Cornejo-Pareja Isabel, Martín-Núñez Gracia M, Roca-Rodríguez M Mar, Cardona Fernando, Coin-Aragüez Leticia, Sánchez-Alcoholado Lidia, Gutiérrez-Repiso Carolina, Muñoz-Garach Araceli, Fernández-García José C, Moreno-Indias Isabel, Tinahones Francisco J
Department of Endocrinology and Nutrition, Virgen de la Victoria Hospital (IBIMA), Malaga University, 29010 Malaga, Spain.
Centro de Investigacion Biomédica en Red de la Fisiopatología de la Obesidad y Nutrición (CIBEROBN CB06/003), Instituto de Salud Carlos III, 28029 Madrid, Spain.
J Clin Med. 2019 Apr 4;8(4):451. doi: 10.3390/jcm8040451.
Changes in the intestinal microbial community and some metabolic disturbances, including obesity and type2 diabetes, are related. Glucagon-like peptide-1 (GLP-1) regulates glucose homeostasis. Microbiota have been linked to incretin secretion. Antibiotic use causes changes in microbial diversity and composition. Our aim was to evaluate the relationship between microbiota changes and GLP-1 secretion. A prospective case-control study with a -positive patient model involving subjects under eradication therapy (omeprazole, clarithromycin, and amoxicillin). Forty patients with infection and 20 matched participants, but negative for antigen. Patients were evaluated before and two months after treatment. We analyzed anthropometric measurements, carbohydrate metabolism, lipid profile, and C-reactive protein. Gut microbiota composition was analyzed through 16S rRNA amplicon sequencing (IlluminaMiSeq). Eradication treatment for decreased bacterial richness (Chao1, 0.041). Changes in gut microbiota profiles were observed at phylum, family, genus and species levels. GLP-1 secretion and variables of carbohydrate metabolism were improved. Correlations were seen between GLP-1 changes and variations within microbial community abundances, specifically , the genus, and family. A conventional treatment to eradicate could improve carbohydrate metabolism possibly in relation with an increase in GLP-1 secretion. GLP-1 secretion may be related to alterations in intestinal microbiota, specifically and .
肠道微生物群落的变化与包括肥胖和2型糖尿病在内的一些代谢紊乱有关。胰高血糖素样肽-1(GLP-1)调节葡萄糖稳态。微生物群与肠促胰岛素分泌有关。抗生素的使用会导致微生物多样性和组成的变化。我们的目的是评估微生物群变化与GLP-1分泌之间的关系。一项前瞻性病例对照研究,采用阳性患者模型,纳入接受根除治疗(奥美拉唑、克拉霉素和阿莫西林)的受试者。40例感染患者和20例匹配的参与者,但抗原检测为阴性。在治疗前和治疗后两个月对患者进行评估。我们分析了人体测量学指标、碳水化合物代谢、血脂谱和C反应蛋白。通过16S rRNA扩增子测序(Illumina MiSeq)分析肠道微生物群组成。根除治疗降低了细菌丰富度(Chao1,P = 0.041)。在门、科、属和种水平上观察到肠道微生物群谱的变化。GLP-1分泌和碳水化合物代谢变量得到改善。观察到GLP-1变化与微生物群落丰度变化之间的相关性,特别是普雷沃氏菌属和瘤胃球菌科。一种根除幽门螺杆菌的传统治疗方法可能通过增加GLP-1分泌来改善碳水化合物代谢。GLP-1分泌可能与肠道微生物群的改变有关,特别是普雷沃氏菌属和瘤胃球菌科。