Smith, FB, Salomaa, V, Harald, K, Rasi, R, Vahtera, E, Jousilahti, P, Pekkanen, J, D'Agostino, R, Kannel, WB, Wilson, PWF, Tofler, G, Arocha-Piñango, CL, Rodriguez-Larralde, A, Nagy, E, Mijares, M, Espinosa, R, Rodriquez-Roa, E, Ryder, E, Diez-Ewald, MP, Campos, G, Fernandez, V, Torres, E, Marchioli, R, Valagussa, F, Rosengren, A, Wilhelmsen, L, Lappas, G, Eriksson, H, Cremer, P, Nagel, D, Curb, JD, Rodriguez, B, Yano, K, Salonen, JT, Nyyssönen, K, Tuomainen, T-P, Hedblad, B, Lind, P, Loewel, H, Koenig, W, Meade, TW, Cooper, JA, De Stavola, B, Knottenbelt, C, Miller, GJ, Bauer, KA, Rosenberg, RD, Sato, S, Kitamura, A, Naito, Y, Palosuo, T, Ducimetiere, P, Amouyel, P, Arveiler, D, Evans, AE, Ferrieres, J, Juhan-Vague, I, Bingham, A, Schulte, H, Assmann, G, Cantin, B, Lamarche, B, Després, J-P, Dagenais, GR, Tunstall-Pedoe, H, Woodward, M, Ben-Shlomo, Y, Davey Smith, G, Palmieri, V, Yeh, JL, Rudnicka, A, Ridker, P, Rodeghiero, F, Tosetto, A, Shepherd, J, Ford, I, Robertson, M, Brunner, E, Shipley, M, Feskens, EJM, Kromhout, D, Dickinson, A, Ireland, B, Juzwishin, K, Kaptoge, S, Lewington, S, Memon, A, Sarwar, N, Walker, M, Wheeler, J, White, I, and Wood, A
- Abstract
CONTEXT: Plasma fibrinogen levels may be associated with the risk of coronary heart disease (CHD) and stroke. OBJECTIVE: To assess the relationships of fibrinogen levels with risk of major vascular and with risk of nonvascular outcomes based on individual participant data. DATA SOURCES: Relevant studies were identified by computer-assisted searches, hand searches of reference lists, and personal communication with relevant investigators. STUDY SELECTION: All identified prospective studies were included with information available on baseline fibrinogen levels and details of subsequent major vascular morbidity and/or cause-specific mortality during at least 1 year of follow-up. Studies were excluded if they recruited participants on the basis of having had a previous history of cardiovascular disease; participants with known preexisting CHD or stroke were excluded. DATA EXTRACTION: Individual records were provided on each of 154,211 participants in 31 prospective studies. During 1.38 million person-years of follow-up, there were 6944 first nonfatal myocardial infarctions or stroke events and 13,210 deaths. Cause-specific mortality was generally available. Analyses involved proportional hazards modeling with adjustment for confounding by known cardiovascular risk factors and for regression dilution bias. DATA SYNTHESIS: Within each age group considered (40-59, 60-69, and > or =70 years), there was an approximately log-linear association with usual fibrinogen level for the risk of any CHD, any stroke, other vascular (eg, non-CHD, nonstroke) mortality, and nonvascular mortality. There was no evidence of a threshold within the range of usual fibrinogen level studied at any age. The age- and sex- adjusted hazard ratio per 1-g/L increase in usual fibrinogen level for CHD was 2.42 (95% confidence interval [CI], 2.24-2.60); stroke, 2.06 (95% CI, 1.83-2.33); other vascular mortality, 2.76 (95% CI, 2.28-3.35); and nonvascular mortality, 2.03 (95% CI, 1.90-2.18). The hazard ratios for CHD and stroke were reduced to about 1.8 after further adjustment for measured values of several established vascular risk factors. In a subset of 7011 participants with available C-reactive protein values, the findings for CHD were essentially unchanged following additional adjustment for C-reactive protein. The associations of fibrinogen level with CHD or stroke did not differ substantially according to sex, smoking, blood pressure, blood lipid levels, or several features of study design. CONCLUSIONS: In this large individual participant meta-analysis, moderately strong associations were found between usual plasma fibrinogen level and the risks of CHD, stroke, other vascular mortality, and nonvascular mortality in a wide range of circumstances in healthy middle-aged adults. Assessment of any causal relevance of elevated fibrinogen levels to disease requires additional research.
- Published
- 2005
14. NERVE GROWTH-FACTOR RECEPTOR EXPRESSION IN PERIPHERAL AND CENTRAL NEUROECTODERMAL TUMORS, OTHER PEDIATRIC BRAIN-TUMORS, AND DURING DEVELOPMENT OF THE ADRENAL-GLAND
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BAKER, DL, Molenaar, Ineke, TROJANOWSKI, JQ, EVANS, AE, ROSS, AH, RORKE, LB, PACKER, RJ, LEE, VMY, and PLEASURE, D
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HIGH-AFFINITY ,NGF RECEPTOR ,SOFT-TISSUE TUMORS ,MEDULLOBLASTOMA CELL-LINE ,HUMAN NEURO-BLASTOMA ,MONOCLONAL-ANTIBODIES ,HEALTH-ORGANIZATION CLASSIFICATION ,BINDING-SITES ,IMMUNOHISTOCHEMICAL ANALYSIS ,FIBRILLARY ACIDIC PROTEIN - Abstract
Nerve growth factor (NGF) is important to the survival, development, and differentiation of neurons. Its action is mediated by a specific cell surface transmembrane glycoprotein, nerve growth factor receptor (NGFR). In this study, NGFR expression by human fetal and adult adrenal medullary tissue, peripheral nervous system (PNS) neuroectodermal tumors (neuroblastoma, ganglioneuroblastoma, ganglioneuroma), pediatric primitive neuroectodermal tumors (PNETs) of the central nervous system (CNS), and CNS gliomas was examined by an immunohistochemical technique. Sixty-nine tumors in total were probed in this manner. Nerve growth factor receptor immunoreactivity was confined to nerve fibers and clusters of primitive-appearing cells in the fetal adrenal, and to nerve fibers and ganglion cells of the adult adrenal medulla; adrenal chromaffin cells were negative. In PNS neuroectodermal tumors, there was NGFR expression in tumor cells of 6 of 11 neuroblastomas and 6 of 6 ganglioneuroblastomas or ganglioneuromas. Thirteen of thirty-five CNS PNETs showed NGFR positivity. In most CNS PNETs, NGFR was restricted to scattered single or small groups of cells, but two tumors with astroglial differentiation showed much more extensive immunoreactivity. Most astrocytomas (11 of 14) and all ependymomas (3 of 3) were intensely NGFR positive.
