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Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency
OBJECTIVE: Epidemiological evidence indicated a relationship between vitamin D (VD) and depression with anxiety, but their therapeutic relationship has not been fully elucidated. This study aimed to examine whether VD supplementation would relieve symptoms in patients with depression and anxiety wit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667301/ https://www.ncbi.nlm.nih.gov/pubmed/32945627 http://dx.doi.org/10.1002/brb3.1760 |
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author | Zhu, Cuizhen Zhang, Yu Wang, Ting Lin, Yezhe Yu, Jiakuai Xia, Qingrong Zhu, Peng Zhu, Dao‐min |
author_facet | Zhu, Cuizhen Zhang, Yu Wang, Ting Lin, Yezhe Yu, Jiakuai Xia, Qingrong Zhu, Peng Zhu, Dao‐min |
author_sort | Zhu, Cuizhen |
collection | PubMed |
description | OBJECTIVE: Epidemiological evidence indicated a relationship between vitamin D (VD) and depression with anxiety, but their therapeutic relationship has not been fully elucidated. This study aimed to examine whether VD supplementation would relieve symptoms in patients with depression and anxiety with low serum 25‐hydroxy VD [25(OH) D] levels. METHOD: Participants with low 25(OH)D levels were randomized to control or daily VD group and were followed up for 6 months. Serum concentrations of 25(OH) D were measured using commercial kits. Psychological symptoms were evaluated with the Hamilton Depression Rating Scale‐17 (HAMD‐17), Revised Social Anhedonia Scale (RSAS), Revised Physical Anhedonia scale (RPAS), and Hamilton Anxiety Rating Scale‐14 (HAMA‐14). The trial was listed in the trial registration (http://www.medresman.org.cn/uc/index.aspx; NTR number: ChiCTR2000030130). RESULTS: In this clinical population, no significant difference in depression symptoms was detected between VD group and control group at both baseline and at the endpoint of our study. The HAMD‐17, RSAS, and RPAS scores did not change significantly between VD and control groups from baseline to endpoint (all p > .05). However, there was a significant difference in time effect of the total HAMA‐14 scores between the two groups (β [95% Cl] = −2.235 [−3.818, −0.653], p = .006). CONCLUSIONS: Vitamin D supplementation could improve the anxiety symptoms but not depressive symptoms in depressive patients with low VD level after the 6‐month intervention. |
format | Online Article Text |
id | pubmed-7667301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76673012020-11-20 Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency Zhu, Cuizhen Zhang, Yu Wang, Ting Lin, Yezhe Yu, Jiakuai Xia, Qingrong Zhu, Peng Zhu, Dao‐min Brain Behav Original Research OBJECTIVE: Epidemiological evidence indicated a relationship between vitamin D (VD) and depression with anxiety, but their therapeutic relationship has not been fully elucidated. This study aimed to examine whether VD supplementation would relieve symptoms in patients with depression and anxiety with low serum 25‐hydroxy VD [25(OH) D] levels. METHOD: Participants with low 25(OH)D levels were randomized to control or daily VD group and were followed up for 6 months. Serum concentrations of 25(OH) D were measured using commercial kits. Psychological symptoms were evaluated with the Hamilton Depression Rating Scale‐17 (HAMD‐17), Revised Social Anhedonia Scale (RSAS), Revised Physical Anhedonia scale (RPAS), and Hamilton Anxiety Rating Scale‐14 (HAMA‐14). The trial was listed in the trial registration (http://www.medresman.org.cn/uc/index.aspx; NTR number: ChiCTR2000030130). RESULTS: In this clinical population, no significant difference in depression symptoms was detected between VD group and control group at both baseline and at the endpoint of our study. The HAMD‐17, RSAS, and RPAS scores did not change significantly between VD and control groups from baseline to endpoint (all p > .05). However, there was a significant difference in time effect of the total HAMA‐14 scores between the two groups (β [95% Cl] = −2.235 [−3.818, −0.653], p = .006). CONCLUSIONS: Vitamin D supplementation could improve the anxiety symptoms but not depressive symptoms in depressive patients with low VD level after the 6‐month intervention. John Wiley and Sons Inc. 2020-09-18 /pmc/articles/PMC7667301/ /pubmed/32945627 http://dx.doi.org/10.1002/brb3.1760 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Zhu, Cuizhen Zhang, Yu Wang, Ting Lin, Yezhe Yu, Jiakuai Xia, Qingrong Zhu, Peng Zhu, Dao‐min Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency |
title | Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency |
title_full | Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency |
title_fullStr | Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency |
title_full_unstemmed | Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency |
title_short | Vitamin D supplementation improves anxiety but not depression symptoms in patients with vitamin D deficiency |
title_sort | vitamin d supplementation improves anxiety but not depression symptoms in patients with vitamin d deficiency |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667301/ https://www.ncbi.nlm.nih.gov/pubmed/32945627 http://dx.doi.org/10.1002/brb3.1760 |
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