Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA 02111, USA; Department of Medicine, School of Medicine, Tufts University, Boston, MA 02111, USA.
Department of Medicine, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, USA; Bioinformatics Program, Boston University, Boston, MA 02215, USA.
Cell Rep. 2024 Nov 26;43(11):114913. doi: 10.1016/j.celrep.2024.114913. Epub 2024 Nov 5.
Metabolites that mark aging are not fully known. We analyze 408 plasma metabolites in Long Life Family Study participants to characterize markers of age, aging, extreme longevity, and mortality. We identify 308 metabolites associated with age, 258 metabolites that change over time, 230 metabolites associated with extreme longevity, and 152 metabolites associated with mortality risk. We replicate many associations in independent studies. By summarizing the results into 19 signatures, we differentiate between metabolites that may mark aging-associated compensatory mechanisms from metabolites that mark cumulative damage of aging and from metabolites that characterize extreme longevity. We generate and validate a metabolomic clock that predicts biological age. Network analysis of the age-associated metabolites reveals a critical role of essential fatty acids to connect lipids with other metabolic processes. These results characterize many metabolites involved in aging and point to nutrition as a source of intervention for healthy aging therapeutics.
衰老的标志物尚未完全明确。我们分析了长寿家族研究参与者的 408 种血浆代谢物,以表征年龄、衰老、极端长寿和死亡率的标志物。我们确定了 308 种与年龄相关的代谢物、258 种随时间变化的代谢物、230 种与极端长寿相关的代谢物和 152 种与死亡风险相关的代谢物。我们在独立研究中复制了许多关联。通过将结果总结为 19 个特征,我们区分了可能标志与衰老相关的代偿机制的代谢物、标志衰老累积损伤的代谢物以及标志极端长寿的代谢物。我们生成并验证了一种可以预测生物年龄的代谢组钟。与年龄相关的代谢物的网络分析揭示了必需脂肪酸在将脂质与其他代谢过程联系起来方面的关键作用。这些结果描述了许多与衰老有关的代谢物,并指出营养是干预健康衰老治疗的一个来源。