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- 1991
15. Prevalence and awareness of excess weight in 13 and 14 year olds in Northern Ireland using recent international guidelines
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Yarnell, JWG, primary, McCrum, EE, additional, Patterson, CC, additional, Skidmore, P, additional, Shields, MD, additional, McMahon, J, additional, and Evans, AE, additional
- Published
- 2001
- Full Text
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16. Serum copper and zinc in random samples of the population of Northern Ireland
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McMaster, D, primary, McCrum, E, additional, Patterson, CC, additional, Kerr, MM, additional, O'Reilly, D, additional, Evans, AE, additional, and Love, AH, additional
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- 1992
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17. The transcobalamin (TCN2) 776C<GT>G polymorphism affects homocysteine concentrations among subjects with low vitamin B(12) status.
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Stanislawska-Sachadyn A, Woodside JV, Sayers CM, Yarnell JW, Young IS, Evans AE, Mitchell LE, and Whitehead AS
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- 2010
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18. Cognitive and home environmental predictors of change in sugar-sweetened beverage consumption among adolescents.
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Ezendam NP, Evans AE, Stigler MH, Brug J, and Oenema A
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- 2010
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19. Preschooler feeding practices and beliefs: differences among Spanish- and English-speaking WIC clients.
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Seth JG, Evans AE, Harris KK, Loyo JJ, Ray TC, Spaulding C, and Gottlieb NH
- Abstract
This study explored preschooler feeding practices and beliefs among Spanish- and English-speaking WIC participants in Texas. The Preschooler Feeding Questionnaire examined 9 dimensions of the parent-child feeding interaction among 235 caregivers. Results from ANOVA and post hoc analyses demonstrated significant differences in reported preschooler feeding practices and beliefs among Spanish-speaking Hispanics in comparison with English-speaking Hispanics and non-Hispanics. No significant differences were found between English-speaking Hispanics and non-Hispanics. Results indicated that acculturation may impact behaviors apart from ethnicity. Nutrition professionals should understand and acknowledge the cultural context of the parent-child feeding interaction when developing programs. [ABSTRACT FROM AUTHOR]
- Published
- 2007
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20. Changing the home nutrition environment: effects of a nutrition and media literacy pilot intervention.
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Evans AE, Dave J, Tanner A, Duhe S, Condrasky M, Wilson D, Griffin S, Palmer M, Evans M, Evans, Alexandra E, Dave, Jayna, Tanner, Andrea, Duhe, Sonya, Condrasky, Margaret, Wilson, Dawn, Griffin, Sarah, Palmer, Meredith, and Evans, Martin
- Abstract
The specific aim for this pilot study was to evaluate the effectiveness of a nutrition and media literacy intervention targeting elementary students and their parents. The purpose of the intervention was to increase child fruit and vegetables (FV) consumption and change the home nutrition environment (measured with FV availability and accessibility and parental social support). During the intervention, students learned about nutrition, the role media plays in shaping values concerning nutrition, and developed a media campaign for their parents. A quasi-experimental research design was used to evaluate the effectiveness of the intervention. The media intervention was effective in changing the home environment. [ABSTRACT FROM AUTHOR]
- Published
- 2006
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21. Outcome expectations, barriers, and strategies for healthful eating: a perspective from adolescents from low-income families.
- Author
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Evans AE, Wilson DK, Buck J, Torbett H, Williams J, Evans, Alexandra E, Wilson, Dawn K, Buck, Jacquelynn, Torbett, Heather, and Williams, Joel
- Abstract
To better understand outcome expectations, barriers, and strategies for healthful eating, 5 structured focus groups were conducted with adolescents from low-income families (n = 48; 83% Black students; 10-14 years old). The focus group questions dealt with healthful eating in different settings: home, school, and other eating establishments. Results suggested that healthful eating is important to this population, but perceived barriers prevent the consistent consumption of healthful foods. Strategies suggested by participants to increase healthful eating (eg, parents and schools making healthy foods that look and taste good more available) should be considered when developing nutrition interventions for adolescents from low-income families. [ABSTRACT FROM AUTHOR]
- Published
- 2006
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22. Predicting adolescent risk behaviors based on an ecological framework and assets.
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Reininger BM, Evans AE, Griffin SF, Sanderson M, Vincent ML, Valois RF, and Parra-Medina D
- Abstract
OBJECTIVES: To examine the relationship between an aggregate risk score (smoking, drinking, and number of sex partners) and measures of youth assets in a sample of 3439 youth aged 14-18 years. METHODS: Linear regression models for African American and white males and females predicted an aggregate risk score. RESULTS: After adjustments, the youth asset most predictive of risk was self/peer values regarding risk behaviors. Perceived school support was also predictive. CONCLUSIONS: Taking an ecological approach to the measurement of adolescent health behaviors contributes to our understanding of these risk behaviors. [ABSTRACT FROM AUTHOR]
- Published
- 2005
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23. Research and professional briefs. Fruit and vegetable consumption among Mexican-American college students.
