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Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study

BACKGROUND: Patients with ankylosing spondylitis (AS) have a higher prevalence of depression compared to the general population. Comorbid depression in AS likely has a multifactorial origin. While several disease-related and contextual factors have been associated with depressive symptoms in AS, a c...

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Autores principales: Webers, Casper, Vanhoof, Laura, Leue, Carsten, Boonen, Annelies, Köhler, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805406/
https://www.ncbi.nlm.nih.gov/pubmed/31639012
http://dx.doi.org/10.1186/s13075-019-1995-7
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author Webers, Casper
Vanhoof, Laura
Leue, Carsten
Boonen, Annelies
Köhler, Sebastian
author_facet Webers, Casper
Vanhoof, Laura
Leue, Carsten
Boonen, Annelies
Köhler, Sebastian
author_sort Webers, Casper
collection PubMed
description BACKGROUND: Patients with ankylosing spondylitis (AS) have a higher prevalence of depression compared to the general population. Comorbid depression in AS likely has a multifactorial origin. While several disease-related and contextual factors have been associated with depressive symptoms in AS, a comprehensive model of their interrelations is currently lacking. Such a model could help understand the mechanisms leading to, or maintaining, depression in AS. The objectives of the current study were to determine which factors are associated with depressive symptoms in AS and to understand their underlying relationships. METHODS: Data from a cross-sectional survey-based multicentre study were used. Potential determinants included both contextual and disease-related factors. Depressive symptoms were assessed by the Hospital Anxiety and Depression Subscale (HADS-D). Direct and indirect associations between risk factors and the latent depressive symptom outcome were explored using structural equation modelling. A final model was selected based on model fit criteria and clinical plausibility. RESULTS: Among 245 patients, median HADS-D score was 3 (interquartile range 1–6), and 44 patients (18%) had a HADS-D score ≥ 8, indicating possible depression. In the final model, contextual factors significantly associated with depressive symptoms were male gender, being employed, lower income, lower mastery and worse satisfaction with social role participation. Bath AS Disease Activity Index (BASDAI) was the only disease-related factor that was associated with depressive symptoms, acted only indirectly via mastery, and its standardized total effect on depressive symptoms was smaller than that of several contextual factors. Mastery had a central role in the path diagram and mediated the effects of BASDAI, income and satisfaction with social role participation on depressive symptoms. The final model explained 64% of the variance in the depression outcome. CONCLUSIONS: Both contextual and disease-related factors are associated with depressive symptoms in AS. Mastery, the extent to which one feels in control over life and disease, has a key role in this process. Results support a relevance of self-efficacy in disease management and patient education. In order to improve patients’ mental health, research is warranted whether mastery and its relation with depression can be modified. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s13075-019-1995-7.
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spelling pubmed-68054062019-10-24 Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study Webers, Casper Vanhoof, Laura Leue, Carsten Boonen, Annelies Köhler, Sebastian Arthritis Res Ther Research Article BACKGROUND: Patients with ankylosing spondylitis (AS) have a higher prevalence of depression compared to the general population. Comorbid depression in AS likely has a multifactorial origin. While several disease-related and contextual factors have been associated with depressive symptoms in AS, a comprehensive model of their interrelations is currently lacking. Such a model could help understand the mechanisms leading to, or maintaining, depression in AS. The objectives of the current study were to determine which factors are associated with depressive symptoms in AS and to understand their underlying relationships. METHODS: Data from a cross-sectional survey-based multicentre study were used. Potential determinants included both contextual and disease-related factors. Depressive symptoms were assessed by the Hospital Anxiety and Depression Subscale (HADS-D). Direct and indirect associations between risk factors and the latent depressive symptom outcome were explored using structural equation modelling. A final model was selected based on model fit criteria and clinical plausibility. RESULTS: Among 245 patients, median HADS-D score was 3 (interquartile range 1–6), and 44 patients (18%) had a HADS-D score ≥ 8, indicating possible depression. In the final model, contextual factors significantly associated with depressive symptoms were male gender, being employed, lower income, lower mastery and worse satisfaction with social role participation. Bath AS Disease Activity Index (BASDAI) was the only disease-related factor that was associated with depressive symptoms, acted only indirectly via mastery, and its standardized total effect on depressive symptoms was smaller than that of several contextual factors. Mastery had a central role in the path diagram and mediated the effects of BASDAI, income and satisfaction with social role participation on depressive symptoms. The final model explained 64% of the variance in the depression outcome. CONCLUSIONS: Both contextual and disease-related factors are associated with depressive symptoms in AS. Mastery, the extent to which one feels in control over life and disease, has a key role in this process. Results support a relevance of self-efficacy in disease management and patient education. In order to improve patients’ mental health, research is warranted whether mastery and its relation with depression can be modified. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s13075-019-1995-7. BioMed Central 2019-10-21 2019 /pmc/articles/PMC6805406/ /pubmed/31639012 http://dx.doi.org/10.1186/s13075-019-1995-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Webers, Casper
Vanhoof, Laura
Leue, Carsten
Boonen, Annelies
Köhler, Sebastian
Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
title Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
title_full Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
title_fullStr Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
title_full_unstemmed Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
title_short Depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
title_sort depression in ankylosing spondylitis and the role of disease-related and contextual factors: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805406/
https://www.ncbi.nlm.nih.gov/pubmed/31639012
http://dx.doi.org/10.1186/s13075-019-1995-7
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