Functional dyspepsia in depression: A population‐based cohort study

Background Patients with functional dyspepsia (FD) are more likely to have persistent depression, yet whether depression and antidepressant treatments are associated with subsequent risk of FD remain unclear. Methods Using population‐based insurance administrative data of Taiwan, an 11‐year historic...

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Veröffentlicht in:European journal of clinical investigation 2021-06, Vol.51 (6), p.e13506-n/a
Hauptverfasser: Kao, Kai‐Liang, Sung, Fung‐Chang, Huang, Hui‐Chun, Lin, Chen‐Ju, Chen, Shu‐Chin, Lin, Cheng‐Li, Huang, Yo‐Ping, Wu, Shu‐I, Chen, Yi‐Shin, Stewart, Robert
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container_issue 6
container_start_page e13506
container_title European journal of clinical investigation
container_volume 51
creator Kao, Kai‐Liang
Sung, Fung‐Chang
Huang, Hui‐Chun
Lin, Chen‐Ju
Chen, Shu‐Chin
Lin, Cheng‐Li
Huang, Yo‐Ping
Wu, Shu‐I
Chen, Yi‐Shin
Stewart, Robert
description Background Patients with functional dyspepsia (FD) are more likely to have persistent depression, yet whether depression and antidepressant treatments are associated with subsequent risk of FD remain unclear. Methods Using population‐based insurance administrative data of Taiwan, an 11‐year historic cohort study was assembled, comparing cases aged 18 and above with the diagnosis of depressive disorder, to a propensity score‐matched sample of adults without depression. Incident FD as a primary diagnosis was ascertained. Hazard ratios of FD were calculated using Cox regression models by age, gender, other comorbidities, nonsteroidal anti‐inflammatory medications, antidepressants and antidiabetic agents. Results A total of 20,197 people with depressive disorder and 20,197 propensity score‐matched comparisons without depression were followed up. The incidence of FD was 1.7‐fold greater in the depressive cohort than in comparisons (12.9 versus 7.57 per 1000 person‐years), with an adjusted hazard ratio (aHR) of 2.16 (95% confidence interval (CI) 1.93~2.41). Increased risks were significant regardless of comorbidities or medication uses, the highest in the untreated depression group compared to the group without depression, with an aHR of 2.51(95% CI 2.15~2.93). Conclusions This population‐based study showed that patients with depressive disorder are at elevated risk of FD. Antidepressant treatment could reduce the risk of FD.
doi_str_mv 10.1111/eci.13506
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Methods Using population‐based insurance administrative data of Taiwan, an 11‐year historic cohort study was assembled, comparing cases aged 18 and above with the diagnosis of depressive disorder, to a propensity score‐matched sample of adults without depression. Incident FD as a primary diagnosis was ascertained. Hazard ratios of FD were calculated using Cox regression models by age, gender, other comorbidities, nonsteroidal anti‐inflammatory medications, antidepressants and antidiabetic agents. Results A total of 20,197 people with depressive disorder and 20,197 propensity score‐matched comparisons without depression were followed up. The incidence of FD was 1.7‐fold greater in the depressive cohort than in comparisons (12.9 versus 7.57 per 1000 person‐years), with an adjusted hazard ratio (aHR) of 2.16 (95% confidence interval (CI) 1.93~2.41). Increased risks were significant regardless of comorbidities or medication uses, the highest in the untreated depression group compared to the group without depression, with an aHR of 2.51(95% CI 2.15~2.93). Conclusions This population‐based study showed that patients with depressive disorder are at elevated risk of FD. Antidepressant treatment could reduce the risk of FD.