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Evans AE, Sawyer-Morse MK, and Betsinger A
- Published
- 2000
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24. Diet, lifestyle and health in Northern Ireland
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Evans, AE
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Book Review - Published
- 1990
25. Epidemiology of Helicobacter pylori infection among 4742 randomly selected subjects from Northern Ireland.
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Murray, LJ, McCrum, E, Evans, AE, Bamford, KB, Murray, L J, McCrum, E E, Evans, A E, and Bamford, K B
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AGE distribution ,ALCOHOL drinking ,HELICOBACTER diseases ,HELICOBACTER pylori ,STATISTICAL sampling ,SERODIAGNOSIS ,SEX distribution ,SMOKING ,SOCIAL classes ,STATURE ,SURVEYS ,BODY mass index ,DISEASE prevalence - Abstract
Background: Despite the widespread prevalence and serious clinical sequelae of infection with Helicobacter pylori, there have been few large population-based studies, using randomly selected subjects, examining the epidemiology of this infection.Aim: To examine the distribution and determinants of H. pylori infection in a developed country.Subjects and Setting: Overall 4742 subjects, aged 12-64, from Northern Ireland were randomly selected.Methods: Helicobacter pylori specific IgG antibodies were measured by enzyme linked immunosorbent assay, using an acid-glycine extract antigen, in stored serum from subjects who had participated in three linked population-based surveys of cardiovascular risk factors performed in 1986 and 1987.Results: The overall prevalence of H. pylori infection was 50.5%. Prevalence increased with age from 23.4% in 12-14 year olds to 72.7% in 60-64 year olds: chi 2 for trend 518, P < 10(-4). In subjects aged > or = 25, infection was more common in males (60.9%) than females (55.2%): chi 2 = 9.53, P < 0.01. This relation remained significant after adjusting for age, and measures of socioeconomic class: odds ratio (OR) for infection, male versus female was 1.19 (95% confidence interval [CI]: 1.02-1.40). Infection was associated with social class: the adjusted OR of infection in subjects from manual social classes relative to those from non-manual classes was 1.7 (95% CI: 1.47-1.98). Infection was significantly more common in current smokers and ex-smokers than in subjects who had never smoked: adjusted OR for infection, ex-smokers versus never smoked was 1.22 (95% CI: 1.01-1.49); for smokers of > or = 20/day versus never smoked OR = 1.33 (95% CI: 1.05-1.67). Infection was not associated with height in adult males but mean height in infected women was lower than in uninfected women after adjusting for age and socioeconomic status: difference in mean height (SE), -0.85 cm (0.32), P < 0.01. There was no demonstrable relationship between H. pylori infection and current alcohol intake.Conclusions: This study demonstrated a high prevalence of infection in a population from a developed country. Previously reported associations between H. pylori infection, age, sex, social class, and reduced height in females were confirmed and smoking was identified as a possible risk factor for H. pylori infection. [ABSTRACT FROM AUTHOR]- Published
- 1997
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26. Physical fitness, lipids, and apolipoproteins in the Northern Ireland Health and Activity Survey.
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MacAuley D, McCrum EE, Stott G, Evans AE, Duly E, Trinick TR, Sweeney K, and Boreham CAB
- Published
- 1997
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27. Physical activity, lipids, apolipoproteins, and Lp(a) in the Northern Ireland Health and Activity Survey.
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MacAuley D, McCrum EE, Stott G, Evans AE, Duly E, Trinick TR, Sweeney K, and Boreham CAG
- Published
- 1996
28. Janeway Lecture: Pediatric cancer treatment: a model for oncology
- Author
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Evans Ae
- Subjects
medicine.medical_specialty ,Chemotherapy ,Radiation Therapist ,business.industry ,General surgery ,medicine.medical_treatment ,MEDLINE ,Infant ,General Medicine ,Pediatric cancer ,Wilms Tumor ,Kidney Neoplasms ,Surgery ,Natural history ,Child, Preschool ,Pediatric oncology ,Medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,business ,Radiation treatment planning ,Child ,Survival rate - Abstract
Advances in pediatric oncology are reviewed using Wilms's tumor as a model. From the period when Wilms's tumor was treated by surgery alone to the time when adjuvant radiation and chemotherapy enabled attainment of an 80% survival rate, true collaboration among surgeons, radiation therapists, and pediatricians has been the key to success. The National Wilms's Tumor Study seeks to further refine treatment so that survival rates are maximized with minimum morbidity. The lessons applicable to all in cancer management are that a team approach is essential, all forms of treatment should be weighed early, treatment should be skilled and vigorous from the beginning the biology and natural history of the tumor should be considered in treatment planning, and toxicities of all forms of treatment should be respected and ways designed for their reduction.
- Published
- 1976
29. Multiagent chemotherapy for children with metastatic neuroblastoma: a report from Childrens Cancer Study Group
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Hammond D, J. Grosfeld, Robert E. Hittle, Samuel McCreadie, Sanford L. Leikin, J Z Finklestein, H N Sather, John M. Weiner, Evans Ae, I. Bernstein, and Klemperer M
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Oncology ,Cancer Research ,medicine.medical_specialty ,Vincristine ,Cyclophosphamide ,Adolescent ,medicine.medical_treatment ,Antineoplastic Agents ,Neuroblastoma ,Pharmacotherapy ,Actuarial Analysis ,Internal medicine ,medicine ,Humans ,Neoplasm Metastasis ,Child ,Imidazole carboxamide ,Chemotherapy ,business.industry ,Imidazoles ,Cancer ,Infant ,Multimodal therapy ,medicine.disease ,Surgery ,Doxorubicin ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,Drug Therapy, Combination ,business ,medicine.drug - Abstract
During the past 10-15 years there has not been a significant improvement in the overall survival of children with metastatic neuroblastoma. From 1971 through 1975, 104 eligible patients were entered on two clinical studies for newly diagnosed cases of stage IV neuroblastoma by the Childrens Cancer Study Group (CCSG). Patient data from both studies were evaluated for activity of cyclophosphamide, imidazole carboxamide, and vincristine and of these same agents plus adriamycin. Response was evaluated by serial measurements of tumor size. Eighty-four patients experienced a complete or partial response. The life-table estimate of median survival on both studies was 11–12 months for all patients and 13-18 months for responders, unchanged from the results of previous CCSG studies. Long-term survival, however, for patients on these studies demonstrates a significant increase compared with results reported from the three previous CCSG studies. Children less than 1 year or greater than 6 years of age at diagnosis showed a significantly improved survival pattern over the intermediate age group. It is suggested that there is a need to consider the induction response pattern and age at diagnosis when planning a maintenance program so that nonresponders can be identified early and considered for treatment with new agents or aggressive multimodal therapy.
