Identifying potential drug targets for physical and cognitive frailty: an integrative analysis of CHARLS cohort, mendelian randomization, and gene colocalization.

IF 5.3 4区 医学 Q1 GERIATRICS & GERONTOLOGY
Wen Liu, Jie Zhao, Zeng-Qiang Liu, Xiao-di Sun, Yuan-Yuan Dong, Yu-Jie Meng, Wei-Dong Jiang, Zhen Liu
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引用次数: 0

Abstract

With the aging of the population, frailty has become a common syndrome that severely affects the quality of life of older adults. This study aims to analyze the correlation between cognition and frailty, physical activity and frailty, and elucidate the potential pharmacological targets of cognitive frailty and physical frailty.We conducted logistic regression analyses using data from the China Health and Retirement Longitudinal Study (CHARLS) to examine the associations between total cognition and frailty, physical activity and frailty. Furthermore, summary-data-based Mendelian randomization (SMR) and two-sample Mendelian randomization (TSMR) were employed to explore potential pharmacological targets for frailty. Genes associated with physical frailty and cognitive frailty were identified, followed by analysis via colocalization analysis, phenome-wide association studies (PheWAS), and DsigDB drug prediction. Cross-sectional analysis of CHARLs revealed that total cognition(OR 0.93, 95% CI 0.92-0.95) and middle physical activity(OR 0.95, 95% CI 0.92-0.97) were negatively correlated with frailty. SMR identified 41 drug genes associated with frailty, and subsequent TSMR validation and co-localization analysis showed that 11 candidate genes exhibited strong colocalization (PP.H4 > 0.8). GRPEL 1, PABPC 4, and WBP 2NL were ultimately identified as potential drug targets associated with physical frailty, while LANCL1, LRPPRC, FADS1, and WBP2NL were identified as potential drug targets associated with cognitive frailty. Phenome-wide association analysis(PheWAS) did not reveal any significant associations between these genes and other phenotypes at the genome-wide significance threshold. Laudanosine, 25-hydroxycholesterol, and hexadecanal emerged as the top three candidate compounds for therapeutic intervention. We identified potential drug targets for physical frailty and cognitive frailty through comprehensive analysis and elucidated drugs associated with potentially relevant genetic markers, thereby laying the foundation for a deeper understanding of the mechanisms of frailty.

识别身体和认知衰弱的潜在药物靶点:CHARLS队列、孟德尔随机化和基因共定位的综合分析。
随着人口的老龄化,身体虚弱已经成为严重影响老年人生活质量的一种常见症状。本研究旨在分析认知与虚弱、体力活动与虚弱的相关性,阐明认知虚弱和身体虚弱的潜在药理靶点。我们使用中国健康与退休纵向研究(CHARLS)的数据进行了逻辑回归分析,以检验总体认知与虚弱、身体活动与虚弱之间的关系。此外,采用基于汇总数据的孟德尔随机化(SMR)和双样本孟德尔随机化(TSMR)来探索潜在的脆性药理靶点。确定与身体虚弱和认知虚弱相关的基因,然后通过共定位分析、全现象关联研究(PheWAS)和DsigDB药物预测进行分析。charl的横断面分析显示,总体认知(OR 0.93, 95% CI 0.92-0.95)和中等体力活动(OR 0.95, 95% CI 0.92-0.97)与虚弱呈负相关。SMR鉴定出41个与脆性相关的药物基因,随后的TSMR验证和共定位分析显示,11个候选基因表现出强共定位(PP.H4 > 0.8)。GRPEL 1、PABPC 4和WBP2NL最终被确定为与身体虚弱相关的潜在药物靶点,而LANCL1、LRPPRC、FADS1和WBP2NL被确定为与认知虚弱相关的潜在药物靶点。全表型关联分析(PheWAS)在全基因组显著性阈值下未发现这些基因与其他表型之间存在显著关联。Laudanosine, 25-羟基胆固醇和hexadecanal成为治疗干预的前三个候选化合物。我们通过综合分析确定了身体虚弱和认知虚弱的潜在药物靶点,并阐明了与潜在相关遗传标记相关的药物,从而为更深入地了解虚弱的机制奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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