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Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants
Theory predicts that biological processes of aging may contribute to poor mental health in late life. To test this hypothesis, we evaluated prospective associations between biological age and incident depression and anxiety in 424,299 UK Biobank participants. We measured biological age from clinical...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119095/ https://www.ncbi.nlm.nih.gov/pubmed/37080981 http://dx.doi.org/10.1038/s41467-023-38013-7 |
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author | Gao, Xu Geng, Tong Jiang, Meijie Huang, Ninghao Zheng, Yinan Belsky, Daniel W. Huang, Tao |
author_facet | Gao, Xu Geng, Tong Jiang, Meijie Huang, Ninghao Zheng, Yinan Belsky, Daniel W. Huang, Tao |
author_sort | Gao, Xu |
collection | PubMed |
description | Theory predicts that biological processes of aging may contribute to poor mental health in late life. To test this hypothesis, we evaluated prospective associations between biological age and incident depression and anxiety in 424,299 UK Biobank participants. We measured biological age from clinical traits using the KDM-BA and PhenoAge algorithms. At baseline, participants who were biologically older more often experienced depression/anxiety. During a median of 8.7 years of follow-up, participants with older biological age were at increased risk of incident depression/anxiety (5.9% increase per standard deviation [SD] of KDM-BA acceleration, 95% confidence intervals [CI]: 3.3%–8.5%; 11.3% increase per SD of PhenoAge acceleration, 95% CI: 9.%–13.0%). Biological-aging-associated risk of depression/anxiety was independent of and additive to genetic risk measured by genome-wide-association-study-based polygenic scores. Advanced biological aging may represent a potential risk factor for incident depression/anxiety in midlife and older adults and a potential target for risk assessment and intervention. |
format | Online Article Text |
id | pubmed-10119095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101190952023-04-22 Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants Gao, Xu Geng, Tong Jiang, Meijie Huang, Ninghao Zheng, Yinan Belsky, Daniel W. Huang, Tao Nat Commun Article Theory predicts that biological processes of aging may contribute to poor mental health in late life. To test this hypothesis, we evaluated prospective associations between biological age and incident depression and anxiety in 424,299 UK Biobank participants. We measured biological age from clinical traits using the KDM-BA and PhenoAge algorithms. At baseline, participants who were biologically older more often experienced depression/anxiety. During a median of 8.7 years of follow-up, participants with older biological age were at increased risk of incident depression/anxiety (5.9% increase per standard deviation [SD] of KDM-BA acceleration, 95% confidence intervals [CI]: 3.3%–8.5%; 11.3% increase per SD of PhenoAge acceleration, 95% CI: 9.%–13.0%). Biological-aging-associated risk of depression/anxiety was independent of and additive to genetic risk measured by genome-wide-association-study-based polygenic scores. Advanced biological aging may represent a potential risk factor for incident depression/anxiety in midlife and older adults and a potential target for risk assessment and intervention. Nature Publishing Group UK 2023-04-20 /pmc/articles/PMC10119095/ /pubmed/37080981 http://dx.doi.org/10.1038/s41467-023-38013-7 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gao, Xu Geng, Tong Jiang, Meijie Huang, Ninghao Zheng, Yinan Belsky, Daniel W. Huang, Tao Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants |
title | Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants |
title_full | Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants |
title_fullStr | Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants |
title_full_unstemmed | Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants |
title_short | Accelerated biological aging and risk of depression and anxiety: evidence from 424,299 UK Biobank participants |
title_sort | accelerated biological aging and risk of depression and anxiety: evidence from 424,299 uk biobank participants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119095/ https://www.ncbi.nlm.nih.gov/pubmed/37080981 http://dx.doi.org/10.1038/s41467-023-38013-7 |
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