- Published
- 1979
30. Your voice. Tongue-tied.
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Evans AE, Coryllos E, Abel JR, Schwartz RH, and Martin MS
- Published
- 2008
31. The Right Bite program: a theory-based nutrition intervention at a minority college campus.
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Evans AE and Sawyer-Morse MK
- Published
- 2002
32. The common thermolabile variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
- Author
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Harmon, DL, Woodside, JV, Yarnell, JW, McMaster, D, Young, IS, McCrum, EE, Gey, KF, Whitehead, AS, and Evans, AE
- Published
- 1996
33. Vitamin B6 status, MTHFR and hyperhomocysteinaemia
- Author
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Woodside, JV, Yarnell, JW, McMaster, D, Young, IS, McCrum, EE, Evans, AE, Gey, KF, Harmon, DL, and Whitehead, AS
- Published
- 1997
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34. Awareness and control of hypertension and hypercholesterolaemia in France and Northern Ireland
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Marques-Vidal, P, Evans, AE, Cambou, JP, Arveiler, D, Luc, G, Bingham, A, and Cambien, F
- Published
- 1997
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35. Total radical trapping antioxidant potential (TRAP) and exercise
- Author
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Sharpe, PC, Duly, EB, MacAuley, D, McCrum, EE, Mulholland, C, Stott, G, Boreham, CA, Kennedy, G, Evans, AE, and Trinick, TR
- Published
- 1996
36. Clarifying concepts about macronutrients' effects on satiation and satiety.
- Author
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Gerstein DE, Woodward-Lopez G, Evans AE, Kelsey K, and Drewnowski A
- Published
- 2004
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37. Factors of fruit and vegetable intake by race, gender, and age among young adolescents.
- Author
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Granner ML, Sargent RG, Calderon KS, Hussey JR, Evans AE, and Watkins KW
- Abstract
OBJECTIVE: To explore demographic differences in individual, social, and environmental factors potentially related to fruit and vegetable intake. DESIGN: Self-report questionnaires administered to a convenience sample of middle school students during regular classes. PARTICIPANTS: Black and white adolescents, 11 to 15 years of age (N = 736). VARIABLES MEASURED: Measures included self-efficacy, family dinner frequency, normative beliefs, outcome expectations, modeling, availability, preferences, snack choice, and demographics. ANALYSIS: Chi-square, general linear models, and Poisson and linear regressions as appropriate. RESULTS: Black participants reported greater social influences than did white participants, whereas white adolescents reported greater family environmental influences on fruit and vegetable intake. The oldest adolescents reported lower self-efficacy, peer modeling, family dinner frequency, and fruit and vegetable preferences compared with younger adolescents. White participants and females reported a higher preference for vegetables than did black participants and males. Regression models for self-efficacy and snack choice explained 41% and 34% of the variance, respectively. Preferences for vegetables and parental modeling were the strongest correlates of self-efficacy. Self-efficacy was the strongest correlate of snack choice. CONCLUSIONS AND IMPLICATIONS: Decreases in several factors with age highlight the importance of intervention for this age group. Future research is needed for a better understanding of the formation and modification of self-efficacy and snack choice. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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38. Heterogeneity in Pancreatitis: Recognizing Heterogeneity and Its Role in the Management of Pancreatitis. Summary of a National Institute of Diabetes and Digestive and Kidney Diseases Workshop.
- Author
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Bellin MD, Andersen DK, Akshintala V, Born D, Coghill RC, Easler J, Fogel EL, Forsmark CE, Freeman AJ, Hughes SJ, Jensen A, Liran O, Martin L, Pandol SJ, Palermo TM, Papachristou GI, Park WG, Phillips AE, Schwarzenberg SJ, Singh VK, Toledo FGS, VanDalfsen J, Whitcomb DC, Wu B, and Yadav D
- Abstract
Abstract: Both the clinical management and study of recurrent acute pancreatitis (RAP) and chronic pancreatitis (CP) is complicated by significant heterogeneity in the etiology, mechanisms, symptoms, and complications of pancreatitis. The National Institutes of Diabetes and Digestive and Kidney Disease (NIDDK) recently convened a workshop to address current knowledge and knowledge gaps in the field. Preclinical models that better replicate human disease are important for development of new therapies. Pain is often the most common and most difficult symptom to treat, as the causes are multifactorial and effective treatment may vary depending on whether pain is neuropathic or nociceptive in origin, and the placebo effect can complicate evaluation of the efficacy of medical and procedural interventions. Novel technologies like functional MRI and virtual reality may offer novel means for assessing and treating pain, respectively. Clinical trial designs will need to consider best approaches to addressing the heterogeneity of CP, including careful attention to designing eligibility criteria, and establishing accepted and validated core outcomes criteria for the field. The latter may be informed by consensus in pain research. Recruitment of participants into clinical trials has been challenging, often requiring multiple centers. Establishment of a clinical trials network would facilitate greater opportunities for therapeutic trials in pancreatitis., Competing Interests: Conflict of Interest: DY is a consultant for Pfizer, Inc. and has received research support from Abbvie Pharmaceuticals., (Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.)
- Published
- 2024
- Full Text
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39. Regulation of autophagy by Rab27B in colorectal cancer.
