Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.
Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, USA.
Aging Cell. 2024 Feb;23(2):e14038. doi: 10.1111/acel.14038. Epub 2023 Nov 14.
Calorie restriction (CR) with adequate nutrient intake is a potential geroprotective intervention. To advance this concept in humans, we tested the hypothesis that moderate CR in healthy young-to-middle-aged individuals would reduce circulating biomarkers of cellular senescence, a fundamental mechanism of aging and aging-related conditions. Using plasma specimens from the Comprehensive Assessment of Long-term Effects of Reducing Intake of Energy (CALERIE™) phase 2 study, we found that CR significantly reduced the concentrations of several senescence biomarkers at 12 and 24 months compared to an ad libitum diet. Using machine learning, changes in biomarker concentrations emerged as important predictors of the change in HOMA-IR and insulin sensitivity index at 12 and 24 months, and the change in resting metabolic rate residual at 12 months. Finally, using adipose tissue RNA-sequencing data from a subset of participants, we observed a significant reduction in a senescence-focused gene set in response to CR at both 12 and 24 months compared to baseline. Our results advance the understanding of the effects of CR in humans and further support a link between cellular senescence and metabolic health.
热量限制(CR)结合充足的营养摄入是一种潜在的抗衰老干预措施。为了在人类中推进这一概念,我们检验了这样一个假设,即健康的中青年人群适度的 CR 会降低循环细胞衰老生物标志物的浓度,细胞衰老是衰老和与衰老相关疾病的基本机制。利用来自能量摄入减少的长期综合评估(CALERIE™)第 2 阶段研究的血浆标本,我们发现与自由进食相比,CR 在 12 个月和 24 个月时显著降低了几种衰老生物标志物的浓度。使用机器学习,生物标志物浓度的变化成为 12 个月和 24 个月时 HOMA-IR 和胰岛素敏感指数变化以及 12 个月时静息代谢率残留变化的重要预测因素。最后,使用一部分参与者的脂肪组织 RNA 测序数据,我们观察到在 12 个月和 24 个月时,与基线相比,对 CR 的反应中一个以衰老为重点的基因集显著减少。我们的研究结果加深了对人类 CR 影响的理解,并进一步支持了细胞衰老与代谢健康之间的联系。