{"title":"虚弱和年龄相关性黄斑变性的风险:一项前瞻性队列和孟德尔随机化研究","authors":"Xinyu Zhu, Yikeng Huang, Li Liang, Xinyu Zhang, Zixuan Zhang, Yujin Jiang, Xiaoqian Wu, Chenxin Li, Zhi Zheng, Zhangli Bao, Wenjun Zou, Shuzhi Zhao","doi":"10.1093/gerona/glae300","DOIUrl":null,"url":null,"abstract":"Background Both frailty and age-related macular degeneration (AMD) are related to aging and may share some common mechanisms. We aimed to examine the observational and causal association between frailty and the risk of age-related macular degeneration (AMD). Methods We included 320,810 participants free of AMD at baseline from the UK Biobank. Frailty phenotypes were defined according to 5 components: weight loss, exhaustion, slow gait speed, low grip strength, and low physical activity. Cox proportional hazard models were used to evaluate the association between frailty phenotype and the risk of AMD. Causal relationship between frailty phenotype and AMD was examined using two-sample Mendelian randomization (MR) analysis. Results During a median follow-up of 12.81 years, 7,222 AMD cases were documented. After adjusting for confounding factors, compared with non-frail participants, both pre-frail and frail participants were significantly associated with an increased risk of AMD (HR 1.17, 95% CI: [1.11, 1.23] for pre-frailty and HR 1.55 [95% CI: 1.40, 1.73] for frailty). With each one-point increase in frailty phenotype score, the risk of AMD increased by 14%. Results from the two-sample MR analysis supported the potential causal effect of frailty phenotype on AMD. Conclusions Our findings suggested that frailty assessment may help identify at-risk populations and serve as a potential strategy for early prevention and management of AMD.","PeriodicalId":22892,"journal":{"name":"The Journals of Gerontology Series A: Biological Sciences and Medical Sciences","volume":"280 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Frailty and the risk of age-related macular degeneration: a prospective cohort and Mendelian randomization study\",\"authors\":\"Xinyu Zhu, Yikeng Huang, Li Liang, Xinyu Zhang, Zixuan Zhang, Yujin Jiang, Xiaoqian Wu, Chenxin Li, Zhi Zheng, Zhangli Bao, Wenjun Zou, Shuzhi Zhao\",\"doi\":\"10.1093/gerona/glae300\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background Both frailty and age-related macular degeneration (AMD) are related to aging and may share some common mechanisms. We aimed to examine the observational and causal association between frailty and the risk of age-related macular degeneration (AMD). Methods We included 320,810 participants free of AMD at baseline from the UK Biobank. Frailty phenotypes were defined according to 5 components: weight loss, exhaustion, slow gait speed, low grip strength, and low physical activity. Cox proportional hazard models were used to evaluate the association between frailty phenotype and the risk of AMD. Causal relationship between frailty phenotype and AMD was examined using two-sample Mendelian randomization (MR) analysis. Results During a median follow-up of 12.81 years, 7,222 AMD cases were documented. After adjusting for confounding factors, compared with non-frail participants, both pre-frail and frail participants were significantly associated with an increased risk of AMD (HR 1.17, 95% CI: [1.11, 1.23] for pre-frailty and HR 1.55 [95% CI: 1.40, 1.73] for frailty). With each one-point increase in frailty phenotype score, the risk of AMD increased by 14%. Results from the two-sample MR analysis supported the potential causal effect of frailty phenotype on AMD. Conclusions Our findings suggested that frailty assessment may help identify at-risk populations and serve as a potential strategy for early prevention and management of AMD.\",\"PeriodicalId\":22892,\"journal\":{\"name\":\"The Journals of Gerontology Series A: Biological Sciences and Medical Sciences\",\"volume\":\"280 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journals of Gerontology Series A: Biological Sciences and Medical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/gerona/glae300\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journals of Gerontology Series A: Biological Sciences and Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/gerona/glae300","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Frailty and the risk of age-related macular degeneration: a prospective cohort and Mendelian randomization study
Background Both frailty and age-related macular degeneration (AMD) are related to aging and may share some common mechanisms. We aimed to examine the observational and causal association between frailty and the risk of age-related macular degeneration (AMD). Methods We included 320,810 participants free of AMD at baseline from the UK Biobank. Frailty phenotypes were defined according to 5 components: weight loss, exhaustion, slow gait speed, low grip strength, and low physical activity. Cox proportional hazard models were used to evaluate the association between frailty phenotype and the risk of AMD. Causal relationship between frailty phenotype and AMD was examined using two-sample Mendelian randomization (MR) analysis. Results During a median follow-up of 12.81 years, 7,222 AMD cases were documented. After adjusting for confounding factors, compared with non-frail participants, both pre-frail and frail participants were significantly associated with an increased risk of AMD (HR 1.17, 95% CI: [1.11, 1.23] for pre-frailty and HR 1.55 [95% CI: 1.40, 1.73] for frailty). With each one-point increase in frailty phenotype score, the risk of AMD increased by 14%. Results from the two-sample MR analysis supported the potential causal effect of frailty phenotype on AMD. Conclusions Our findings suggested that frailty assessment may help identify at-risk populations and serve as a potential strategy for early prevention and management of AMD.