4.7 Review

Metformin in Patients With Type 2 Diabetes and Kidney Disease A Systematic Review

Journal

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
Volume 312, Issue 24, Pages 2668-2675

Publisher

AMER MEDICAL ASSOC
DOI: 10.1001/jama.2014.15298

Keywords

-

Funding

  1. National Institutes of Health
  2. Yale Center for Clinical Investigation Scholar Award
  3. Pepper Center Research Career Development Award
  4. Boehringer Ingelheim
  5. Janssen Research and Development LLC
  6. sanofi-aventis Groupe
  7. Genentech
  8. Merck Sharp Dohme
  9. Medscape Cardiology
  10. Pri-Med Institute
  11. Brigham and Women's Hospital, Inc
  12. Duke Clinical Research Institute
  13. Cleveland Clinic Coordinating Center for Clinical Research
  14. University of Oxford
  15. Daiichi Sankyo
  16. Lilly USA
  17. Novo Nordisk
  18. F. Hoffmann La Roche
  19. Axio Research
  20. INC Research LLC
  21. GlaxoSmithKline
  22. Takeda Pharmaceuticals North America
  23. Bristol-Myers Squibb
  24. AstraZeneca
  25. Orexigen
  26. Lexicon
  27. Eisai
  28. Regeneron

Ask authors/readers for more resources

IMPORTANCE Metformin is widely viewed as the best initial pharmacological option to lower glucose concentrations in patients with type 2 diabetes mellitus. However, the drug is contraindicated in many individuals with impaired kidney function because of concerns of lactic acidosis. OBJECTIVE To assess the risk of lactic acidosis associated with metformin use in individuals with impaired kidney function. EVIDENCE ACQUISITION In July 2014, we searched the MEDLINE and Cochrane databases for English-language articles pertaining to metformin, kidney disease, and lactic acidosis in humans between 1950 and June 2014. We excluded reviews, letters, editorials, case reports, small case series, and manuscripts that did not directly pertain to the topic area or that met other exclusion criteria. Of an original 818 articles, 65 were included in this review, including pharmacokinetic/metabolic studies, large case series, retrospective studies, meta-analyses, and a clinical trial. RESULTS Although metformin is renally cleared, drug levels generally remain within the therapeutic range and lactate concentrations are not substantially increased when used in patients with mild to moderate chronic kidney disease (estimated glomerular filtration rates, 30-60 mL/min per 1.73m(2)). The overall incidence of lactic acidosis in metformin users varies across studies from approximately 3 per 100 000 person-years to 10 per 100 000 person-years and is generally indistinguishable from the background rate in the overall population with diabetes. Data suggesting an increased risk of lactic acidosis in metformin-treated patients with chronic kidney disease are limited, and no randomized controlled trials have been conducted to test the safety of metformin in patients with significantly impaired kidney function. Population-based studies demonstrate that metformin may be prescribed counter to prevailing guidelines suggesting a renal risk in up to 1 in 4 patients with type 2 diabetes mellitus-use which, in most reports, has not been associated with increased rates of lactic acidosis. Observational studies suggest a potential benefit from metformin on macrovascular outcomes, even in patients with prevalent renal contraindications for its use. CONCLUSIONS AND RELEVANCE Available evidence supports cautious expansion of metformin use in patients with mild to moderate chronic kidney disease, as defined by estimated glomerular filtration rate, with appropriate dosage reductions and careful follow-up of kidney function.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available