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Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study
Irritable bowel syndrome (IBS) affects up to 22% of the general population. Its aetiology remains unclear. Previously reported cross-sectional associations with psychological distress and depression are not fully understood. We hypothesised that psychosocial factors, particularly those associated wi...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441776/ https://www.ncbi.nlm.nih.gov/pubmed/17928145 http://dx.doi.org/10.1016/j.pain.2007.08.029 |
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author | Nicholl, B.I. Halder, S.L. Macfarlane, G.J. Thompson, D.G. O’Brien, S. Musleh, M. McBeth, J. |
author_facet | Nicholl, B.I. Halder, S.L. Macfarlane, G.J. Thompson, D.G. O’Brien, S. Musleh, M. McBeth, J. |
author_sort | Nicholl, B.I. |
collection | PubMed |
description | Irritable bowel syndrome (IBS) affects up to 22% of the general population. Its aetiology remains unclear. Previously reported cross-sectional associations with psychological distress and depression are not fully understood. We hypothesised that psychosocial factors, particularly those associated with somatisation, would act as risk markers for the onset of IBS. We conducted a community-based prospective study of subjects, aged 25–65 years, randomly selected from the registers of three primary care practices. Responses to a detailed questionnaire allowed subjects’ IBS status to be classified using a modified version of the Rome II criteria. The questionnaire also included validated psychosocial instruments. Subjects free of IBS at baseline and eligible for follow-up 15 months later formed the cohort for this analysis (n = 3732). An adjusted participation rate of 71% (n = 2456) was achieved at follow-up. 3.5% (n = 86) of subjects developed IBS. After adjustment for age, gender and baseline abdominal pain status, high levels of illness behaviour (odds ratio (OR) = 5.2; 95% confidence interval (95% CI) 2.5–11.0), anxiety (OR = 2.0; 95% CI 0.98–4.1), sleep problems (OR = 1.6; 95% CI 0.8–3.2), and somatic symptoms (OR = 1.6; 95% CI 0.8–2.9) were found to be independent predictors of IBS onset. This study has demonstrated that psychosocial factors indicative of the process of somatisation are independent risk markers for the development of IBS in a group of subjects previously free of IBS. Similar relationships are observed in other “functional” disorders, further supporting the hypothesis that they have similar aetiologies. |
format | Text |
id | pubmed-2441776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-24417762008-07-08 Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study Nicholl, B.I. Halder, S.L. Macfarlane, G.J. Thompson, D.G. O’Brien, S. Musleh, M. McBeth, J. Pain Article Irritable bowel syndrome (IBS) affects up to 22% of the general population. Its aetiology remains unclear. Previously reported cross-sectional associations with psychological distress and depression are not fully understood. We hypothesised that psychosocial factors, particularly those associated with somatisation, would act as risk markers for the onset of IBS. We conducted a community-based prospective study of subjects, aged 25–65 years, randomly selected from the registers of three primary care practices. Responses to a detailed questionnaire allowed subjects’ IBS status to be classified using a modified version of the Rome II criteria. The questionnaire also included validated psychosocial instruments. Subjects free of IBS at baseline and eligible for follow-up 15 months later formed the cohort for this analysis (n = 3732). An adjusted participation rate of 71% (n = 2456) was achieved at follow-up. 3.5% (n = 86) of subjects developed IBS. After adjustment for age, gender and baseline abdominal pain status, high levels of illness behaviour (odds ratio (OR) = 5.2; 95% confidence interval (95% CI) 2.5–11.0), anxiety (OR = 2.0; 95% CI 0.98–4.1), sleep problems (OR = 1.6; 95% CI 0.8–3.2), and somatic symptoms (OR = 1.6; 95% CI 0.8–2.9) were found to be independent predictors of IBS onset. This study has demonstrated that psychosocial factors indicative of the process of somatisation are independent risk markers for the development of IBS in a group of subjects previously free of IBS. Similar relationships are observed in other “functional” disorders, further supporting the hypothesis that they have similar aetiologies. Lippincott Williams & Wilkins 2008-06-30 /pmc/articles/PMC2441776/ /pubmed/17928145 http://dx.doi.org/10.1016/j.pain.2007.08.029 Text en © 2008 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license |
spellingShingle | Article Nicholl, B.I. Halder, S.L. Macfarlane, G.J. Thompson, D.G. O’Brien, S. Musleh, M. McBeth, J. Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study |
title | Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study |
title_full | Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study |
title_fullStr | Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study |
title_full_unstemmed | Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study |
title_short | Psychosocial risk markers for new onset irritable bowel syndrome – Results of a large prospective population-based study |
title_sort | psychosocial risk markers for new onset irritable bowel syndrome – results of a large prospective population-based study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441776/ https://www.ncbi.nlm.nih.gov/pubmed/17928145 http://dx.doi.org/10.1016/j.pain.2007.08.029 |
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