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Metformin Is Associated With Higher Relative Abundance of Mucin-Degrading Akkermansia muciniphila and Several Short-Chain Fatty Acid-Producing Microbiota in the Gut.二甲双胍与肠道中黏蛋白降解阿克曼氏菌( Akkermansia muciniphila )和几种产生短链脂肪酸的微生物的相对丰度增加有关。
Diabetes Care. 2017 Jan;40(1):54-62. doi: 10.2337/dc16-1324. Epub 2016 Nov 14.
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Shotgun Metagenomics of 250 Adult Twins Reveals Genetic and Environmental Impacts on the Gut Microbiome.对250对成年双胞胎进行的鸟枪法宏基因组学研究揭示了基因和环境对肠道微生物群的影响。
Cell Syst. 2016 Dec 21;3(6):572-584.e3. doi: 10.1016/j.cels.2016.10.004. Epub 2016 Nov 3.
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Gut microbiota signatures of longevity.长寿的肠道微生物群特征。
Curr Biol. 2016 Sep 26;26(18):R832-R833. doi: 10.1016/j.cub.2016.08.015.
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Probiotic and synbiotic therapy in critical illness: a systematic review and meta-analysis.危重症中的益生菌和合生制剂疗法:一项系统评价与荟萃分析。
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Fecal microbiota transplantation in inflammatory bowel disease: the quest for the holy grail.炎症性肠病中的粪便微生物群移植:追寻圣杯。
Mucosal Immunol. 2016 Nov;9(6):1360-1365. doi: 10.1038/mi.2016.67. Epub 2016 Jul 27.
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Universality of human microbial dynamics.人类微生物动态变化的普遍性。
Nature. 2016 Jun 9;534(7606):259-62. doi: 10.1038/nature18301.
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Age-related changes in gut microbiota composition from newborn to centenarian: a cross-sectional study.从新生儿到百岁老人肠道微生物群组成的年龄相关变化:一项横断面研究。
BMC Microbiol. 2016 May 25;16:90. doi: 10.1186/s12866-016-0708-5.
8
Culturing of 'unculturable' human microbiota reveals novel taxa and extensive sporulation.对“不可培养的”人类微生物群进行培养揭示了新的分类群和广泛的孢子形成。
Nature. 2016 May 26;533(7604):543-546. doi: 10.1038/nature17645. Epub 2016 May 4.
9
Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity.基于人群的宏基因组学分析揭示了肠道微生物组组成和多样性的标志物。
Science. 2016 Apr 29;352(6285):565-9. doi: 10.1126/science.aad3369. Epub 2016 Apr 28.
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Population-level analysis of gut microbiome variation.人群水平的肠道微生物组变异分析。
Science. 2016 Apr 29;352(6285):560-4. doi: 10.1126/science.aad3503. Epub 2016 Apr 28.

老年人的微生物组-健康相互作用。

Microbiome-health interactions in older people.

机构信息

School of Microbiology and APC Microbiome Institute, University College Cork, Cork, T12 YN60, Ireland.

出版信息

Cell Mol Life Sci. 2018 Jan;75(1):119-128. doi: 10.1007/s00018-017-2673-z. Epub 2017 Oct 6.

DOI:10.1007/s00018-017-2673-z
PMID:28986601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11105677/
Abstract

Alterations in the composition and function of the gut microbiome have been implicated in a range of conditions and diseases. Culture-dependent and culture-independent studies both showed that older people harbour a gut microbiome that differs in composition from that of younger adults. Detailed analyses have identified discrete microbiota subtypes that characterize intermediates between a high diversity microbiota found in healthy community-dwelling subjects and a low diversity microbiota typical for elderly living in long-term residential care. There are also alterations in the microbiome composition associated with biological age, independent of health status. Even after adjusting for confounding factors such as age and medication, trends in microbiota composition correlate with gradients in clinical metadata particularly frailty and inflammatory status. There are few known mechanisms by which these associations might be causative rather than consequential, and this is a subject of intensive research. The strongest candidate effectors are microbial metabolites that could impact host energy balance, act as signalling molecules to modulate host metabolism or inflammation, and potentially also impact on the gut-brain axis.

摘要

肠道微生物组的组成和功能的改变与一系列疾病和病症有关。依赖培养和非依赖培养的研究都表明,老年人的肠道微生物组在组成上与年轻人不同。详细的分析已经确定了离散的微生物群亚型,这些亚型特征是在健康的社区居住者中发现的高多样性微生物群和典型的长期居住在长期护理机构中的老年人的低多样性微生物群之间的中间状态。与健康状况无关,与生物年龄相关的微生物组组成也会发生改变。即使在调整了年龄和药物等混杂因素后,微生物组组成的趋势也与临床元数据的梯度相关,特别是脆弱性和炎症状态。这些关联可能是因果关系而不是结果关系的机制知之甚少,这是一个深入研究的课题。最强的候选效应物是微生物代谢产物,它们可能影响宿主的能量平衡,作为信号分子调节宿主代谢或炎症,并且还可能影响肠道-大脑轴。