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Association between infections and functional somatic disorders: a cross-sectional population-based cohort study
OBJECTIVES: It has been suggested that infections can trigger functional somatic disorders (FSD). However, current evidence is limited by inconsistent findings in smaller studies conducted in clinical settings within selected populations and short follow-up times. We aimed to test the hypothesis tha...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639106/ https://www.ncbi.nlm.nih.gov/pubmed/36323461 http://dx.doi.org/10.1136/bmjopen-2022-066037 |
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author | Schovsbo, Signe Ulfbeck Møllehave, Line Tang Petersen, Marie Weinreich Ahrendt Bjerregaard, Anne Eliasen, Marie Pedersen, Susanne Brix Eplov, Lene Falgaard Kårhus, Line Lund Fink, Per Linneberg, Allan Dantoft, Thomas Meinertz Jørgensen, Torben Benros, Michael Eriksen |
author_facet | Schovsbo, Signe Ulfbeck Møllehave, Line Tang Petersen, Marie Weinreich Ahrendt Bjerregaard, Anne Eliasen, Marie Pedersen, Susanne Brix Eplov, Lene Falgaard Kårhus, Line Lund Fink, Per Linneberg, Allan Dantoft, Thomas Meinertz Jørgensen, Torben Benros, Michael Eriksen |
author_sort | Schovsbo, Signe Ulfbeck |
collection | PubMed |
description | OBJECTIVES: It has been suggested that infections can trigger functional somatic disorders (FSD). However, current evidence is limited by inconsistent findings in smaller studies conducted in clinical settings within selected populations and short follow-up times. We aimed to test the hypothesis that former infections are associated with FSD using data from nationwide registries and a large population-based cohort study, the Danish Study of Functional Disorders study. DESIGN: FSD cases were identified in a cross-sectional population-based cohort and linked retrospectively to former hospital contacts with infections identified in the Danish National Patient Registry. The associations between FSD and former infections within 17 years were analysed using logistic regressions to calculate ORs and 95% CIs adjusted for age, sex and subjective social status. SETTING: A population-based cohort in Denmark examined between 2011 and 2015. PARTICIPANTS: A total of 9656 men and women aged 18–76 years. MAIN OUTCOME MEASURES: FSD measured by various delimitations, including bodily distress syndrome (BDS), irritable bowel (IB), chronic fatigue (CF), chronic widespread pain (CWP), and multiple chemical sensitivity (MCS). RESULTS: Overall, infections were associated with increased risk of all delimitations of FSD. The associations were more pronounced for multisystemic FSD. The number of prior infections increased the risk in a dose-response manner (p<0.0001). Bacterial but not viral infections were significantly associated with BDS (OR 1.69 (95% CI 1.46 to 1.96)), IB (OR 1.41 (95% CI 1.06 to 1.88)), CWP (OR 1.47 (95% CI 1.13 to 1.90)) and CF (OR 1.62 (95% CI 1.34 to 1.96)), but not MCS. CONCLUSION: Former infections leading to hospital contacts were associated with a higher risk of having FSD. These associations were more pronounced for bacterial than viral infections, and more infections increased the risk in a dose-response manner. These results tend to support the idea that severe infections could play a role in FSD. |
format | Online Article Text |
id | pubmed-9639106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-96391062022-11-08 Association between infections and functional somatic disorders: a cross-sectional population-based cohort study Schovsbo, Signe Ulfbeck Møllehave, Line Tang Petersen, Marie Weinreich Ahrendt Bjerregaard, Anne Eliasen, Marie Pedersen, Susanne Brix Eplov, Lene Falgaard Kårhus, Line Lund Fink, Per Linneberg, Allan Dantoft, Thomas Meinertz Jørgensen, Torben Benros, Michael Eriksen BMJ Open Epidemiology OBJECTIVES: It has been suggested that infections can trigger functional somatic disorders (FSD). However, current evidence is limited by inconsistent findings in smaller studies conducted in clinical settings within selected populations and short follow-up times. We aimed to test the hypothesis that former infections are associated with FSD using data from nationwide registries and a large population-based cohort study, the Danish Study of Functional Disorders study. DESIGN: FSD cases were identified in a cross-sectional population-based cohort and linked retrospectively to former hospital contacts with infections identified in the Danish National Patient Registry. The associations between FSD and former infections within 17 years were analysed using logistic regressions to calculate ORs and 95% CIs adjusted for age, sex and subjective social status. SETTING: A population-based cohort in Denmark examined between 2011 and 2015. PARTICIPANTS: A total of 9656 men and women aged 18–76 years. MAIN OUTCOME MEASURES: FSD measured by various delimitations, including bodily distress syndrome (BDS), irritable bowel (IB), chronic fatigue (CF), chronic widespread pain (CWP), and multiple chemical sensitivity (MCS). RESULTS: Overall, infections were associated with increased risk of all delimitations of FSD. The associations were more pronounced for multisystemic FSD. The number of prior infections increased the risk in a dose-response manner (p<0.0001). Bacterial but not viral infections were significantly associated with BDS (OR 1.69 (95% CI 1.46 to 1.96)), IB (OR 1.41 (95% CI 1.06 to 1.88)), CWP (OR 1.47 (95% CI 1.13 to 1.90)) and CF (OR 1.62 (95% CI 1.34 to 1.96)), but not MCS. CONCLUSION: Former infections leading to hospital contacts were associated with a higher risk of having FSD. These associations were more pronounced for bacterial than viral infections, and more infections increased the risk in a dose-response manner. These results tend to support the idea that severe infections could play a role in FSD. BMJ Publishing Group 2022-11-02 /pmc/articles/PMC9639106/ /pubmed/36323461 http://dx.doi.org/10.1136/bmjopen-2022-066037 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Epidemiology Schovsbo, Signe Ulfbeck Møllehave, Line Tang Petersen, Marie Weinreich Ahrendt Bjerregaard, Anne Eliasen, Marie Pedersen, Susanne Brix Eplov, Lene Falgaard Kårhus, Line Lund Fink, Per Linneberg, Allan Dantoft, Thomas Meinertz Jørgensen, Torben Benros, Michael Eriksen Association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
title | Association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
title_full | Association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
title_fullStr | Association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
title_full_unstemmed | Association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
title_short | Association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
title_sort | association between infections and functional somatic disorders: a cross-sectional population-based cohort study |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639106/ https://www.ncbi.nlm.nih.gov/pubmed/36323461 http://dx.doi.org/10.1136/bmjopen-2022-066037 |
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