Department of Genetics, Evolution and Environment, Institute of Healthy Ageing, University College London, London, UK.
Institute of Health Informatics, University College London, London, UK.
Aging Cell. 2022 Apr;21(4):e13524. doi: 10.1111/acel.13524. Epub 2022 Mar 8.
Genetic, environmental, and pharmacological interventions into the aging process can confer resistance to multiple age-related diseases in laboratory animals, including rhesus monkeys. These findings imply that individual mechanisms of aging might contribute to the co-occurrence of age-related diseases in humans and could be targeted to prevent these conditions simultaneously. To address this question, we text mined 917,645 literature abstracts followed by manual curation and found strong, non-random associations between age-related diseases and aging mechanisms in humans, confirmed by gene set enrichment analysis of GWAS data. Integration of these associations with clinical data from 3.01 million patients showed that age-related diseases associated with each of five aging mechanisms were more likely than chance to be present together in patients. Genetic evidence revealed that innate and adaptive immunity, the intrinsic apoptotic signaling pathway and activity of the ERK1/2 pathway were associated with multiple aging mechanisms and diverse age-related diseases. Mechanisms of aging hence contribute both together and individually to age-related disease co-occurrence in humans and could potentially be targeted accordingly to prevent multimorbidity.
遗传、环境和药理学干预衰老过程可以使实验动物(包括恒河猴)对多种与年龄相关的疾病产生抗性。这些发现表明,衰老的个体机制可能导致人类多种与年龄相关的疾病同时发生,并可针对这些情况同时进行预防。为了解决这个问题,我们对 917,645 篇文献摘要进行了文本挖掘,然后进行了人工编辑,发现人类与年龄相关的疾病和衰老机制之间存在很强的、非随机的关联,这一关联通过对 GWAS 数据的基因集富集分析得到了证实。将这些关联与来自 301 万患者的临床数据进行整合表明,与五种衰老机制中的每一种相关的与年龄相关的疾病比偶然同时出现在患者中的可能性更大。遗传证据表明,固有和适应性免疫、内在凋亡信号通路以及 ERK1/2 通路的活性与多种衰老机制和多种与年龄相关的疾病有关。因此,衰老机制共同和单独导致了人类多种与年龄相关的疾病的同时发生,并可能相应地成为预防多种疾病的目标。