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Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review

BACKGROUND: Although post-stroke depression (PSD) affects one-third of patients following an acute stroke, pooled evidence addressing the correlation between a low vitamin D status and the risk of PSD remains inconclusive. METHODS: Comprehensive database search of Medline, EMBASE, Cochrane library,...

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Autores principales: Hung, Kuo-Chuan, Wu, Jheng-Yan, Illias, Amina M., Chiu, Chong-Chi, Chang, Ying-Jen, Liao, Shu-Wei, Wang, Kuei-Fen, Chen, I-Wen, Sun, Cheuk-Kwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983120/
https://www.ncbi.nlm.nih.gov/pubmed/36875853
http://dx.doi.org/10.3389/fnut.2023.1142035
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author Hung, Kuo-Chuan
Wu, Jheng-Yan
Illias, Amina M.
Chiu, Chong-Chi
Chang, Ying-Jen
Liao, Shu-Wei
Wang, Kuei-Fen
Chen, I-Wen
Sun, Cheuk-Kwan
author_facet Hung, Kuo-Chuan
Wu, Jheng-Yan
Illias, Amina M.
Chiu, Chong-Chi
Chang, Ying-Jen
Liao, Shu-Wei
Wang, Kuei-Fen
Chen, I-Wen
Sun, Cheuk-Kwan
author_sort Hung, Kuo-Chuan
collection PubMed
description BACKGROUND: Although post-stroke depression (PSD) affects one-third of patients following an acute stroke, pooled evidence addressing the correlation between a low vitamin D status and the risk of PSD remains inconclusive. METHODS: Comprehensive database search of Medline, EMBASE, Cochrane library, and Google Scholar was performed from inception to December 2022. The primary outcome was the association of PSD risk with a low vitamin D status, while the secondary outcomes included the relationship between PSD and other risk factors. RESULTS: Analysis of seven observational studies published between 2014 and 2022 with 1,580 patients showed pooled incidences of vitamin D deficiency (defined as 25[OH] D levels < 50 nmol/L) and PSD of 60.1 and 26.1%, respectively. Patients with PSD had a lower circulating vitamin D concentration compared to those without [mean difference (MD) =−13.94 nmol/L, 95% CI: −21.83 to −6.05, p = 0.0005, I(2) = 91%, six studies, 1,414 patients]. Meta-analysis also demonstrated a correlation between a low vitamin D level and an increased PSD risk [odd ratio (OR) = 3.25, 95% CI: 1.57–6.69, p = 0.001, I(2) = 78.7%, 1,108 patients], the heterogeneity of which was found to be associated with the incidence of vitamin D deficiency but not female proportion on meta-regression. Besides, female gender (OR = 1.78, 95% CI: 1.3–2.44, p = 0.003, I(2) = 31%, five studies, 1,220 patients), hyperlipidemia (OR = 1.55, 95% CI: 1.01–2.36, p = 0.04, I(2) = 0%, four studies, 976 patients), and high National Institutes of Health Stroke Scale (NIHSS) scores (MD = 1.45, 95% CI: 0.58–2.32, p = 0.001, I(2) = 82%, five studies, 1,220 patients) were potential risk factors for PSD. For the primary outcome, the certainty of evidence was very low. Regarding secondary outcomes, the certainty of evidence was low for BMI, female gender, hypertension, diabetes, and stroke history, and very low for age, level of education, hyperlipidemia, cardiovascular disease, and NIHSS scores. CONCLUSION: The results suggested an association of a low circulating vitamin D level with an increased risk of PSD. Besides, female gender, hyperlipidemia, high NIHSS score were related to an increased risk or occurrence of PSD. The current study may imply the necessity of routine circulating vitamin D screening in this population. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/, identifier CRD42022381580.
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spelling pubmed-99831202023-03-04 Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review Hung, Kuo-Chuan Wu, Jheng-Yan Illias, Amina M. Chiu, Chong-Chi Chang, Ying-Jen Liao, Shu-Wei Wang, Kuei-Fen Chen, I-Wen Sun, Cheuk-Kwan Front Nutr Nutrition BACKGROUND: Although post-stroke depression (PSD) affects one-third of patients following an acute stroke, pooled evidence addressing the correlation between a low vitamin D status and the risk of PSD remains inconclusive. METHODS: Comprehensive database search of Medline, EMBASE, Cochrane library, and Google Scholar was performed from inception to December 2022. The primary outcome was the association of PSD risk with a low vitamin D status, while the secondary outcomes included the relationship between PSD and other risk factors. RESULTS: Analysis of seven observational studies published between 2014 and 2022 with 1,580 patients showed pooled incidences of vitamin D deficiency (defined as 25[OH] D levels < 50 nmol/L) and PSD of 60.1 and 26.1%, respectively. Patients with PSD had a lower circulating vitamin D concentration compared to those without [mean difference (MD) =−13.94 nmol/L, 95% CI: −21.83 to −6.05, p = 0.0005, I(2) = 91%, six studies, 1,414 patients]. Meta-analysis also demonstrated a correlation between a low vitamin D level and an increased PSD risk [odd ratio (OR) = 3.25, 95% CI: 1.57–6.69, p = 0.001, I(2) = 78.7%, 1,108 patients], the heterogeneity of which was found to be associated with the incidence of vitamin D deficiency but not female proportion on meta-regression. Besides, female gender (OR = 1.78, 95% CI: 1.3–2.44, p = 0.003, I(2) = 31%, five studies, 1,220 patients), hyperlipidemia (OR = 1.55, 95% CI: 1.01–2.36, p = 0.04, I(2) = 0%, four studies, 976 patients), and high National Institutes of Health Stroke Scale (NIHSS) scores (MD = 1.45, 95% CI: 0.58–2.32, p = 0.001, I(2) = 82%, five studies, 1,220 patients) were potential risk factors for PSD. For the primary outcome, the certainty of evidence was very low. Regarding secondary outcomes, the certainty of evidence was low for BMI, female gender, hypertension, diabetes, and stroke history, and very low for age, level of education, hyperlipidemia, cardiovascular disease, and NIHSS scores. CONCLUSION: The results suggested an association of a low circulating vitamin D level with an increased risk of PSD. Besides, female gender, hyperlipidemia, high NIHSS score were related to an increased risk or occurrence of PSD. The current study may imply the necessity of routine circulating vitamin D screening in this population. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/, identifier CRD42022381580. Frontiers Media S.A. 2023-02-16 /pmc/articles/PMC9983120/ /pubmed/36875853 http://dx.doi.org/10.3389/fnut.2023.1142035 Text en Copyright © 2023 Hung, Wu, Illias, Chiu, Chang, Liao, Wang, Chen and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Hung, Kuo-Chuan
Wu, Jheng-Yan
Illias, Amina M.
Chiu, Chong-Chi
Chang, Ying-Jen
Liao, Shu-Wei
Wang, Kuei-Fen
Chen, I-Wen
Sun, Cheuk-Kwan
Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review
title Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review
title_full Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review
title_fullStr Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review
title_full_unstemmed Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review
title_short Association of a low vitamin D status with risk of post-stroke depression: A meta-analysis and systematic review
title_sort association of a low vitamin d status with risk of post-stroke depression: a meta-analysis and systematic review
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983120/
https://www.ncbi.nlm.nih.gov/pubmed/36875853
http://dx.doi.org/10.3389/fnut.2023.1142035
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