Ejtahed Hanieh-Sadat, Tito Raul Y, Siadat Seyed-Davar, Hasani-Ranjbar Shirin, Hoseini-Tavassol Zahra, Rymenans Leen, Verbeke Kristin, Soroush Ahmad-Reza, Raes Jeroen, Larijani Bagher
Obesity and Eating Habits Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Department of Microbiology and Immunology, Rega Institute, KU Leuven, Leuven, Belgium.
Eur J Endocrinol. 2019 Mar;180(3):165-176. doi: 10.1530/EJE-18-0826.
The increasing prevalence of obesity over the past few decades constitutes a global health challenge. Pharmacological therapy is recommended to accompany life-style modification for obesity management. Here, we perform a clinical trial to investigate the effects of metformin on anthropometric indices and gut microbiota composition in non-diabetic, treatment-naive obese women with a low-calorie diet (LCD).
Randomized double-blind parallel-group clinical trial.
Forty-six obese women were randomly assigned to the metformin (500 mg/tab) or placebo groups using computer-generated random numbers. Subjects in both groups took two tablets per day for 2 months. Anthropometric measurements and collection of blood and fecal samples were done at the baseline and at the end of the trial. Gut microbiota composition was assessed using 16S rRNA amplicon sequencing.
Twenty-four and twenty-two subjects were included in the metformin + LCD and placebo + LCD groups, respectively; at the end of trial, 20 and 16 subjects were analyzed. The metformin + LCD and placebo + LCD caused a 4.5 and 2.6% decrease in BMI from the baseline values, respectively (P < 0.01). Insulin concentration decreased in the metformin + LCD group (P = 0.046). The overall fecal microbiota composition and diversity were unaffected in the metformin + LCD group. However, a significant specific increase in Escherichia/Shigella abundance was observed after metformin + LCD intervention (P = 0.026). Fecal acetate concentration, but not producers, was significantly higher in the placebo + LCD group, adjusted for baseline values and BMI (P = 0.002).
Despite the weight reduction after metformin intake, the overall fecal microbiota composition remained largely unchanged in obese women, with exception of changes in specific proteobacterial groups.
在过去几十年里,肥胖症患病率不断上升,这构成了一项全球性的健康挑战。对于肥胖症的管理,建议在改变生活方式的同时进行药物治疗。在此,我们开展一项临床试验,以研究二甲双胍对未患糖尿病、未接受过治疗的肥胖女性在低热量饮食(LCD)情况下人体测量指标和肠道微生物群组成的影响。
随机双盲平行组临床试验。
使用计算机生成的随机数将46名肥胖女性随机分为二甲双胍(500毫克/片)组或安慰剂组。两组受试者均每天服用两片,持续2个月。在基线期和试验结束时进行人体测量以及采集血液和粪便样本。使用16S rRNA扩增子测序评估肠道微生物群组成。
二甲双胍+LCD组和安慰剂+LCD组分别纳入24名和22名受试者;试验结束时,分别对20名和16名受试者进行了分析。与基线值相比,二甲双胍+LCD组和安慰剂+LCD组的体重指数分别下降了4.5%和2.6%(P<0.01)。二甲双胍+LCD组的胰岛素浓度有所下降(P=0.046)。二甲双胍+LCD组的总体粪便微生物群组成和多样性未受影响。然而,在二甲双胍+LCD干预后,观察到埃希氏菌属/志贺氏菌属丰度有显著的特定增加(P=0.026)。在根据基线值和体重指数进行调整后,安慰剂+LCD组的粪便乙酸盐浓度显著更高,但乙酸盐产生菌并非如此(P=0.002)。
尽管服用二甲双胍后体重有所减轻,但肥胖女性的总体粪便微生物群组成基本保持不变,只有特定变形菌菌群发生了变化。