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Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden

OBJECTIVE: To determine if low psychosocial stress resilience in adolescence (increasing chronic stress arousal throughout life) is associated with an increased inflammatory bowel disease (IBD) risk in adulthood. Subclinical Crohn's disease (CD) and ulcerative colitis (UC) can exist over many y...

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Autores principales: Melinder, Carren, Hiyoshi, Ayako, Fall, Katja, Halfvarson, Jonas, Montgomery, Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278277/
https://www.ncbi.nlm.nih.gov/pubmed/28130207
http://dx.doi.org/10.1136/bmjopen-2016-014315
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author Melinder, Carren
Hiyoshi, Ayako
Fall, Katja
Halfvarson, Jonas
Montgomery, Scott
author_facet Melinder, Carren
Hiyoshi, Ayako
Fall, Katja
Halfvarson, Jonas
Montgomery, Scott
author_sort Melinder, Carren
collection PubMed
description OBJECTIVE: To determine if low psychosocial stress resilience in adolescence (increasing chronic stress arousal throughout life) is associated with an increased inflammatory bowel disease (IBD) risk in adulthood. Subclinical Crohn's disease (CD) and ulcerative colitis (UC) can exist over many years and we hypothesise that psychosocial stress may result in conversion to symptomatic disease through its proinflammatory or barrier function effects. DESIGN: National register-based cohort study of men followed from late adolescence to middle age. SETTING: A general population cohort of men in Sweden. PARTICIPANTS: Swedish population-based registers provided information on all men born between 1952 and 1956 who underwent mandatory Swedish military conscription assessment (n=239 591). Men with any gastrointestinal diagnoses (except appendicitis) prior to follow-up were excluded. PRIMARY OUTCOME MEASURES: An inpatient or outpatient diagnosis of CD or UC recorded in the Swedish Patient Register (1970–2009). RESULTS: A total of 938 men received a diagnosis of CD and 1799 UC. Lower stress resilience in adolescence was associated with increased IBD risk, with unadjusted HRs (95% CIs) of 1.54 (1.26 to 1.88) and 1.24 (1.08 to 1.42), for CD and UC, respectively. After adjustment for potential confounding factors, including markers of subclinical disease activity in adolescence, they are 1.39 (1.13 to 1.71) and 1.19 (1.03 to 1.37). CONCLUSIONS: Lower stress resilience may increase the risk of diagnosis of IBD in adulthood, possibly through an influence on inflammation or barrier function.
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spelling pubmed-52782772017-02-07 Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden Melinder, Carren Hiyoshi, Ayako Fall, Katja Halfvarson, Jonas Montgomery, Scott BMJ Open Epidemiology OBJECTIVE: To determine if low psychosocial stress resilience in adolescence (increasing chronic stress arousal throughout life) is associated with an increased inflammatory bowel disease (IBD) risk in adulthood. Subclinical Crohn's disease (CD) and ulcerative colitis (UC) can exist over many years and we hypothesise that psychosocial stress may result in conversion to symptomatic disease through its proinflammatory or barrier function effects. DESIGN: National register-based cohort study of men followed from late adolescence to middle age. SETTING: A general population cohort of men in Sweden. PARTICIPANTS: Swedish population-based registers provided information on all men born between 1952 and 1956 who underwent mandatory Swedish military conscription assessment (n=239 591). Men with any gastrointestinal diagnoses (except appendicitis) prior to follow-up were excluded. PRIMARY OUTCOME MEASURES: An inpatient or outpatient diagnosis of CD or UC recorded in the Swedish Patient Register (1970–2009). RESULTS: A total of 938 men received a diagnosis of CD and 1799 UC. Lower stress resilience in adolescence was associated with increased IBD risk, with unadjusted HRs (95% CIs) of 1.54 (1.26 to 1.88) and 1.24 (1.08 to 1.42), for CD and UC, respectively. After adjustment for potential confounding factors, including markers of subclinical disease activity in adolescence, they are 1.39 (1.13 to 1.71) and 1.19 (1.03 to 1.37). CONCLUSIONS: Lower stress resilience may increase the risk of diagnosis of IBD in adulthood, possibly through an influence on inflammation or barrier function. BMJ Publishing Group 2017-01-27 /pmc/articles/PMC5278277/ /pubmed/28130207 http://dx.doi.org/10.1136/bmjopen-2016-014315 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology
Melinder, Carren
Hiyoshi, Ayako
Fall, Katja
Halfvarson, Jonas
Montgomery, Scott
Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden
title Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden
title_full Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden
title_fullStr Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden
title_full_unstemmed Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden
title_short Stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in Sweden
title_sort stress resilience and the risk of inflammatory bowel disease: a cohort study of men living in sweden
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278277/
https://www.ncbi.nlm.nih.gov/pubmed/28130207
http://dx.doi.org/10.1136/bmjopen-2016-014315
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