- Author
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Afroz S, Preet R, Vishwakarma V, Evans AE, Magstadt AN, and Dixon DA
- Subjects
- Humans, Animals, Mice, Cell Line, Tumor, Cell Proliferation genetics, Lysosomes metabolism, Lysosomes genetics, Mice, Nude, Autophagy genetics, rab GTP-Binding Proteins metabolism, rab GTP-Binding Proteins genetics, Colorectal Neoplasms pathology, Colorectal Neoplasms genetics, Colorectal Neoplasms metabolism
- Abstract
Autophagy is a cellular recycling process that is associated with tumor growth, anti-tumor immune responses, and therapy resistance in colorectal cancer (CRC). In this report, we identify the small GTPase Rab27B to control the autophagy process in CRC. Depletion of Rab27B showed an abnormal accumulation of autophagy vesicles and increased autophagy markers in CRC cells, indicating autophagy dysregulation. Image analysis indicated that autophagy flux is blocked at the autophagosome/lysosome fusion step when Rab27B is lost. While Rab27B deficient cells are proficient at growth under 2D in vitro conditions, cell growth was significantly impacted in both in vitro 3D growth and in vivo tumorigenesis studies. Together, these results demonstrate a new role of Rab27B in the autophagy trafficking process in CRC and identify Rab27B as a potential therapeutic target for CRC., Competing Interests: Declaration of Competing Interest The authors declare no competing interests., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2024
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40. The emerging invasive species and climate-change lexicon.
- Author
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Fusco EJ, Falk BG, Heimowitz PJ, Lieurance D, Parsons EW, Rottler CM, Thurman LL, and Evans AE
- Subjects
- Animals, Conservation of Natural Resources, Climate Change, Introduced Species, Terminology as Topic
- Abstract
The rapid diversification of terminology associated with invasion ecology is a known barrier to effective communication and management. These challenges are magnified by the addition of terms and concepts related to climate-induced range-shifting taxa and/or changes to impacts. Further, institutional policies and terminologies for invasive species introduce new ambiguities when considering climate change. To alleviate communication and application challenges, we introduce a conceptual framework that organizes climate-related invasion terms, revealing ambiguities and gaps. Additionally, we illustrate how these ambiguities can affect management with four case studies and consider situations where resolution can improve policy and management outcomes. The framework can help users avoid inconsistent use of terminology, and prioritize when to address management and policy consequences related to associated terminological ambiguity., Competing Interests: Declaration of interests No interests are declared., (Copyright © 2024 Elsevier Ltd. All rights reserved.)
- Published
- 2024
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41. Proton-Pump Inhibitors and Fat Absorption in Cystic Fibrosis and Pancreatic Insufficiency: A Randomized Crossover Pilot Trial.
- Author
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Phillips AE, Brownell JN, Tindall A, Kiernan BD, Patel D, Gelfond D, and Stallings VA
- Abstract
Background: Dietary fat malabsorption contributes to poor nutritional status in patients with cystic fibrosis (CF) and exocrine pancreatic insufficiency (EPI). Prescribing gastric acid-reducing agents such as proton-pump inhibitors (PPI) as an adjunct to pancreatic enzyme replacement therapy (PERT) to improve dietary fat absorption has been accepted in clinical practice despite limited evidence., Aims: This was a pilot randomized, double-blind, placebo-controlled crossover trial of subjects aged 12 and older with CF and EPI assessed on placebo and omeprazole to determine if PPI improved the efficacy of PERT as indicated by measures of dietary fat absorption., Methods: Fat malabsorption via stool coefficient of fat absorption (CFA) and malabsorption blood test (MBT), gastrointestinal pH (wireless motility capsule [WMC]), and quality of life (QOL) were assessed after 14 days on both placebo or PPI (omeprazole)., Results: Total 19 subjects enrolled, 13 were randomized, and 9 provided paired results on placebo and PPI. The 3 subject results for CFA were as follows: 1 increased, 1 decreased, and 1 was within the reference range in both tests for fat absorption. For 9 MBT subjects, 7 decreased and 2 increased fat absorption. For the 4 WMC studies, no change in transit times, nor in pH profiles were noted. No differences were seen in the domains of the two QOL questionnaires comparing placebo and PPI., Conclusions: These limited descriptive pilot study results in participants with CF and EPI on PERT evaluated by stool, blood, and QOL tests did not suggest improvement in fat absorption attributable to PPI., Competing Interests: Declarations Conflict of interest All authors disclose they have no conflicts of interest related to this project and manuscript. The funding sources had no role in study design, analysis, or drafting of the manuscript., (© 2024. The Author(s).)
- Published
- 2024
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42. Behavioral Health Support Specialists.
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Cuellar AE
- Subjects
- Humans, Mental Disorders therapy, Specialization, Mental Health Services
- Published
- 2024
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43. Individualized Pain Treatment in Chronic Pancreatitis (INPAIN): An International, Multicenter, Investigator-Initiated, Prospective, Cohort Study.
- Author
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Hagn-Meincke R, Dugic A, Agarwal A, Phillips AE, Waage A, Yadav D, Pillai D, Vivian E, de-Madaria E, Niazi IK, Easler J, Frøkjær JB, McNabb-Baltar J, Asferg LK, Faghih M, Montiel MBG, Cook M, Unnisa M, Tarnasky P, Hegyi P, Garg P, Nedergaard RB, Edwards R, Talukdar R, Farheen S, Olesen SS, Jagannath S, Schmidt S, Singh V, Hajnády Z, and Drewes AM
- Subjects
- Humans, Prospective Studies, Longitudinal Studies, Male, Female, Adult, Research Design, Treatment Outcome, Phenotype, Middle Aged, Abdominal Pain etiology, Abdominal Pain therapy, Abdominal Pain diagnosis, Pancreatitis, Chronic complications, Pancreatitis, Chronic therapy, Pancreatitis, Chronic diagnosis, Pain Measurement methods, Precision Medicine methods, Pain Management methods
- Abstract
Objectives: Pain is the foremost complication of chronic pancreatitis (CP), affecting about 70% of patients. However, the pathophysiological understanding and management of CP-related pain are complex, likely as patients have diverse "pain phenotypes" responding differently to treatment. This study aims to develop a bedside test panel to identify distinct pain phenotypes, investigate the temporal evolution, and determine whether they can be used to predict treatment response., Methods: The INPAIN study is an international, multicenter, observational, longitudinal cohort study consisted of 4 substudies. The studies will prospectively enroll 400 CP patients (50 without pain and 350 with pain) and 50 control subjects, conducting biannual observations for 4 years. The test panel is consisted of comprehensive subjective and objective assessment parameters. Statistical analysis strategies differ across the substudies. A model to predict treatment efficacy will be developed using various machine learning techniques, including an artificial intelligence approach, with internal cross-validation. Trajectories in pain parameters will be characterized by graphical analysis and mixed effect models., Discussion: The INPAIN study aims to comprehensively understand pain in CP through a test panel developed for routine clinical use. This tool has the potential to personalize treatments, improve clinical practice, enhance patient care, improve quality of life, and minimize treatment side effects., Competing Interests: The authors declare no conflict of interest., (Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.)
