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不同2型糖尿病阶段个体肠道微生物群的特征揭示了其与宿主的复杂关系。

Characterization of the Gut Microbiota of Individuals at Different T2D Stages Reveals a Complex Relationship with the Host.

作者信息

Chávez-Carbajal Alejandra, Pizano-Zárate María Luisa, Hernández-Quiroz Fernando, Ortiz-Luna Guillermo Federico, Morales-Hernández Rosa María, De Sales-Millán Amapola, Hernández-Trejo María, García-Vite Angelina, Beltrán-Lagunes Luis, Hoyo-Vadillo Carlos, García-Mena Jaime

机构信息

Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de México 07360, Mexico.

Departamento de Nutrición y Bioprogramación, Instituto Nacional de Perinatología, Ciudad de México 11000, Mexico.

出版信息

Microorganisms. 2020 Jan 10;8(1):94. doi: 10.3390/microorganisms8010094.

Abstract

In this work, we studied 217 Mexican subjects divided into six groups with different stages of glucose intolerance: 76 Controls (CO), 54 prediabetes (PRE), 14 T2D no medication (T2D-No-M), 14 T2D with Metformin (T2D-M), 22 T2D with polypharmacy (T2D-P), and 37 T2D with polypharmacy and insulin (T2D-P+I). We aimed to determine differences in the gut microbiota diversity for each condition. At the phylum level, we found that Firmicutes and Bacteroidetes outline major changes in the gut microbiota. The gut bacterial richness and diversity of individuals in the T2D-No-M group were lesser than other groups. Interestingly, we found a significant difference in the beta diversity of the gut microbiota among all groups. Higher abundance was found for in PRE, and spp. in T2D-No-M. In addition, we found associations of specific microbial taxa with clinical parameters. Finally, we report predicted metabolic pathways of gut microbiota linked to T2D-M and PRE conditions. Collectively, these results indicate that each group has specific predicted metabolic characteristics and gut bacteria populations for each phenotype. The results of this study could be used to define strategies to modulate gut microbiota through noninvasive treatments, such as dietary intervention, probiotics or prebiotics, and to improve glucose tolerance of individuals with prediabetes or T2D.

摘要

在这项研究中,我们对217名墨西哥受试者进行了研究,他们被分为六组,分别处于不同阶段的葡萄糖不耐受状态:76名对照组(CO)、54名糖尿病前期(PRE)、14名未用药的2型糖尿病患者(T2D-No-M)、14名使用二甲双胍的2型糖尿病患者(T2D-M)、22名使用多种药物的2型糖尿病患者(T2D-P)以及37名使用多种药物和胰岛素的2型糖尿病患者(T2D-P+I)。我们旨在确定每种情况下肠道微生物群多样性的差异。在门水平上,我们发现厚壁菌门和拟杆菌门勾勒出了肠道微生物群的主要变化。T2D-No-M组个体的肠道细菌丰富度和多样性低于其他组。有趣的是,我们发现所有组之间肠道微生物群的β多样性存在显著差异。在PRE组中发现[具体菌属1]丰度较高,在T2D-No-M组中发现[具体菌属2]丰度较高。此外,我们发现特定微生物分类群与临床参数之间存在关联。最后,我们报告了与T2D-M和PRE状态相关的肠道微生物群的预测代谢途径。总体而言,这些结果表明,每组对于每种表型都有特定的预测代谢特征和肠道细菌种群。本研究结果可用于确定通过饮食干预、益生菌或益生元等非侵入性治疗来调节肠道微生物群的策略,并改善糖尿病前期或2型糖尿病个体的葡萄糖耐量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86bd/7022408/b2ecba4135f2/microorganisms-08-00094-g001.jpg

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