Metformin use and cardiovascular events in patients with type 2 diabetes and chronic kidney disease

David M Charytan1, Scott D Solomon2, Peter Ivanovich3

  • 1Nephrology Division, Department of Medicine, NYU Langone Medical Center, New York, New York.

Insights

Metformin use in patients with diabetes and chronic kidney disease (CKD) was associated with reduced mortality and cardiovascular events. This study suggests metformin may be safer in CKD than previously thought, with a low risk of lactic acidosis.

Area of Science:

  • Nephrology
  • Cardiology
  • Endocrinology

Background:

  • Metformin, a common diabetes medication, is often avoided in patients with chronic kidney disease (CKD) due to concerns about lactic acidosis.
  • However, metformin may offer benefits for cardiovascular disease and kidney disease progression.

Purpose of the Study:

  • To compare cardiovascular events, mortality, and kidney disease progression in metformin users versus non-users with diabetes and CKD.
  • To assess the safety of metformin use in this patient population.

Main Methods:

  • Retrospective analysis of patients with diabetes and CKD from the Trial to Reduce Cardiovascular Events with Aranesp (TREAT) study.
  • Propensity matching and multivariable proportional hazards models were used to compare outcomes between metformin users and non-users.

Main Results:

  • Metformin users (n=591) showed lower rates of all-cause mortality, cardiovascular death, and cardiovascular events compared to non-users (n=3447) after propensity matching.
  • End-stage renal disease (ESRD) rates were similar between groups, and metformin use was not significantly associated with increased ESRD risk.
  • Two cases of lactic acidosis were observed in the entire cohort.

Conclusions:

  • Metformin may be safer for individuals with CKD than previously assumed.
  • Metformin use is associated with reduced mortality and cardiovascular events in patients with stage 3 CKD.
  • The risk of lactic acidosis appears low in this population.
Abstract

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