Salpeter Shelley R, Greyber Elizabeth, Pasternak Gary A, Salpeter Posthumous Edwin E
Medicine, Stanford University, and Santa Clara Valley Medical Center, 2400 Moorpark Ave, Suite 118, San Jose, CA, USA, 95128.
Cochrane Database Syst Rev. 2010 Jan 20(1):CD002967. doi: 10.1002/14651858.CD002967.pub3.
Metformin is an oral anti-hyperglycemic agent that has been shown to reduce total mortality compared to other anti-hyperglycemic agents, in the treatment of type 2 diabetes mellitus. Metformin, however, is thought to increase the risk of lactic acidosis, and has been considered to be contraindicated in many chronic hypoxemic conditions that may be associated with lactic acidosis, such as cardiovascular, renal, hepatic and pulmonary disease, and advancing age.
To assess the incidence of fatal and nonfatal lactic acidosis, and to evaluate blood lactate levels, for those on metformin treatment compared to placebo or non-metformin therapies.
A comprehensive search was performed of electronic databases to identify studies of metformin treatment. The search was augmented by scanning references of identified articles, and by contacting principal investigators.
Prospective trials and observational cohort studies in patients with type 2 diabetes of least one month duration were included if they evaluated metformin, alone or in combination with other treatments, compared to placebo or any other glucose-lowering therapy.
The incidence of fatal and nonfatal lactic acidosis was recorded as cases per patient-years, for metformin treatment and for non-metformin treatments. The upper limit for the true incidence of cases was calculated using Poisson statistics. In a second analysis lactate levels were measured as a net change from baseline or as mean treatment values (basal and stimulated by food or exercise) for treatment and comparison groups. The pooled results were recorded as a weighted mean difference (WMD) in mmol/L, using the fixed-effect model for continuous data.
Pooled data from 347 comparative trials and cohort studies revealed no cases of fatal or nonfatal lactic acidosis in 70,490 patient-years of metformin use or in 55,451 patients-years in the non-metformin group. Using Poisson statistics the upper limit for the true incidence of lactic acidosis per 100,000 patient-years was 4.3 cases in the metformin group and 5.4 cases in the non-metformin group. There was no difference in lactate levels, either as mean treatment levels or as a net change from baseline, for metformin compared to non-metformin therapies.
AUTHORS' CONCLUSIONS: There is no evidence from prospective comparative trials or from observational cohort studies that metformin is associated with an increased risk of lactic acidosis, or with increased levels of lactate, compared to other anti-hyperglycemic treatments.
二甲双胍是一种口服降糖药,在2型糖尿病治疗中,与其他降糖药相比,已显示可降低总死亡率。然而,二甲双胍被认为会增加乳酸酸中毒风险,并且在许多可能与乳酸酸中毒相关的慢性低氧血症情况下被视为禁忌,如心血管、肾脏、肝脏和肺部疾病以及老年。
评估接受二甲双胍治疗的患者与接受安慰剂或非二甲双胍治疗的患者相比,致命和非致命乳酸酸中毒的发生率,并评估血乳酸水平。
对电子数据库进行全面检索,以识别二甲双胍治疗的研究。通过扫描已识别文章的参考文献以及联系主要研究者来扩大检索范围。
纳入对病程至少1个月的2型糖尿病患者进行的前瞻性试验和观察性队列研究,这些研究评估了二甲双胍单独使用或与其他治疗联合使用,并与安慰剂或任何其他降糖治疗进行比较。
记录二甲双胍治疗组和非二甲双胍治疗组每患者年的致命和非致命乳酸酸中毒发生率(以病例数计)。使用泊松统计计算病例真实发生率的上限。在第二项分析中,测量治疗组和比较组乳酸水平相对于基线的净变化或平均治疗值(基础值以及食物或运动刺激后的数值)。使用连续数据的固定效应模型,将汇总结果记录为以mmol/L为单位的加权平均差(WMD)。
来自347项比较试验和队列研究的汇总数据显示,在使用二甲双胍的70490患者年或非二甲双胍组的55451患者年中,均未出现致命或非致命乳酸酸中毒病例。使用泊松统计,二甲双胍组每100000患者年乳酸酸中毒真实发生率的上限为4.3例,非二甲双胍组为5.4例。与非二甲双胍治疗相比,二甲双胍治疗的平均治疗水平或相对于基线的净变化的乳酸水平均无差异。
前瞻性比较试验或观察性队列研究均未提供证据表明,与其他降糖治疗相比,二甲双胍会增加乳酸酸中毒风险或提高乳酸水平。