Department of Psychiatry, University of California San Diego, La Jolla, CA 92093, USA.
Sam and Rose Stein Institute for Research on Aging, University of California San Diego, La Jolla, CA 92093, USA.
Nutrients. 2020 Dec 7;12(12):3759. doi: 10.3390/nu12123759.
Aging is determined by complex interactions among genetic and environmental factors. Increasing evidence suggests that the gut microbiome lies at the core of many age-associated changes, including immune system dysregulation and susceptibility to diseases. The gut microbiota undergoes extensive changes across the lifespan, and age-related processes may influence the gut microbiota and its related metabolic alterations. The aim of this systematic review was to summarize the current literature on aging-associated alterations in diversity, composition, and functional features of the gut microbiota. We identified 27 empirical human studies of normal and successful aging suitable for inclusion. Alpha diversity of microbial taxa, functional pathways, and metabolites was higher in older adults, particularly among the oldest-old adults, compared to younger individuals. Beta diversity distances significantly differed across various developmental stages and were different even between oldest-old and younger-old adults. Differences in taxonomic composition and functional potential varied across studies, but was most consistently reported to be relatively more abundant with aging, whereas , , and were relatively reduced. Older adults have reduced pathways related to carbohydrate metabolism and amino acid synthesis; however, oldest-old adults exhibited functional differences that distinguished their microbiota from that of young-old adults, such as greater potential for short-chain fatty acid production and increased butyrate derivatives. Although a definitive interpretation is limited by the cross-sectional design of published reports, we integrated findings of microbial composition and downstream functional pathways and metabolites, offering possible explanations regarding age-related processes.
衰老是由遗传和环境因素之间的复杂相互作用决定的。越来越多的证据表明,肠道微生物组是许多与年龄相关变化的核心,包括免疫系统失调和易患疾病。肠道微生物组在整个生命周期中经历广泛的变化,与年龄相关的过程可能会影响肠道微生物组及其相关的代谢改变。本系统综述的目的是总结目前关于肠道微生物组多样性、组成和功能特征与衰老相关变化的文献。我们确定了 27 项适合纳入的正常和成功衰老的人类实证研究。与年轻个体相比,老年人(尤其是最年长的老年人)的微生物类群、功能途径和代谢物的 alpha 多样性更高。β多样性距离在不同的发育阶段显著不同,即使在最年长的老年人和年轻老年人之间也存在差异。分类组成和功能潜力的差异因研究而异,但随着衰老,相对丰度增加的报道最为一致,而 、 和 则相对减少。老年人碳水化合物代谢和氨基酸合成相关的途径减少;然而,最年长的老年人表现出的功能差异使他们的微生物组与年轻老年人的微生物组区分开来,例如短链脂肪酸产生的潜力更大,丁酸盐衍生物增加。尽管由于已发表报告的横断面设计,对解释的明确性有限,但我们整合了微生物组成和下游功能途径和代谢物的发现,提供了与年龄相关过程相关的可能解释。