Health Management Institute, the Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese People's Liberation Army General Hospital, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Tiantan Hospital, Advanced Innovation Center for Human Brain Protection, The Capital Medical University, Beijing, China.
Front Endocrinol (Lausanne). 2022 Jun 27;13:906310. doi: 10.3389/fendo.2022.906310. eCollection 2022.
Emerging evidence is examining the precise role of intestinal microbiota in the pathogenesis of type 2 diabetes. The aim of this study was to investigate the association of intestinal microbiota and microbiota-generated metabolites with glucose metabolism systematically in a large cross-sectional study in China. 1160 subjects were divided into three groups based on their glucose level: normal glucose group (n=504), prediabetes group (n=394), and diabetes group (n=262). Plasma concentrations of TMAO, choline, betaine, and carnitine were measured. Intestinal microbiota was measured in a subgroup of 161 controls, 144 prediabetes and 56 diabetes by using metagenomics sequencing. We identified that plasma choline [Per SD of log-transformed change: odds ratio 1.36 (95 confidence interval 1.16, 1.58)] was positively, while betaine [0.77 (0.66, 0.89)] was negatively associated with diabetes, independently of TMAO. Individuals with diabetes could be accurately distinguished from controls by integrating data on choline, and certain microbiota species, as well as traditional risk factors (AUC=0.971). KOs associated with the carbohydrate metabolism pathway were enhanced in individuals with high choline level. The functional shift in the carbohydrate metabolism pathway in high choline group was driven by species , and . We demonstrated the potential ability for classifying diabetic population by choline and specific species, and provided a novel insight of choline metabolism linking the microbiota to impaired glucose metabolism and diabetes.
越来越多的证据正在研究肠道微生物群在 2 型糖尿病发病机制中的精确作用。本研究旨在通过在中国的一项大型横断面研究系统地研究肠道微生物群及其产生的代谢物与葡萄糖代谢的相关性。1160 名受试者根据血糖水平分为三组:正常血糖组(n=504)、糖尿病前期组(n=394)和糖尿病组(n=262)。测量了 TMAO、胆碱、甜菜碱和肉碱的血浆浓度。在 161 名对照、144 名糖尿病前期和 56 名糖尿病患者的亚组中,使用宏基因组测序测量了肠道微生物群。我们发现,血浆胆碱[每 SD 的对数变化比:优势比 1.36(95%置信区间 1.16,1.58)]与糖尿病呈正相关,而甜菜碱[0.77(0.66,0.89)]与糖尿病呈负相关,独立于 TMAO。通过整合胆碱、某些微生物群物种以及传统危险因素的数据,可以准确地区分糖尿病患者和对照组(AUC=0.971)。高水平胆碱个体的碳水化合物代谢途径相关 KO 增加。高胆碱组碳水化合物代谢途径的功能变化是由物种 、 和 驱动的。我们证明了通过胆碱和特定物种对糖尿病人群进行分类的潜在能力,并提供了一个新的见解,即胆碱代谢将微生物群与受损的葡萄糖代谢和糖尿病联系起来。