肥胖青少年肠道菌群改变与代谢功能障碍相关

Diabetes Pub Date : 2025-05-01 DOI:10.2337/db24-0866
Alessandra Granato, Quin Yuhui Xie, Anthony Wong, Christopher Yau, Rebecca Noseworthy, Tina Chen, Connor Gianetto-Hill, Emma Allen-Vercoe, Cynthia J Guidos, Jill K Hamilton, Jayne S Danska
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引用次数: 0

摘要

儿童期肥胖与成年期肥胖、2型糖尿病(T2D)和未来代谢并发症相关。肠道微生物组是宿主代谢功能的调节剂,其细菌组成的改变与疾病风险相关。很少有研究调查代谢性疾病、炎症和年轻人肠道微生物群之间的关系,而这些联系可能起源于年轻人肠道微生物群。在这里,我们利用粪便DNA测序、绝对细菌定量以及免疫和代谢谱,对56名非糖尿病肥胖青少年的肠道微生物群进行了表征。基于巢式病例对照比较,我们观察到细菌绝对生物量的多对数阶变化依赖于宿主环境,并与细菌分类组成相关。高生物量的参与者表现出更健康的表型,肠道微生物群多样性更高,与炎症和致病性相关的分类群(如大肠杆菌)丰度更低,中性粒细胞活性水平更低。进一步的关联分析揭示了性别依赖性变异,在细菌生物量较低的男性青少年中,胰岛素抵抗、空腹甘油三酯和中性粒细胞活性标记物水平较高。总之,这些结果表明,肠道细菌的生物量和组成与T2D诊断前明显的代谢和炎症失调有关,并确定了肥胖青少年微生物组相关代谢功能障碍的性别差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic Dysfunction Associated With Alterations in Gut Microbiota in Adolescents With Obesity.

Obesity in childhood is associated with adulthood obesity, type 2 diabetes (T2D), and future metabolic complications. The gut microbiota is a modifier of host metabolic function with altered bacterial composition associated with disease risk. Few studies have investigated the relationships among metabolic disease, inflammation, and the gut microbiota in youth, in whom these connections likely originate. Here, we characterized the gut microbiome of a cohort of 56 adolescents with obesity and without diabetes using fecal DNA sequencing with absolute bacterial quantitation together with immune and metabolic profiling. We observed multi-log order variation in absolute bacterial biomass dependent on host environment and associated with bacterial taxonomic composition based on a nested case-control comparison. Participants with higher biomass displayed a healthier phenotype with higher gut microbiome diversity; lower abundance of taxa associated with inflammation and pathogenicity, such as Escherichia coli; and lower levels of neutrophil activities. Further association analysis revealed sex-dependent variation, with higher levels of insulin resistance, fasting triglycerides, and markers of neutrophil activities in male adolescents with lower bacterial biomass. Together, these results suggest that intestinal bacterial biomass and composition are associated with metabolic and inflammatory dysregulation evident before T2D diagnosis and identify sex differences in microbiome-associated metabolic dysfunction in adolescents with obesity.

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