Jackson Matthew A, Jeffery Ian B, Beaumont Michelle, Bell Jordana T, Clark Andrew G, Ley Ruth E, O'Toole Paul W, Spector Tim D, Steves Claire J
School of Microbiology and Alimentary Pharmabiotic Centre, University College Cork, Cork, Ireland.
Department of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital Campus, 3rd & 4th Floor South Wing Block D, Westminster Bridge Road, London, SE1 7EH, UK.
Genome Med. 2016 Jan 29;8(1):8. doi: 10.1186/s13073-016-0262-7.
Frailty is arguably the biggest problem associated with population ageing, and associates with gut microbiome composition in elderly and care-dependent individuals. Here we characterize frailty associations with the gut microbiota in a younger community dwelling population, to identify targets for intervention to encourage healthy ageing.
We analysed 16S rRNA gene sequence data derived from faecal samples obtained from 728 female twins. Frailty was quantified using a frailty index (FI). Mixed effects models were used to identify associations with diversity, operational taxonomic units (OTUs) and taxa. OTU associations were replicated in the Eldermet cohort. Phenotypes were correlated with modules of OTUs collapsed by co-occurrence.
Frailty negatively associated with alpha diversity of the gut microbiota. Models considering a number of covariates identified 637 OTUs associated with FI. Twenty-two OTU associations were significant independent of alpha diversity. Species more abundant with frailty included Eubacterium dolichum and Eggerthella lenta. A Faecalibacterium prausnitzii OTU was less abundant in frailer individuals, and retained significance in discordant twin analysis. Sixty OTU associations were replicated in the Eldermet cohort. OTU co-occurrence modules had mutually exclusive associations between frailty and alpha diversity.
There was a striking negative association between frailty and gut microbiota diversity, underpinned by specific taxonomic associations. Whether these relationships are causal or consequential is unknown. Nevertheless, they represent targets for diagnostic surveillance, or for intervention studies to improve vitality in ageing.
衰弱可以说是与人口老龄化相关的最大问题,并且与老年人及需要护理者的肠道微生物群组成有关。在此,我们描述了年轻的社区居住人群中衰弱与肠道微生物群的关联,以确定促进健康老龄化的干预靶点。
我们分析了从728名女性双胞胎的粪便样本中获得的16S rRNA基因序列数据。使用衰弱指数(FI)对衰弱进行量化。采用混合效应模型来确定与多样性、操作分类单元(OTU)和分类群的关联。OTU关联在Eldermet队列中进行了重复验证。将表型与通过共现聚类的OTU模块进行相关性分析。
衰弱与肠道微生物群的α多样性呈负相关。考虑多个协变量的模型确定了637个与FI相关的OTU。22个OTU关联独立于α多样性具有显著性。与衰弱相关的丰度较高的物种包括长真杆菌和迟缓埃格特菌。在衰弱个体中,普拉梭菌OTU的丰度较低,并且在不一致双胞胎分析中仍具有显著性。60个OTU关联在Eldermet队列中得到了重复验证。OTU共现模块在衰弱和α多样性之间具有相互排斥的关联。
衰弱与肠道微生物群多样性之间存在显著的负相关,这由特定的分类学关联所支撑。这些关系是因果关系还是结果尚不清楚。然而,它们代表了诊断监测的靶点,或用于改善衰老活力的干预研究的靶点。