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揭示与健康人群中 PPARD 和 PARGC1A 基因多态性相关的肠道微生物组特征。

Unraveling Gut Microbiota Signatures Associated with PPARD and PARGC1A Genetic Polymorphisms in a Healthy Population.

机构信息

MAS Microbiota Research Group, Universidad Europea de Madrid, Calle Tajo s/n, Villaviciosa de Odón, 28670 Madrid, Spain.

出版信息

Genes (Basel). 2022 Feb 1;13(2):289. doi: 10.3390/genes13020289.

Abstract

Recent studies have revealed the importance of the gut microbiota in the regulation of metabolic phenotypes of highly prevalent metabolic diseases such as obesity, type II diabetes mellitus (T2DM) and cardiovascular disease. Peroxisome proliferator-activated receptors (PPARs) are a family of ligand-activated nuclear receptors that interact with PPAR-γ co-activator-1α (PPARGC1A) to regulate lipid and glucose metabolism. Genetic polymorphisms in (rs 2267668; A/G) and (rs 8192678; G/A) are linked to T2DM. We studied the association between the single-nucleotide polymorphisms (SNPs) rs 2267668 and rs 8192678 and microbiota signatures and their relation to predicted metagenome functions, with the aim of determining possible microbial markers in a healthy population. Body composition, physical exercise and diet were characterized as potential confounders. Microbiota analysis of subjects with (rs 8192678) and (rs 2267668) SNPs revealed certain taxa associated with the development of insulin resistance and T2DM. Kyoto encyclopedia of gene and genomes analysis of metabolic pathways predicted from metagenomes highlighted an overrepresentation of ABC sugar transporters for the (rs 8192678) SNP. Our findings suggest an association between sugar metabolism and the rs 8192678 (G/A) genotype and support the notion of specific microbiota signatures as factors related to the onset of T2DM.

摘要

最近的研究揭示了肠道微生物群在调节肥胖、2 型糖尿病 (T2DM) 和心血管疾病等高发代谢性疾病的代谢表型方面的重要性。过氧化物酶体增殖物激活受体 (PPARs) 是一组配体激活的核受体,与 PPAR-γ 共激活因子-1α (PPARGC1A) 相互作用,调节脂质和葡萄糖代谢。基因多态性(rs2267668;A/G)和(rs8192678;G/A)与 T2DM 相关。我们研究了单核苷酸多态性 (SNP) rs2267668 和 rs8192678 与微生物群特征及其与预测宏基因组功能的关系,目的是确定健康人群中可能的微生物标志物。身体成分、体育锻炼和饮食被认为是潜在的混杂因素。对携带(rs8192678)和(rs2267668)SNP 的受试者的微生物组分析揭示了与胰岛素抵抗和 T2DM 发展相关的某些分类群。从宏基因组预测的代谢途径京都基因与基因组百科全书分析突出了 ABC 糖转运体对(rs8192678)SNP 的过度表达。我们的研究结果表明,糖代谢与 rs8192678(G/A)基因型之间存在关联,并支持特定微生物群特征作为与 T2DM 发病相关的因素的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d0e/8871880/fe2557215963/genes-13-00289-g001.jpg

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