</description><identifier>ISSN: 0014-2972</identifier><identifier>EISSN: 1365-2362</identifier><identifier>DOI: 10.1111/eci.13506</identifier><identifier>PMID: 33529347</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; antidepressant treatment ; Antidepressants ; Antidepressive Agents - therapeutic use ; Cohort analysis ; Cohort Studies ; Confidence intervals ; Depressive Disorder - drug therapy ; Depressive Disorder - epidemiology ; depressive disorders ; Diabetes mellitus ; Diagnosis ; Dyspepsia ; Dyspepsia - epidemiology ; Female ; functional dyspepsia ; Humans ; Incidence ; Inflammation ; Longitudinal studies ; longitudinal study ; Male ; Mental depression ; Middle Aged ; Population studies ; Population-based studies ; Propensity Score ; propensity score matching ; Proportional Hazards Models ; Regression analysis ; Regression models ; Risk ; Risk reduction ; Statistical analysis ; Taiwan - epidemiology</subject><ispartof>European journal of clinical investigation, 2021-06, Vol.51 (6), p.e13506-n/a</ispartof><rights>2021 Stichting European Society for Clinical Investigation Journal Foundation. 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Methods Using population‐based insurance administrative data of Taiwan, an 11‐year historic cohort study was assembled, comparing cases aged 18 and above with the diagnosis of depressive disorder, to a propensity score‐matched sample of adults without depression. Incident FD as a primary diagnosis was ascertained. Hazard ratios of FD were calculated using Cox regression models by age, gender, other comorbidities, nonsteroidal anti‐inflammatory medications, antidepressants and antidiabetic agents. Results A total of 20,197 people with depressive disorder and 20,197 propensity score‐matched comparisons without depression were followed up. The incidence of FD was 1.7‐fold greater in the depressive cohort than in comparisons (12.9 versus 7.57 per 1000 person‐years), with an adjusted hazard ratio (aHR) of 2.16 (95% confidence interval (CI) 1.93~2.41). Increased risks were significant regardless of comorbidities or medication uses, the highest in the untreated depression group compared to the group without depression, with an aHR of 2.51(95% CI 2.15~2.93). Conclusions This population‐based study showed that patients with depressive disorder are at elevated risk of FD. 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Methods Using population‐based insurance administrative data of Taiwan, an 11‐year historic cohort study was assembled, comparing cases aged 18 and above with the diagnosis of depressive disorder, to a propensity score‐matched sample of adults without depression. Incident FD as a primary diagnosis was ascertained. Hazard ratios of FD were calculated using Cox regression models by age, gender, other comorbidities, nonsteroidal anti‐inflammatory medications, antidepressants and antidiabetic agents. Results A total of 20,197 people with depressive disorder and 20,197 propensity score‐matched comparisons without depression were followed up. The incidence of FD was 1.7‐fold greater in the depressive cohort than in comparisons (12.9 versus 7.57 per 1000 person‐years), with an adjusted hazard ratio (aHR) of 2.16 (95% confidence interval (CI) 1.93~2.41). Increased risks were significant regardless of comorbidities or medication uses, the highest in the untreated depression group compared to the group without depression, with an aHR of 2.51(95% CI 2.15~2.93). Conclusions This population‐based study showed that patients with depressive disorder are at elevated risk of FD. Antidepressant treatment could reduce the risk of FD.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>33529347</pmid><doi>10.1111/eci.13506</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-8461-5613</orcidid></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Aged
antidepressant treatment
Antidepressants
Antidepressive Agents - therapeutic use
Cohort analysis
Cohort Studies
Confidence intervals
Depressive Disorder - drug therapy
Depressive Disorder - epidemiology
depressive disorders
Diabetes mellitus
Diagnosis
Dyspepsia
Dyspepsia - epidemiology
Female
functional dyspepsia
Humans
Incidence
Inflammation
Longitudinal studies
longitudinal study
Male
Mental depression
Middle Aged
Population studies
Population-based studies
Propensity Score
propensity score matching
Proportional Hazards Models
Regression analysis
Regression models
Risk
Risk reduction
Statistical analysis
Taiwan - epidemiology
title Functional dyspepsia in depression: A population‐based cohort study
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