Yao Shanshan, Marron Megan M, Tian Qu, Watts Eleanor L, Clish Clary B, Shah Ravi V, Murthy Venkatesh L, Newman Anne B
University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
National Institute of Aging, Baltimore, Maryland, USA.
J Gerontol A Biol Sci Med Sci. 2025 May 5;80(6). doi: 10.1093/gerona/glaf057.
Metabolic-inflammatory states are central to multiorgan mechanisms of aging, but precise functional biomarkers of physiological aging remain less clear.
In the Health, Aging, and Body Composition study, we defined metabolomic profiles of the Healthy Aging Index (HAI), a composite of cardiovascular, lung, cognitive, metabolic, and renal function (0-10, with higher scores indicating poorer health) in a split set design from 2015 older participants (mean age 73.6 years; 50% women; 35% Black). We used standard regression to identify metabolomic correlates of Year 1 and Year 10 HAI, change in HAI over time, and mortality. A metabolite score of HAI was developed using LASSO regression.
We identified 42 metabolites consistently associated with Year 1 and Year 10 HAI, as well as change in HAI: 13 lipids, 4 amino acids, and 4 metabolites of other classes were associated with worse and worsening HAI while 20 lipids and 1 amino acid was associated with better and improving HAI. Most of these associations were no longer significant after additionally adjusting for inflammation biomarkers. A higher metabolite score of Year 1 HAI was associated with greater HAI deterioration over time (hold-out "test" set beta 0.40 [0.15-0.65]) and higher mortality (hold-out "test" set hazard ratio: 1.43 [1.23-1.67]).
A multiorgan healthy aging phenotype was linked to lipid metabolites, suggesting potential pathways related to mitochondrial function, oxidative stress, and inflammation. Metabolomics of HAI at older age were related to worsening health and mortality, suggesting potential links between metabolism and accelerated physiological aging.
代谢炎症状态是衰老多器官机制的核心,但生理衰老的精确功能生物标志物仍不太明确。
在健康、衰老和身体成分研究中,我们在一个分割集设计中,从2015名老年参与者(平均年龄73.6岁;50%为女性;35%为黑人)中定义了健康衰老指数(HAI)的代谢组学特征,HAI是心血管、肺、认知、代谢和肾功能的综合指标(0至10分,分数越高表明健康状况越差)。我们使用标准回归来确定第1年和第10年HAI的代谢组学相关性、HAI随时间的变化以及死亡率。使用套索回归开发了HAI的代谢物评分。
我们确定了42种代谢物与第1年和第10年的HAI以及HAI的变化始终相关:13种脂质、4种氨基酸和4种其他类别的代谢物与较差和恶化的HAI相关,而20种脂质和1种氨基酸与较好和改善的HAI相关。在额外调整炎症生物标志物后,这些关联大多不再显著。第1年HAI的代谢物评分越高,随时间HAI恶化程度越大(留出“测试”集β为0.40 [0.15 - 0.65]),死亡率越高(留出“测试”集风险比:1.43 [1.23 - 1.67])。
多器官健康衰老表型与脂质代谢物相关,提示与线粒体功能、氧化应激和炎症相关的潜在途径。老年时HAI的代谢组学与健康恶化和死亡率相关,提示代谢与加速生理衰老之间的潜在联系。