Liu Yanmin, Qiu Qinwei, Chen Yang, Deng Yusheng, Huang Wei, Sun Chen, Shang Xiaoxiao, Chen Xinyan, Wang Chengrui, Han Lijuan, Chen Shiyan, Yuan Jiamin, Xu Fuping, Yang Zhimin, Fang Xiaodong, Huang Li
State Key Laboratory of Traditional Chinese Medicine Syndrome, State Key Laboratory of Dampness Syndrome of Chinese Medicine Syndrome, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
KMHD, Shenzhen, China.
Microbiol Spectr. 2025 Jul;13(7):e0145924. doi: 10.1128/spectrum.01459-24. Epub 2025 Jun 9.
Pre-diabetes (PD) represents a critical stage in the progression toward type 2 diabetes, with significant alterations observed in the human microbial community among pre-diabetic individuals in observational studies. However, understanding the interaction between human microbiota and the host during pre-diabetes remains limited. Therefore, this study aims to understand the alterations in the human microbial community during pre-diabetes, a critical stage toward type 2 diabetes. Using an integrated analysis of human microbiota and metabolomics data, we seek to identify the functional signature associated with PD and gain insights into potential mechanisms driving its progression to type 2 diabetes. These findings could inform the development of early intervention strategies for those at high risk. Samples were collected from pre-diabetes, diabetes, and healthy control groups. Through metagenome and 16S rRNA sequencing, we analyzed the gut microbial and tongue coating compositions, respectively. Untargeted metabolomics techniques were also applied for comprehensive plasma data. Using integrated multi-omics analysis, we aim to understand the metabolic potentials of the human microbiome, its molecular links with host targets, and their effects on pre-diabetes, thereby deepening our understanding of microbiome-host interactions in this context. The pre-diabetes group exhibited distinct clinical characteristics, particularly in blood glucose levels and a higher average level of γ-glutamyl transferase. We identified 509 intestinal bacterial species, with and showing higher abundance in the PD group. In tongue coating samples, we found 1,122 bacterial genera, with the PD group showing altered levels of and . Furthermore, we detected 795 metabolites, primarily involved in carbohydrate and lipid metabolism. Importantly, our integrated multi-omics analysis suggested 's role in modulating blood glucose through influencing carbohydrate metabolism. Our integrated multi-omics analysis revealed significant alterations in several regulatory pathways associated with pre-diabetes, particularly emphasizing the impact of gut bacterium on blood glucose levels through its influence on carbohydrate metabolism. These intricate relationships among gut microbiota, metabolites, and blood glucose levels underscore the significance of personalized treatment approaches and preventive strategies for pre-diabetes. The insights gained from this research hold considerable promise for advancing our understanding and management of pre-diabetes.IMPORTANCEThis study investigates alterations in the human microbial community during PD, a critical stage leading to type 2 diabetes. Through integrated analysis of metagenomic and metabolomics data from pre-diabetes, diabetes, and healthy control groups, we identified distinct clinical characteristics in the PD group, including elevated blood glucose levels and γ-glutamyl transferase. A total of 509 intestinal bacterial species were identified, with playing a key role in modulating blood glucose levels via its influence on carbohydrate metabolism. Our findings underscore the complex interactions among gut microbiota, metabolites, and blood glucose levels, highlighting the potential for personalized treatment approaches and early intervention strategies for individuals at high risk of developing type 2 diabetes.
糖尿病前期(PD)是向2型糖尿病进展的关键阶段,观察性研究发现糖尿病前期个体的人类微生物群落存在显著变化。然而,对于糖尿病前期期间人类微生物群与宿主之间的相互作用的了解仍然有限。因此,本研究旨在了解糖尿病前期(向2型糖尿病发展的关键阶段)期间人类微生物群落的变化。通过对人类微生物群和代谢组学数据的综合分析,我们试图确定与糖尿病前期相关的功能特征,并深入了解推动其进展为2型糖尿病的潜在机制。这些发现可为高危人群早期干预策略的制定提供依据。样本取自糖尿病前期、糖尿病和健康对照组。通过宏基因组和16S rRNA测序,我们分别分析了肠道微生物和舌苔的组成。非靶向代谢组学技术也应用于全面的血浆数据。通过综合多组学分析,我们旨在了解人类微生物组的代谢潜能、其与宿主靶点的分子联系以及它们对糖尿病前期的影响,从而加深我们对这一背景下微生物组与宿主相互作用的理解。糖尿病前期组表现出独特的临床特征,尤其是血糖水平和γ-谷氨酰转移酶平均水平较高。我们鉴定出509种肠道细菌,其中[具体细菌名称1]和[具体细菌名称2]在糖尿病前期组中丰度较高。在舌苔样本中,我们发现了1122个细菌属,糖尿病前期组中[具体细菌属1]和[具体细菌属2]的水平发生了变化。此外,我们检测到795种代谢物,主要参与碳水化合物和脂质代谢。重要的是,我们的综合多组学分析表明[具体细菌名称3]通过影响碳水化合物代谢在调节血糖中发挥作用。我们的综合多组学分析揭示了与糖尿病前期相关的几个调节途径的显著变化,特别强调肠道细菌[具体细菌名称3]通过影响碳水化合物代谢对血糖水平的影响。肠道微生物群、代谢物和血糖水平之间的这些复杂关系突出了糖尿病前期个性化治疗方法和预防策略的重要性。本研究获得的见解对于推进我们对糖尿病前期的理解和管理具有很大的前景。
重要性
本研究调查了糖尿病前期(向2型糖尿病发展的关键阶段)期间人类微生物群落的变化。通过对糖尿病前期、糖尿病和健康对照组的宏基因组和代谢组学数据进行综合分析,我们确定了糖尿病前期组的独特临床特征,包括血糖水平升高和γ-谷氨酰转移酶升高。共鉴定出509种肠道细菌,其中[具体细菌名称3]通过影响碳水化合物代谢在调节血糖水平中起关键作用。我们的研究结果强调了肠道微生物群、代谢物和血糖水平之间的复杂相互作用,突出了针对2型糖尿病高危个体的个性化治疗方法和早期干预策略的潜力。