Valentin Max Vetter, Kamil Demircan, Jan Homann, Thilo Samson Chillon, Michael Mülleder, Orr Shomroni, Elisabeth Steinhagen-Thiessen, Markus Ralser, Christina M. Lill, Lars Bertram, Lutz Schomburg, Ilja Demuth
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引用次数: 0
摘要
导言 生物年龄反映了个体间在生物功能和能力方面的差异,而非计时年龄。生物年龄可通过 DNA 甲基化年龄(DNAmA)及其与生理年龄的偏差,即 DNAmA 加速(DNAmAA)来估算。血清硒、硒蛋白 P(SELENOP)和含硒半胱氨酸的谷胱甘肽过氧化物酶 3(GPx3)水平低与不良健康后果有关,因此补硒被视为一种抗衰老干预措施。
Low Blood Levels of Selenium, Selenoprotein P and GPx3 are Associated with Accelerated Biological Aging: Results from the Berlin Aging Study II (BASE-II)
Introduction Biological age reflects inter-individual differences in biological function and capacity beyond chronological age. Biological age can be estimated by DNA methylation age (DNAmA) and its deviation from chronological age, DNAmA acceleration (DNAmAA). Low levels of serum selenium, selenoprotein P (SELENOP), and the selenocysteine-containing glutathione peroxidase 3 (GPx3) are associated with adverse health outcomes and selenium supplementation is discussed as an anti-aging intervention.