不同地点击:通过代谢学,蛋白质学和基因学阐明人类衰老中的性变异
Sihao Xiao1,2,3, Pallavi Kaushik1, Gaoyu Du4
1Nuffield Department of Population Health, University of Oxford, Oxford, UK.
medRxiv : the preprint server for health sciences
|November 24, 2025
概括
这项研究创建了一个特定于性别的代谢衰老时钟,揭示了男性和女性不同的衰老机制. 了解这些差异对于个性化的健康策略和公共卫生政策至关重要.
科学领域:
- 老年学是一门学科.
- 代谢学 代谢学 代谢学
- 遗传学 是一个遗传学.
背景情况:
- 老化的时钟经常忽视性别特异性差异.
- 代谢衰老机制在男性和女性之间有所不同.
研究的目的:
- 开发一个特定于性别的代谢衰老时钟.
- 在两性中确定加速或减缓代谢衰老的机制.
- 研究加速代谢年龄与健康结果之间的联系.
主要方法:
- 利用了来自390,941个人的英国生物库数据.
- 综合遗传,蛋白质组和流行病学数据.
- 开发了一种特定于性别的代谢衰老时钟.
主要成果:
- 确定了常见的和特定于性别的代谢衰老机制.
- 胆固醇,免疫和细胞过程的调节失调加速了衰老.
- 氧化应激,弹性和组织完整性减缓了衰老.
- 诸如生育平价和分娩年龄等生殖因素显示出保护作用.
- 加快的代谢年龄预测了发病率和死亡率,男性的相关性更强.
- 肥胖对代谢衰老和疾病风险的性别影响不同.
- 加快的代谢衰老预测男性的癌症,但不是女性.
结论:
- 代谢衰老过程表现出显著的性别差异.
- 性别特定的衰老时钟对于了解疾病易感性至关重要.
- 调查结果强调需要基于性别的医疗保健策略和公共卫生政策.
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