加快的生物衰老,遗传倾向,以及发生的膜心脏病
Yong-Jian Zhu1, Xiang-Ying Suo2, Jing Guo3
1Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
JACC. Asia
|August 16, 2025
概括
先进的生物衰老,通过克莱梅拉-杜巴尔方法测量生物年龄 (KDM-BA) 和PhenoAge加速,显著增加了膜心脏病 (VHD) 的风险. 这一发现强调了生物年龄作为VHD预测和干预的潜在目标.
科学领域:
- 心血管医学 心血管医学
- 衰老研究研究 衰老研究
- 遗传学 是一个遗传学.
背景情况:
- 生物衰老和心脏膜疾病 (VHD) 之间的关系仍未得到充分研究.
- 了解这种关联对于开发新的预防和治疗策略至关重要.
研究的目的:
- 调查两种生物年龄指标,克莱梅拉-杜巴尔方法生物年龄 (KDM-BA) 加速和PhenOAge 加速之间的关联,以及发生VHD的风险.
- 探索影响VHD风险的潜在基因环境相互作用.
主要方法:
- 分析了341,460名英国生物库参与者,没有先前存在的VHD.
- 使用KDM-BA和PhenoAge加速指标评估生物年龄.
- 通过多基因风险评分 (PRS) 来量化遗传风险,并评估与Cox模型的相互作用.
主要成果:
- 通过KDM-BA和PhenoAge加速表示的较老的生物年龄与VHD风险增加有显著的关联.
- 每一次KDM-BA加速的1-SD增加对应于35%更高的VHD风险 (HR:1.35).
- 与最低四分位数相比,KDM-BA加速的最高四分位数中的个体面临86%的VHD风险增加.
结论:
- 先进的生物衰老是心脏膜疾病的重要危险因素.
- 生物衰老加速为临床VHD风险预测和治疗干预提供了一个有希望的目标.
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