{"title":"绝经后的年数及其代谢组学特征与中年妇女的生物学衰老:一项基于人群的研究。","authors":"Bo Xie, Meiling Li, Qi Wang, Chunying Fu, Xiaoyi Wang, Dongshan Zhu","doi":"10.1038/s41514-025-00249-6","DOIUrl":null,"url":null,"abstract":"<p><p>This study analyzed UK Biobank data from 46,463 postmenopausal women to investigate metabolic changes linked to years since menopause (YSM) and their impact on aging biomarkers. Elastic net regression identified 115 YSM-associated metabolites, forming a metabolic signature strongly correlated with YSM (r = 0.30, P < 0.001). Each standard deviation increase in this metabolic signature was associated with decreased odds of long telomere length (0.94, 0.92-0.96), increased odds of high allostatic load (1.53, 1.50-1.56) and high PhenoAge (2.30, 2.17-2.44). Mediation analysis indicated that the metabolic signature explained 43.5% of the association between YSM and allostatic load, 9.09% between YSM and telomere length, and 89.3% between YSM and PhenoAge. These findings reveal how menopause-related metabolic shifts drive biological aging, highlighting potential intervention targets for postmenopausal health.</p>","PeriodicalId":94160,"journal":{"name":"npj aging","volume":"11 1","pages":"58"},"PeriodicalIF":4.1000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12216968/pdf/","citationCount":"0","resultStr":"{\"title\":\"Years since menopause and its metabolomic signature with biological aging in women at midlife: a population-based study.\",\"authors\":\"Bo Xie, Meiling Li, Qi Wang, Chunying Fu, Xiaoyi Wang, Dongshan Zhu\",\"doi\":\"10.1038/s41514-025-00249-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This study analyzed UK Biobank data from 46,463 postmenopausal women to investigate metabolic changes linked to years since menopause (YSM) and their impact on aging biomarkers. Elastic net regression identified 115 YSM-associated metabolites, forming a metabolic signature strongly correlated with YSM (r = 0.30, P < 0.001). Each standard deviation increase in this metabolic signature was associated with decreased odds of long telomere length (0.94, 0.92-0.96), increased odds of high allostatic load (1.53, 1.50-1.56) and high PhenoAge (2.30, 2.17-2.44). Mediation analysis indicated that the metabolic signature explained 43.5% of the association between YSM and allostatic load, 9.09% between YSM and telomere length, and 89.3% between YSM and PhenoAge. These findings reveal how menopause-related metabolic shifts drive biological aging, highlighting potential intervention targets for postmenopausal health.</p>\",\"PeriodicalId\":94160,\"journal\":{\"name\":\"npj aging\",\"volume\":\"11 1\",\"pages\":\"58\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12216968/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"npj aging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1038/s41514-025-00249-6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GERIATRICS & GERONTOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj aging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s41514-025-00249-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
本研究分析了英国生物银行46,463名绝经后妇女的数据,以调查绝经后年龄(YSM)相关的代谢变化及其对衰老生物标志物的影响。弹性网回归鉴定出115种YSM相关代谢物,形成了与YSM强相关的代谢特征(r = 0.30, P
Years since menopause and its metabolomic signature with biological aging in women at midlife: a population-based study.
This study analyzed UK Biobank data from 46,463 postmenopausal women to investigate metabolic changes linked to years since menopause (YSM) and their impact on aging biomarkers. Elastic net regression identified 115 YSM-associated metabolites, forming a metabolic signature strongly correlated with YSM (r = 0.30, P < 0.001). Each standard deviation increase in this metabolic signature was associated with decreased odds of long telomere length (0.94, 0.92-0.96), increased odds of high allostatic load (1.53, 1.50-1.56) and high PhenoAge (2.30, 2.17-2.44). Mediation analysis indicated that the metabolic signature explained 43.5% of the association between YSM and allostatic load, 9.09% between YSM and telomere length, and 89.3% between YSM and PhenoAge. These findings reveal how menopause-related metabolic shifts drive biological aging, highlighting potential intervention targets for postmenopausal health.