Nutrition, Exercise Physiology and Sarcopenia Laboratory, Jean Mayer USDA Human Nutrition Research Center On Aging, Tufts University, Boston, MA, USA.
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Geroscience. 2022 Dec;44(6):2757-2770. doi: 10.1007/s11357-022-00685-2. Epub 2022 Nov 11.
Cellular senescence is a plausible mediator of age-associated declines in physical performance. To test this premise, we examined cross-sectional associations between circulating components of the senescence-associated secretory phenotype (SASP) and measures of physical function and muscle strength in 1377 older adults. We showed significant associations between multiple SASP proteins and the short physical performance battery (SPPB), its subcomponents (gait speed, balance, chair rise time), and 400-m walk time. Activin A, ICAM1, MMP7, VEGFA, and eotaxin showed strong associations based on gradient boost machine learning (GBM), and, when combined with other proteins, effectively identified participants at the greatest risk for mobility disability (SPPB score [Formula: see text] 7). Senescence biomarkers were also associated with lower grip strength, and GBM identified PARC, ADAMTS13, and RANTES as top candidates in females, and MMP2, SOST, and MCP1 in males. These findings highlight an association between senescence biomarkers and physical performance in older adults. ClinicalTrials.gov Identifier: NCT01072500.
细胞衰老可能是与年龄相关的身体机能下降的中介。为了验证这一前提,我们在 1377 名老年人中研究了衰老相关分泌表型 (SASP) 的循环成分与身体机能和肌肉力量测量之间的横断面关联。我们发现多种 SASP 蛋白与短体机能测试 (SPPB)、其分量表 (步态速度、平衡、起坐时间) 和 400 米步行时间之间存在显著关联。基于梯度提升机 (GBM) 的学习,激活素 A、ICAM1、MMP7、VEGFA 和嗜酸性粒细胞趋化因子表现出强烈关联,当与其他蛋白结合时,可有效识别出最易发生移动障碍的参与者 (SPPB 评分[Formula: see text]7)。衰老生物标志物也与握力降低有关,GBM 确定 PARC、ADAMTS13 和 RANTES 是女性的最佳候选者,而 MMP2、SOST 和 MCP1 是男性的最佳候选者。这些发现突出了衰老生物标志物与老年人身体机能之间的关联。临床试验编号:NCT01072500。