Frailty in Ageing Research Group, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium; Gerontology Department, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium; Department of Biochemistry and Molecular Biology, Faculty of Science, University of Buea, P.O Box 63, Buea, Cameroon.
Frailty in Ageing Research Group, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium; Gerontology Department, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium; Department of Geriatric Medicine, Universitair Ziekenhuis Brussel, Laarbeeklaan 101, B-1090 Brussels, Belgium.
Exp Gerontol. 2020 Nov;141:111079. doi: 10.1016/j.exger.2020.111079. Epub 2020 Aug 31.
Ageing is characterized by a low-grade chronic inflammation marked by elevated circulating levels of inflammatory mediators. This chronic inflammation occurring in the absence of obvious infection has been coined as inflammageing and represents a risk factor for morbidity and mortality in the geriatric population. Also, with ageing, important perturbations in the gut microbiota have been underlined and a growing body of literature has implicated age-related gut dysbiosis as contributing to a global inflammatory state in the elderly. Notwithstanding, very little attention has been given to how gut microbiota impact inflammageing. Here, we investigate the available evidence regarding the association between inflammageing and gut microbiota during ageing. PubMed, Web of Science and Scopus were systematically screened, and seven relevant articles in animals or humans were retrieved. The animal studies reported that Parabacteroides, Mucispirillum, Clostridium and Sarcina positively associate with the pro-inflammatory MCP-1 while Akkermansia, Oscillospira, Blautia and Lactobacillus negatively correlate with MCP-1. Furthermore, "aged"-type microbiota were associated with increased levels of IL6, IL-10, Th1, Th2, Treg, TNF-α, TGF-β, p16, SAMHD1, Eotaxin, and RANTES; activation of TLR2, NF-κB and mTOR; and with decreased levels of cyclin E and CDK2. On the other hand, the study on humans demonstrated that bacteria of the phylum Proteobacteria exhibited a positive correlation with IL-6 and IL-8, while Ruminococcus lactaris et rel. portrayed a negative correlation with IL-8. We conclude that changes in "aged"-type gut microbiota are associated with inflammageing.
衰老是一种以炎症介质循环水平升高为特征的低度慢性炎症。这种在没有明显感染的情况下发生的慢性炎症被称为炎症衰老,是老年人群发病率和死亡率的一个危险因素。此外,随着年龄的增长,肠道微生物群发生了重要的变化,越来越多的文献表明,与年龄相关的肠道菌群失调是导致老年人全身炎症状态的一个因素。然而,人们对肠道微生物群如何影响炎症衰老关注甚少。在这里,我们调查了关于衰老过程中炎症衰老与肠道微生物群之间关联的现有证据。我们系统地检索了 PubMed、Web of Science 和 Scopus,并检索到了 7 篇关于动物或人类的相关文章。动物研究报告称,拟杆菌、黏液螺旋菌、梭菌和葡萄球菌与促炎 MCP-1 呈正相关,阿克曼菌、真杆菌、布劳特氏菌和乳杆菌与 MCP-1 呈负相关。此外,“衰老”型微生物群与 IL6、IL-10、Th1、Th2、Treg、TNF-α、TGF-β、p16、SAMHD1、Eotaxin 和 RANTES 水平升高有关;TLR2、NF-κB 和 mTOR 被激活;与细胞周期蛋白 E 和 CDK2 水平降低有关。另一方面,对人类的研究表明,厚壁菌门的细菌与 IL-6 和 IL-8 呈正相关,而乳杆菌与 IL-8 呈负相关。我们的结论是,“衰老”型肠道微生物群的变化与炎症衰老有关。