Division of Nephrology, Department of Internal Medicine, Tri-service General Hospital Songshan Branch, Taipei, Taiwan; Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Department of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan; Research Center for Pharmacoeconomics, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Am J Med Sci. 2022 Nov;364(5):575-582. doi: 10.1016/j.amjms.2022.01.026. Epub 2022 Apr 25.
Evidence of metformin-associated lactic acidosis (MALA) in advanced chronic kidney disease (CKD) has been limited due to high mortality rate but rare incidence rate. The mechanism of increased MALA in advanced CKD is mainly based on the hypothesis of decreased drug elimination, which might also be confounded by increased comorbidities as CKD progresses. The goal of the study is to analyze the incidence and associated factors of lactic acidosis between metformin user and non-user with advanced CKD.
This study used a three million population-based, propensity score-matched cohort from 2008 to 2016. The primary outcome was laboratory-defined lactic acidosis. Relationships between the probability of lactic acidosis and various estimated glomerular filtration rate (eGFR) values in advanced CKD patients were also presented in regression analysis.
Adults with type 2 diabetes whose eGFR was <30 mL/min/1.73 m were enrolled in this study. After the process of propensity score matching, 7707 patients were divided into metformin and non-metformin groups. In linear regression model, metformin significantly increased the risk of lactic acidosis (p=0.0204) as the eGFR declined in advanced CKD over a mean follow up of over 600 days even after confounder adjustment with age, sex and comorbidities.
Metformin was associated with a significant increased risk of laboratory-defined lactic acidosis (p=0.0204) even after adjusting confounder such as age, sex and underlying comorbidities. This "REMIND" study reminds us that metformin-associated lactic acidosis is mainly caused by decreased drug renal elimination other than underlying comorbidities in advanced CKD patients.
由于高死亡率和低发病率,在晚期慢性肾脏病(CKD)中,二甲双胍相关乳酸酸中毒(MALA)的证据有限。在晚期 CKD 中,MALA 增加的机制主要基于药物清除减少的假设,随着 CKD 的进展,这种假设也可能因合并症的增加而变得复杂。本研究的目的是分析晚期 CKD 中使用和不使用二甲双胍患者乳酸酸中毒的发生率及相关因素。
本研究使用了 2008 年至 2016 年期间基于 300 万人口的倾向评分匹配队列。主要结局是实验室定义的乳酸酸中毒。在回归分析中,还展示了晚期 CKD 患者中乳酸酸中毒的概率与各种估计肾小球滤过率(eGFR)值之间的关系。
本研究纳入了 eGFR<30 mL/min/1.73 m2 的 2 型糖尿病成年患者。在进行倾向评分匹配后,7707 例患者被分为二甲双胍组和非二甲双胍组。在线性回归模型中,即使在调整年龄、性别和合并症等混杂因素后,随着 eGFR 在晚期 CKD 中下降,超过 600 天的平均随访期间,与 eGFR 下降相关,二甲双胍显著增加了乳酸酸中毒的风险(p=0.0204)。
即使在调整年龄、性别和潜在合并症等混杂因素后,二甲双胍与实验室定义的乳酸酸中毒显著相关(p=0.0204)。这项“REMIND”研究提醒我们,在晚期 CKD 患者中,二甲双胍相关乳酸酸中毒主要是由于药物肾清除减少引起的,而不是潜在的合并症。