血清Klotho与中年和老年美国人口中加速衰老之间的U形关联:一个横截面研究
Heng Li1,2, Shuai Miao3,4, Min Zhang1,2
1Department of Neurology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, 250014, People's Republic of China.
BMC geriatrics
|November 29, 2023
概括
血清Klotho表现出与加速衰老的U形关联. 较低的Klotho水平与衰老加速的减少相关,而较高的水平与中年和老年人的衰老加速的增加相关.
科学领域:
- 老年学是一门学科.
- 生物标志物 生物标志物
- 衰老研究研究 衰老研究
背景情况:
- 现型年龄加速通过比较现型年龄和时间年龄来衡量衰老速度.
- 克洛托蛋白与缓慢衰老有关,但其在加速衰老中的作用尚不清楚.
研究的目的:
- 研究血清Klotho水平与表型衰老加速之间的关联.
- 探索Klotho对衰老加速的潜在非线性关系和值效应.
主要方法:
- 利用了2007-2010年国家健康和营养检查调查的数据.
- 计算了4388名参与者 (40-79岁) 的表型年龄,使用了年代年龄和9个衰老生物标志物.
- 使用多变量线性回归,平滑曲线拟合和细分回归来分析血清Klotho与表型年龄加速之间的关联.
主要成果:
- 在血清Klotho和表型年龄加速之间观察到显著的U形关联 (p < 0.001).
- 随着血清Klotho低于870.7 pg/ml (β = -1.77) 的增加,表型年龄加速减少.
- 随着血清Klotho在870.7 pg/ml或以上的增加,表型年龄加速增加 (β = 1.03).
结论:
- 血清Klotho表明U形关系与加快的老龄化中年和老年美国人口.
- 这些发现表明,克洛托在衰老过程中扮演着复杂的角色,这对了解衰老加速有重要意义.
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