- Published
- 2025
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44. Natural history of spontaneous pancreatic portal vein fistulae: A systematic review of the literature.
- Author
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Griffin NE, Ferrell M, Feldman R, Dasyam AK, Slivka A, Khalid A, Singh H, Gabbert C, Das R, Mahmood S, Rabinovitz M, Chennat J, Romutis S, Klem ML, Yadav D, and Phillips AE
- Subjects
- Humans, Male, Middle Aged, Female, Vascular Fistula complications, Vascular Fistula diagnostic imaging, Portal Vein diagnostic imaging, Portal Vein pathology, Pancreatic Fistula etiology, Pancreatic Fistula epidemiology
- Abstract
Background: Spontaneous pancreatic portal vein fistula (PPVF) - a rare complication of pancreatic inflammation - varies widely in presentation and means of diagnosis but has been previously associated with bleeding complications and mortality. A systematic review of published literature was performed to assess the frequency of outcomes., Methods: A search of electronic databases (PubMed, Ovid MEDLINE, Scopus, EMBASE, gray literature) resulted in 1667 relevant unique manuscripts; 52 met inclusion criteria., Results: A total of 74 unique (male n = 47, 63.5 %) patients were included. Mean age was 53.5 (±11.9) years. History of alcohol use was reported in 55 (74.3 %). Underlying chronic pancreatitis (CP) was present in 49 (66.2 %). In cases where presenting symptoms were reported (n = 57, 77.4 %), the most frequent were abdominal pain (63.5 %), weight loss (14.9 %), rash (12.2 %), nausea/vomiting (12.2 %), and polyarthritis (9.5 %). Computed tomography was the most common imaging modality used to confirm the diagnosis (n = 20, 27.0 %), followed by magnetic resonance cholangiopancreatography (n = 14, 18.9 %). Portal vein thrombosis was reported in 57 (77.0 %), and bleeding events (luminal, variceal, or intra-pseudocyst) were reported in 13(17.6 %) patients. Younger age was associated with higher risk of bleeding events. Mortality was reported in 12 (16.2 %) patients at any time during follow up. Older age and polyarthritis at presentation were associated with mortality., Conclusions: PPVF is a rare and potentially fatal condition, though rates of bleeding complication and death were relatively low in this population. High-quality observational studies are needed to better understand the pathophysiology and natural history of this diagnosis., Competing Interests: Declaration of competing interest AEP: Board Member, National Pancreas Foundation. All other authors declare no relevant conflicts of interest., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
- Full Text
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45. Prevalence of exocrine pancreatic insufficiency at 12 months after acute pancreatitis: a prospective, multicentre, longitudinal cohort study.
- Author
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Phillips AE, Bejjani J, Culp S, Chennat J, Lee PJ, Machicado JD, Singh VK, Afghani E, Ramsey ML, Paragomi P, Stello K, Nikahd M, Hart PA, and Papachristou GI
- Abstract
Background: Exocrine Pancreatic insufficiency (EPI) occurs following acute pancreatitis (AP) at variably reported rates and with unclear recovery timeline. The aim of this study was to establish the prevalence and predictors of EPI at 12 months after AP in a prospective cohort., Methods: In this prospective, multicentre, longitudinal cohort study, adult participants (≥18 years) admitted to the hospital with an AP attack (defined by Revised Atlanta Classification) were enrolled in a United States multi-centre longitudinal cohort (Sites: The Ohio State University, University of Pittsburgh, and Johns Hopkins University). Patients were excluded if they had pancreatic cancer, chronic pancreatitis, or malabsorptive disease (including previously diagnosed EPI). Participant data was obtained by interview and by review of the electronic medical record. EPI was assessed by stool fecal elastase (FE-1) levels collected at baseline, 3 months, and 12 months (primary endpoint). EPI was defined by FE-1 <200 μg/g; severe FE-1 level ≤100 μg/g; mild FE-1 101-200 μg/g. Multivariable logistic regression was used to identify predictors of EPI at 12 months. This study is registered with ClinicalTrials.gov, NCT03063398., Findings: EPI was observed in 29 (34.1%) of the 85 participants [44 (51.8%) male, mean age 54.7 ± 14.1 years] who provided stool samples at 12 months. For the study overall, participants were recruited between June 22, 2017 and October 18, 2021. A total of 5794 individuals were screened, 311 of whom were eligible for the study. 112 participants provided stool samples at baseline, 79 completed stool samples at 3 months, and 85 completed samples at 12 months. 64 participants included samples at all 3 timepoints. In univariable analysis, factors significantly associated with EPI at 12 months included recurrent (versus index) AP, pre-existing diabetes, alcohol, and idiopathic etiologies, and increasing severity of AP. In multivariable analysis, the odds of having EPI at 12 months increased 4-fold with idiopathic AP etiology (Odds Ratio 4.095, 95% Confidence Interval [CI] 1.418, 11.826), and 3-fold with moderately severe or severe AP (Odds Ratio 3.166, 95% CI 1.156, 8.670), and baseline diabetes mellitus (Odds Ratio 3.217, 95% CI 1.113, 9.298). Even individuals with an index mild attack of AP (n = 39) developed severe EPI at 12 months (prevalence 12.8%)., Interpretation: EPI as diagnosed by FE-1 is present in over one third of prospectively assessed patients at 12 months post-AP. Since EPI develops in patients with mild AP, investigations are needed to understand the mechanisms of injury and identify methods for tailored screening., Funding: This study was supported by an Investigator Initiated Research Grant from AbbVie, Inc., Competing Interests: VKS declares being a Consultant to Ariel Precision Medicine, Panafina, and Horizon Therapeutics; a Scientific Advisory Board Member of and equity holder in Kyttaro, Origin Endoscopy and Solv Endotherapy. SC declares funding for research, including salary, paid to her institution by Abbvie. MLR declares support from the Cystic Fibrosis Foundation and the American Society for Parenteral and Enteral Nutrition, and position as Chair for the Young Trainees Committee for the Collaborative Alliance for Pancreatic Education and Research (CAPER). PJL declares the Investigator Initiated Research funding from Abbvie for the project execution and administration. GIP declares the Investigator Initiated Research funding that supported this study from Abbvie. All other authors declare no financial or other conflicts of interest., (© 2024 The Authors.)
