代谢组
微生物群
代谢组学
糖尿病前期
2型糖尿病
生物
疾病
糖尿病
肠道微生物群
生物信息学
葡萄糖稳态
生理学
医学
内科学
内分泌学
胰岛素抵抗
作者
Hao Wu,Bo‐Min Lv,Luqian Zhi,Yikai Shao,Xinyan Liu,Matthias Mitteregger,Rima Chakaroun,Valentina Tremaroli,Stanley L. Hazen,Ru Wang,Göran Bergström,Fredrik Bäckhed
标识
DOI:10.1038/s41591-025-03642-6
摘要
Abstract Type 2 diabetes (T2D) is a complex disease shaped by genetic and environmental factors, including the gut microbiome. Recent research revealed pathophysiological heterogeneity and distinct subgroups in both T2D and prediabetes, prompting exploration of personalized risk factors. Using metabolomics in two Swedish cohorts ( n = 1,167), we identified over 500 blood metabolites associated with impaired glucose control, with approximately one-third linked to an altered gut microbiome. Our findings identified metabolic disruptions in microbiome–metabolome dynamics as potential mediators of compromised glucose homeostasis, as illustrated by the potential interactions between Hominifimenecus microfluidus and Blautia wexlerae via hippurate. Short-term lifestyle changes, for example, diet and exercise, modulated microbiome-associated metabolites in a lifestyle-specific manner. This study suggests that the microbiome–metabolome axis is a modifiable target for T2D management, with optimal health benefits achievable through a combination of lifestyle modifications.
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