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Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study

OBJECTIVE: Rheumatoid arthritis (RA) is a costly and crippling autoimmune disease that can lead to the development of depression, contributing to suboptimal clinical outcomes. However, no longitudinal studies have identified an association between rheumatoid arthritis and subsequent depression. This...

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Autores principales: Lin, Miao-Chiu, Guo, How-Ran, Lu, Ming-Chi, Livneh, Hanoch, Lai, Ning-Sheng, Tsai, Tzung-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351304/
https://www.ncbi.nlm.nih.gov/pubmed/25789516
http://dx.doi.org/10.6061/clinics/2015(02)04
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author Lin, Miao-Chiu
Guo, How-Ran
Lu, Ming-Chi
Livneh, Hanoch
Lai, Ning-Sheng
Tsai, Tzung-Yi
author_facet Lin, Miao-Chiu
Guo, How-Ran
Lu, Ming-Chi
Livneh, Hanoch
Lai, Ning-Sheng
Tsai, Tzung-Yi
author_sort Lin, Miao-Chiu
collection PubMed
description OBJECTIVE: Rheumatoid arthritis (RA) is a costly and crippling autoimmune disease that can lead to the development of depression, contributing to suboptimal clinical outcomes. However, no longitudinal studies have identified an association between rheumatoid arthritis and subsequent depression. This study aimed to investigate the incidence and risk factors of depression among RA patients in Taiwan. METHODS: Using Taiwan's National Health Insurance Research Database, we identified 3,698 newly diagnosed RA patients aged 18 years or older, together with 7,396 subjects without RA matched by sex, age and index date, between 2000 and 2004. The incidence of depression and the risk factors among RA cases were evaluated using Cox proportional-hazard regression. RESULTS: The incidence of depression was 1.74-fold greater in the RA cohort than in the non-RA cohort (11.80 versus 6.89 per 1,000 person-years; p<0.01). Multivariate analysis showed that RA subjects who were female, were older, or had comorbidities such as stroke, chronic kidney disease, or cancer had a significantly greater risk of depression compared with those without these conditions. CONCLUSION: This population-based cohort study showed a strong relationship between RA and a subsequent risk of depression. The findings could be beneficial to healthcare providers for identifying individuals with a higher predisposition for depression, thereby possibly facilitating the provision of an appropriate rehabilitation intervention after RA onset to support the patient's adaptation.
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spelling pubmed-43513042015-03-16 Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study Lin, Miao-Chiu Guo, How-Ran Lu, Ming-Chi Livneh, Hanoch Lai, Ning-Sheng Tsai, Tzung-Yi Clinics (Sao Paulo) Clinical Science OBJECTIVE: Rheumatoid arthritis (RA) is a costly and crippling autoimmune disease that can lead to the development of depression, contributing to suboptimal clinical outcomes. However, no longitudinal studies have identified an association between rheumatoid arthritis and subsequent depression. This study aimed to investigate the incidence and risk factors of depression among RA patients in Taiwan. METHODS: Using Taiwan's National Health Insurance Research Database, we identified 3,698 newly diagnosed RA patients aged 18 years or older, together with 7,396 subjects without RA matched by sex, age and index date, between 2000 and 2004. The incidence of depression and the risk factors among RA cases were evaluated using Cox proportional-hazard regression. RESULTS: The incidence of depression was 1.74-fold greater in the RA cohort than in the non-RA cohort (11.80 versus 6.89 per 1,000 person-years; p<0.01). Multivariate analysis showed that RA subjects who were female, were older, or had comorbidities such as stroke, chronic kidney disease, or cancer had a significantly greater risk of depression compared with those without these conditions. CONCLUSION: This population-based cohort study showed a strong relationship between RA and a subsequent risk of depression. The findings could be beneficial to healthcare providers for identifying individuals with a higher predisposition for depression, thereby possibly facilitating the provision of an appropriate rehabilitation intervention after RA onset to support the patient's adaptation. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2015-02 /pmc/articles/PMC4351304/ /pubmed/25789516 http://dx.doi.org/10.6061/clinics/2015(02)04 Text en Copyright © 2015 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Lin, Miao-Chiu
Guo, How-Ran
Lu, Ming-Chi
Livneh, Hanoch
Lai, Ning-Sheng
Tsai, Tzung-Yi
Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
title Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
title_full Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
title_fullStr Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
title_full_unstemmed Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
title_short Increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
title_sort increased risk of depression in patients with rheumatoid arthritis: a seven-year population-based cohort study
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351304/
https://www.ncbi.nlm.nih.gov/pubmed/25789516
http://dx.doi.org/10.6061/clinics/2015(02)04
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