Alterations in the Gut Microbiota Composition in Obesity with and without Type 2 Diabetes: A Pilot Study.

Diabetes Metab Syndr Obes

Department of Endocrinology, Beijing Tsinghua Changgung Hospital, Tsinghua University, Beijing, People's Republic of China.

Published: October 2024

Purpose: Obesity has become a major public health concern worldwide, increasing the risk of T2DM. Growing evidence indicates gut microbiota dysbiosis is related to metabolic disorders. We aimed to firstly investigate the compositional and functional features of the gut microbiome between obesity with and without T2DM in the Chinese population.

Methods: A total of 32 obese individuals accompanied with T2DM and 18 age and gender-matched obesity with normal glucose tolerance (NGT) were enrolled. Fecal samples were collected, and the gut microbiota profile was determined using the Illumina MiSeq platform based on V3-V4 bacterial 16S rRNA gene.

Results: Compared with obesity- NGT, obesity-T2DM showed a significantly higher alpha diversity. Principal coordinates analysis based on both Bray-Curtis distance and weighted Unifrac revealed that the global microbial composition was significantly different between the two groups (P = 0.007 and P = 0.005, respectively). At the phylum level, Obesity-T2DM patients exhibited a significant decrease in , and a pronounced increase in . Regarding the genus level, and were found to increase considerably, while and had an evident decrease in Obesity-T2DM. Furthermore, Spearman correlation analysis revealed that and were negatively associated with HbA1c and fasting blood glucose.

Conclusion: We found clear differences in the gut microbiota composition in obesity-T2DM compared with obesity-NGT. Obesity accompanied with T2DM may aggravate the obesity-associated gut microbiota, and gut microbiota is expected to be a promising novel intervention target for obese management. However, larger sample size and more in-depth taxonomic identification studies are warranted.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11514687PMC
http://dx.doi.org/10.2147/DMSO.S477494DOI Listing

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