- Published
- 2024
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46. Plasma-Derived Extracellular Vesicles and Non-Extracellular Vesicle Components from APC Min/+ Mice Promote Pro-Tumorigenic Activities and Activate Human Colonic Fibroblasts via the NF-κB Signaling Pathway.
- Author
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Arteaga-Blanco LA, Evans AE, and Dixon DA
- Subjects
- Animals, Humans, Mice, Adenomatous Polyposis Coli Protein metabolism, Adenomatous Polyposis Coli Protein genetics, Cancer-Associated Fibroblasts metabolism, Cancer-Associated Fibroblasts pathology, Carcinogenesis pathology, Carcinogenesis genetics, Carcinogenesis metabolism, Colon pathology, Colon metabolism, Colorectal Neoplasms pathology, Colorectal Neoplasms metabolism, Colorectal Neoplasms genetics, Cytokines metabolism, Mice, Inbred C57BL, Tumor Microenvironment, Extracellular Vesicles metabolism, Fibroblasts metabolism, NF-kappa B metabolism, Signal Transduction
- Abstract
Colorectal cancer (CRC) is the third most prevalent cancer worldwide. Current studies have demonstrated that tumor-derived extracellular vesicles (EVs) from different cancer cell types modulate the fibroblast microenvironment to contribute to cancer development and progression. Here, we isolated and characterized circulating large EVs (LEVs), small EVs (SEVs) and non-EV entities released in the plasma from wild-type (WT) mice and the APC
Min/+ CRC mice model. Our results showed that human colon fibroblasts exposed from APC-EVs, but not from WT-EVs, exhibited the phenotypes of cancer-associated fibroblasts (CAFs) through EV-mediated NF-κB pathway activation. Cytokine array analysis on secreted proteins revealed elevated levels of inflammatory cytokine implicated in cancer growth and metastasis. Finally, non-activated cells co-cultured with supernatant from fibroblasts treated with APC-EVs showed increased mRNA expressions of CAFs markers, the ECM, inflammatory cytokines, as well as the expression of genes controlled by NF-κB. Altogether, our work suggests that EVs and non-EV components from APCMin/+ mice are endowed with pro-tumorigenic activities and promoted inflammation and a CAF-like state by triggering NF-κB signaling in fibroblasts to support CRC growth and progression. These findings provide insight into the interaction between plasma-derived EVs and human cells and can be used to design new CRC diagnosis and prognosis tools.- Published
- 2024
- Full Text
- View/download PDF
47. Alterations in exocrine pancreatic function after acute pancreatitis.
- Author
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Bejjani J, Ramsey ML, Lee PJ, Phillips AE, Singh VK, Yadav D, Papachristou GI, and Hart PA
- Subjects
- Humans, Exocrine Pancreatic Insufficiency physiopathology, Exocrine Pancreatic Insufficiency etiology, Acute Disease, Pancreatitis physiopathology, Pancreatitis complications, Pancreas, Exocrine physiopathology
- Abstract
Exocrine pancreatic dysfunction (EPD) is a malabsorptive complication of pancreatic disorders that can lead to a host of symptoms ranging from flatulence to diarrhea and contribute to weight loss and metabolic bone disease. It is increasingly recognized to occur after acute pancreatitis (AP), including episodes with mild severity. The risk of developing EPD after AP is influenced by a range of factors, including the degree of acinar cell destruction and inflammation during AP, and persistent structural derangements following AP. In this article, we discuss the epidemiology, pathophysiology, and clinical management of EPD after AP while highlighting key knowledge gaps., Competing Interests: Declaration of competing interest No conflicts of interest exist., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
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- 2024
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48. Analgesia for the treatment of acute pancreatitis: a protocol for a systematic review and network meta-analysis.
- Author
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Subramani SS, Berg AC, Kral LA, Murad MH, Smith A, Phillips AE, Yadav D, Uc A, and Imdad A
- Subjects
- Humans, Analgesics therapeutic use, Research Design, Acute Disease, Analgesia methods, Randomized Controlled Trials as Topic, Analgesics, Opioid therapeutic use, Systematic Reviews as Topic, Pancreatitis drug therapy, Pancreatitis therapy, Network Meta-Analysis, Pain Management methods
- Abstract
Introduction: Gastrointestinal hospitalisations in the USA cause over US$130 billion in expenditures, and acute pancreatitis is a leading cause of these hospitalisations. Adequate pain control is one of the primary treatment goals for acute pancreatitis. Though opioids are commonly used for analgesia in these patients, there have been concerns about short-term and long-term side effects of using opioids. Recently, non-opioid medications have been studied to treat pain in patients with acute pancreatitis. This systematic review and network meta-analysis aims to assess the comparative efficacy of analgesic medication for non-severe, acute pancreatitis., Methods and Analysis: We will search multiple electronic databases for randomised controlled trials that study pain management in patients with non-severe, acute pancreatitis. The intervention will be any analgesic for acute pancreatitis in the hospital setting. The comparison group will be patients who received a placebo or other active interventions for pain management. The primary outcomes of interest include pain scores and the need for supplementary analgesia. The secondary outcomes will be serious adverse events, local complications, progression to severe pancreatitis, transfer to the intensive care unit, length of hospitalisation, time to start enteral feeds, 30-day all-cause mortality and Quality of Life Scale scores. If sufficient homogeneity exists among included studies, the findings will be pooled using a traditional pairwise and network meta-analysis. The risk of bias in randomised control trials will be evaluated using the Cochrane Risk of Bias Tool 2.0. The Grading of Recommendations, Assessment, Development, and Evaluation approach will be used to report the certainty of evidence., Ethics and Dissemination: This systematic review will not involve direct contact with human subjects. The findings of this review will be published in a peer-reviewed journal. They will give healthcare providers a better awareness of the optimal analgesic medication for pain treatment in non-severe, acute pancreatitis., Competing Interests: Competing interests: None declared., (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
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- 2024
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49. Clinical diagnosis of psychiatric comorbidities, performance of screening tests and pattern of psychotropic medication use in patients with chronic pancreatitis.
