den Hertog Heleen M, Vermeer S E, Zandbergen A A M, Achterberg Sefanja, Dippel Diederik W J, Algra Ale, Kappelle L J, Koudstaal Peter J
Department of Neurology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Int J Stroke. 2015 Jan;10(1):105-9. doi: 10.1111/ijs.12023. Epub 2013 Mar 15.
We aimed to assess the safety, feasibility, and effects on glucose metabolism of treatment with metformin in patients with TIA or minor ischemic stroke and impaired glucose tolerance.
We performed a multicenter, randomized, controlled, open-label phase II trial with blinded outcome assessment. Patients with TIA or minor ischemic stroke in the previous six months and impaired glucose tolerance (2-hour post-load glucose levels of 7.8-11.0 mmol/l) were randomized to metformin, in a daily dose of 2 g, or no metformin, for three months. Primary outcome measures were safety and feasibility of metformin, and the adjusted difference in 2-hour post-load glucose levels at three months. This trial is registered as an International Standard Randomized Controlled Trial Number 54960762.
Forty patients were enrolled; 19 patients were randomly assigned metformin. Nine patients in the metformin group had side effects, mostly gastrointestinal, leading to permanent discontinuation in four patients after 3-10 weeks. Treatment with metformin was associated with a significant reduction in 2-hour post-load glucose levels of 0·97 mmol/l (95% CI 0·11-1·83) in the on-treatment analysis, but not in the intention-to-treat analysis (0·71 mmol/l; 95% CI -0·36 to 1·78).
Treatment with metformin in patients with TIA or minor ischemic stroke and impaired glucose tolerance is safe, but leads to minor side effects. If tolerated, it may lead to a significant reduction in post-load glucose levels. This suggests that the role of metformin as potential therapeutic agent for secondary stroke prevention should be further explored.
我们旨在评估二甲双胍治疗短暂性脑缺血发作(TIA)或轻度缺血性卒中且糖耐量受损患者的安全性、可行性及对糖代谢的影响。
我们开展了一项多中心、随机、对照、开放标签的II期试验,并采用盲法评估结果。既往6个月内有TIA或轻度缺血性卒中且糖耐量受损(负荷后2小时血糖水平为7.8 - 11.0 mmol/L)的患者被随机分为接受每日剂量2 g二甲双胍治疗组或不接受二甲双胍治疗组,为期3个月。主要结局指标为二甲双胍的安全性和可行性,以及3个月时负荷后2小时血糖水平的校正差异。本试验已注册为国际标准随机对照试验编号54960762。
共纳入40例患者;19例患者被随机分配接受二甲双胍治疗。二甲双胍组有9例患者出现副作用,主要为胃肠道副作用,导致4例患者在3 - 10周后永久停药。在治疗分析中,二甲双胍治疗使负荷后2小时血糖水平显著降低0.97 mmol/L(95%可信区间0.11 - 1.83),但在意向性分析中未显示显著降低(0.71 mmol/L;95%可信区间 -0.36至1.78)。
二甲双胍治疗TIA或轻度缺血性卒中且糖耐量受损的患者是安全的,但会导致轻微副作用。如果能耐受,可能会使负荷后血糖水平显著降低。这表明二甲双胍作为二级卒中预防潜在治疗药物的作用应进一步探索。