The Role of Metformin in Metformin-Associated Lactic Acidosis (MALA): Case Series and Formulation of a Model of Pathogenesis

被引:64
作者
Duong, Janna K. [1 ,2 ]
Furlong, Timothy J. [3 ]
Roberts, Darren M. [2 ,3 ,4 ]
Graham, Garry G. [1 ,2 ]
Greenfield, Jerry R. [5 ,6 ]
Williams, Kenneth M. [1 ,2 ]
Day, Richard O. [1 ,2 ,7 ]
机构
[1] Univ New S Wales, Sch Med Sci, Kensington, NSW 2033, Australia
[2] St Vincents Hosp, Dept Clin Pharmacol & Toxicol, Darlinghurst, NSW 2010, Australia
[3] St Vincents Hosp, Dept Nephrol, Darlinghurst, NSW 2010, Australia
[4] Concord Repatriat Gen Hosp, Dept Renal Med, Concord, NSW, Australia
[5] St Vincents Hosp, Dept Endocrinol, Darlinghurst, NSW 2010, Australia
[6] St Vincents Hosp, Garvan Inst Med Res, Diabet & Obes Res Program, Darlinghurst, NSW 2010, Australia
[7] Univ New S Wales, St Vincents Hosp, Sch Clin, Darlinghurst, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会; 澳大利亚研究理事会;
关键词
HIV-INFECTED PATIENTS; ACUTE-RENAL-FAILURE; MEMBRANE LOCALIZATION; DIABETES-MELLITUS; HEART-FAILURE; OVERDOSE; KIDNEY; RISK; THERAPY; CONTRAINDICATIONS;
D O I
10.1007/s40264-013-0038-6
中图分类号
R1 [预防医学、卫生学];
学科分类号
100235 [预防医学];
摘要
Background Lactic acidosis is an adverse event associated with metformin usage. Patients with metformin-associated lactic acidosis (MALA), however, often have other conditions contributing to the event. The relative contribution of metformin is often unclear. MALA is usually diagnosed without measuring the plasma concentrations of metformin. Objectives The objectives of this study were, first, to examine the plasma concentrations of metformin, lactate and creatinine and the arterial pH of patients with suspected MALA and, second, to review critically the mechanisms of MALA. Methods Patients who were suspected of having MALA were identified during the period October 2008 September 2011. Repeated blood samples were collected to determine the plasma concentrations of lactate, metformin and creatinine. The pH of arterial blood was also measured on several occasions in each patient. Results Patients (n = 15; 9 female, 6 male) were 70 +/- 12 years of age. There was one acute metformin overdose (estimated dose 5 g). Metformin was undetectable in one patient and one patient had therapeutic concentrations of metformin on admission (<5 mg/L). There were ten patients with chronic kidney disease, whereby the estimated glomerular filtration rate (eGFR) was less than 60 mL/min/1.73 m(2) before the acidotic event. Metformin doses ranged from 1 to 3 g daily (excluding the deliberate overdose). On admission, the mean plasma concentration of metformin on admission was 29.8 +/- 19.1 mg/L (mean +/- SD), the mean lactate concentration was 12. +/- 9 6.1 mmol/L and the mean pH was 7 +/- 0.2. The mean creatinine concentration on admission was 481 +/- 225 mu mol/L. The main pre-admission symptoms were vomiting and diarrhoea (n = 12). There were linear relationships between venous lactate, venous creatinine and arterial pH, with the venous plasma concentrations of metformin in most patients. Three patients died but metformin was unlikely to have been a significant factor. Discussion and review Most patients with MALA presented to the hospital with high metformin concentrations. The following factors appear to have been involved in the development of MALA in these patients: vomiting and diarrhoea, acute kidney injury, high doses or excessive accumulation of metformin, and acute disease states leading to tissue hypoxia. The extent of metformin accumulation in patients with MALA can be determined by investigating the concentrations of metformin. We suggest that the development of MALA is due to a positive feedback system involving one or more of these factors. While nausea is a common adverse effect of metformin, vomiting and diarrhoea out of the ordinary is a clear first sign of MALA. In this condition, dosage with metformin should be stopped and patients should receive urgent medical attention.
引用
收藏
页码:733 / 746
页数:14
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