Liu Qing, Hua Yifei, He Rongbo, Xiang Liqian, Li Shaoqing, Zhang Ying, Chen Rourou, Qian Li, Jiang Xiaomeng, Wang Congyi, Li Yangyang, Wu Hao, Liu Yu
Department of Endocrinology, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211100, China.
Department of Endocrinology, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211100, China; Department of Endocrinology, The Fourth Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing, Jiangsu Province 211800, China.
Cell Rep Med. 2025 May 20;6(5):102130. doi: 10.1016/j.xcrm.2025.102130. Epub 2025 May 9.
This study investigates the roles of gut microbiome and secondary bile acid dysfunctions in type 1 diabetes (T1D) and explores targeted interventions to address them. It finds that T1D is associated with reduced gut microbial diversity and imbalance favoring harmful bacteria over beneficial ones. Additionally, patients with T1D exhibited impaired secondary bile acid metabolism. Interventions aimed at modulating the gut microbiome and metabolites are safe and improve glycemic control, reduce daily insulin dose, and reduce inflammation. These interventions reshape the gut microbiome toward a healthier state and enhance secondary bile acid production. Responders to the interventions show increased levels of beneficial bacteria and secondary bile acids, along with improved C-peptide responses. Overall, these findings suggest that targeted modulation of the gut microbiome and secondary bile acid metabolism could be a promising therapeutic approach for T1D management. The trial is registered at Chinese Clinical Trial Registry (ChiCTR-ONN-17011279).
本研究调查了肠道微生物群和继发性胆汁酸功能障碍在1型糖尿病(T1D)中的作用,并探索针对这些问题的靶向干预措施。研究发现,T1D与肠道微生物多样性降低以及有害菌多于有益菌的失衡有关。此外,T1D患者的继发性胆汁酸代谢受损。旨在调节肠道微生物群和代谢物的干预措施是安全的,可改善血糖控制、减少每日胰岛素剂量并减轻炎症。这些干预措施使肠道微生物群重塑为更健康的状态,并增强继发性胆汁酸的产生。对干预措施有反应者的有益菌和继发性胆汁酸水平升高,同时C肽反应改善。总体而言,这些发现表明,对肠道微生物群和继发性胆汁酸代谢进行靶向调节可能是管理T1D的一种有前景的治疗方法。该试验已在中国临床试验注册中心注册(ChiCTR-ONN-17011279)。