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Griffin NE, Feldman R, Althouse AD, Yadav D, and Phillips AE
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- Adult, Humans, Male, Female, Middle Aged, Aged, Comorbidity, Anxiety epidemiology, Benzodiazepines, Psychotropic Drugs therapeutic use, Pancreatitis, Chronic epidemiology
- Abstract
Background: Psychiatric comorbidity measured by screening instruments is common in patients with chronic pancreatitis (CP) but whether this accurately reflects clinical diagnosis of psychiatric comorbidity is unknown and the prevalence of psychotropic medication prescription in CP remains largely unexplored., Methods: Adult patients (≥18 years) with definite CP were enrolled and completed the Hospital Anxiety and Depression Scale (HADS). Demographics, clinical characteristics and medications were retrieved from case report forms and the electronic health record (EHR). Clinical diagnosis of depression or anxiety was determined by presence of ICD-10 code or inclusion in the patient's EHR problem list or treatment plan. Comparisons were made between patients with and without clinical psychiatric comorbidity., Results: Total of 81 patients (48, 59.3% male; mean age 57.6 ± 14.3 years) were included. Clinical diagnoses of anxiety and depression were each noted in 47 (58%) patients, with overlap in 42 (51.9%). Compared to clinical diagnoses, the sensitivity and specificity of a positive screen for anxiety (HADS >7) were 76.6% and 91.2%; for depression 55.3% and 88.2%. Patients with anxiety and/or depression were more frequently female (51.9% v 20.7%), younger (53.6 v 64.9 years), and had alcohol etiology (51.9% v 27.6%) (all p < 0.01). In those with psychiatric comorbidity, 42 (80.8%) were prescribed psychotropic medication, most commonly gabapentinoid (24, 57.1%), selective serotonin reuptake inhibitor (n = 22, 52.4%) or benzodiazepine (n = 20, 47.6%)., Conclusions: Psychiatric comorbidities are common among CP patients and many receive psychotropic medications. Further studies are needed to evaluate the impact of these medications on CP symptoms., Competing Interests: Declaration of competing interest The authors report that they have no relevant conflicts of interest., (Copyright © 2024 IAP and EPC. Published by Elsevier B.V. All rights reserved.)
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- 2024
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50. Interventions for Pancreatitis-New Approaches, Knowledge Gaps, and Research Opportunities: Summary of a National Institute of Diabetes and Digestive and Kidney Diseases Workshop.
- Author
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Phillips AE, Hughes SJ, Andersen DK, Bell A, Brand R, Coté GA, Cowdin A, Diazgranados N, Dudeja V, Duggan SN, Fogel E, Forsmark CE, Freeman AJ, Gittes G, Hart PA, Jeon C, Nealon W, Neoptolemos J, Palermo TM, Pandol S, Roberts KM, Rosenthal M, Singh VK, Yadav D, Whitcomb DC, and Zyromski N
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- Humans, National Institute of Diabetes and Digestive and Kidney Diseases (U.S.), Pain, United States, Diabetes Mellitus diagnosis, Diabetes Mellitus therapy, Pancreatitis, Chronic therapy, Pancreatitis, Chronic drug therapy
- Abstract
Abstract: There exists no cure for acute, recurrent acute or chronic pancreatitis and treatments to date have been focused on managing symptoms. A recent workshop held by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) focused on interventions that might disrupt or perhaps even reverse the natural course of this heterogenous disease, aiming to identify knowledge gaps and research opportunities that might inform future funding initiatives for NIDDK. The breadth and variety of identified active or planned clinical trials traverses the spectrum of the disease and was conceptually grouped for the workshop into behavioral, nutritional, pharmacologic and biologic, and mechanical interventions. Cognitive and other behavioral therapies are proven interventions for pain and addiction, but barriers exist to their use. Whilst a disease specific instrument quantifying pain is now validated, an equivalent is lacking for nutrition - and both face challenges in ease and frequency of administration. Multiple pharmacologic agents hold promise. Ongoing development of Patient Reported Outcome (PRO) measurements can satisfy Investigative New Drug (IND) regulatory assessments. Despite multiple randomized clinical trials demonstrating benefit, great uncertainty remains regarding patient selection, timing of intervention, and type of mechanical intervention (endoscopic versus surgery). Challenges and opportunities to establish beneficial interventions for patients were identified., Competing Interests: All other authors report no relevant financial or other conflicts of interest. Disclosures: The following authors disclose potential conflicts of interest: A.E.P. (board member, National Pancreas Foundation), R.B. (board member, National Pancreas Foundation), G.C. (consultant, Olympus America; consultant, Interpace Diagnostics; scientific advisory board, Genprex), S.D. (corecipient of unrestricted industry research funding from Mylan Healthcare, expert panel for Mylan Healthcare), A.F. (consultant work for Takeda and Abbvie), C.F. (board member, National Pancreas Foundation; research support, Abbvie), M.R. (honoraria from Fresenius Kabi as speaker); V.S. (board member, National Panreas Foundation; consultant to Abbvie, Ariel Precision Medicine, Organon, Nestle Health Sciences, Panafina, and Horizon Therapeutics; scientific advisory board member and equity holder in Kyttaro and Origin Endoscopy), D.W. (consultant to Abbvie, Ariel Precision Medicine, Nestle, Organon, Regeneron; cofounder and chief scientific officer, Ariel Precision Medicine), and D.Y. (consultant, Pfizer Inc)., (Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.)
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- 2024
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