Burton Jeffrey H, Johnson Matthew, Johnson Jolene, Hsia Daniel S, Greenway Frank L, Heiman Mark L
Pennington Biomedical Research Center, Baton Rouge, LA, USA.
Pennington Biomedical Research Center, Baton Rouge, LA, USA Louisiana State University Health Sciences Center, Baton Rouge, LA, USA.
J Diabetes Sci Technol. 2015 Jul;9(4):808-14. doi: 10.1177/1932296815577425. Epub 2015 Mar 23.
Adverse effects of metformin are primarily related to gastrointestinal (GI) intolerance that could limit titration to an efficacious dose or cause discontinuation of the medication. Because some metformin side effects may be attributable to shifts in the GI microbiome, we tested whether a GI microbiome modulator (GIMM) used in combination with metformin would ameliorate the GI symptoms.
A 2-period crossover study design was used with 2 treatment sequences, either placebo in period 1 followed by GIMM in period 2 or vice versa. Study periods lasted for 2 weeks, with a 2-week washout period between. During the first week, type 2 diabetes patients (T2D) who experienced metformin GI intolerance took 500 mg metformin along with their assigned NM504 (GIMM) or placebo treatment with breakfast and with dinner. In the second week, the 10 subjects took 500 mg metformin (t.i.d.), with GIMM or placebo consumed with the first and third daily metformin doses. Subjects were permitted to discontinue metformin dosing if it became intolerable.
The combination of metformin and GIMM treatment produced a significantly better tolerance score to metformin than the placebo combination (6.78 ± 0.65 [mean ± SEM] versus 4.45 ± 0.69, P = .0006). Mean fasting glucose levels were significantly (P < .02) lower with the metformin-GIMM combination (121.3 ± 7.8 mg/dl) than with metformin-placebo (151.9 ± 7.8 mg/dl).
Combining a GI microbiome modulator with metformin might allow the greater use of metformin in T2D patients and improve treatment of the disease.
二甲双胍的不良反应主要与胃肠道(GI)不耐受有关,这可能会限制剂量滴定至有效剂量或导致停药。由于一些二甲双胍的副作用可能归因于胃肠道微生物群的变化,我们测试了一种胃肠道微生物群调节剂(GIMM)与二甲双胍联合使用是否能改善胃肠道症状。
采用两阶段交叉研究设计,有两种治疗顺序,即第1阶段为安慰剂,第2阶段为GIMM,或反之。研究阶段持续2周,中间有2周的洗脱期。在第一周,经历二甲双胍胃肠道不耐受的2型糖尿病患者(T2D)在早餐和晚餐时服用500mg二甲双胍以及分配的NM504(GIMM)或安慰剂治疗。在第二周,10名受试者服用500mg二甲双胍(每日三次),在每日第一剂和第三剂二甲双胍时服用GIMM或安慰剂。如果二甲双胍变得无法耐受,受试者可停止给药。
与安慰剂联合使用相比,二甲双胍和GIMM联合治疗对二甲双胍的耐受性评分显著更高(6.78±0.65[平均值±标准误]对4.45±0.69,P = 0.0006)。二甲双胍 - GIMM联合治疗组的平均空腹血糖水平(121.3±7.8mg/dl)显著低于二甲双胍 - 安慰剂组(151.9±7.8mg/dl)(P < 0.02)。
将胃肠道微生物群调节剂与二甲双胍联合使用可能会使二甲双胍在T2D患者中得到更广泛的应用,并改善疾病治疗效果。