Effect of β-blocker therapy in diabetic patients with stable coronary heart disease: a meta-analysis

Aaqib H Malik1, Suchith Shetty2, Kausik Kar1

  • 1Department of Medicine, Westchester Medical Center and New York Medical College, Valhalla, NY, USA.

Insights

Beta-blocker therapy in diabetic patients with stable coronary heart disease may increase cardiovascular mortality and major adverse cardiovascular events. Further research is needed to confirm these findings in this patient group.

Area of Science:

  • Cardiology
  • Diabetology
  • Pharmacology

Background:

  • Beta-blocker (BB) therapy is a standard treatment for coronary heart disease (CHD).
  • Limited evidence exists on the long-term benefits of BB therapy for diabetic patients with stable CHD.
  • This meta-analysis investigates the efficacy and safety of BB therapy in this specific population.

Purpose of the Study:

  • To summarize the current evidence on beta-blocker therapy in diabetic patients with stable coronary heart disease.
  • To evaluate the association between beta-blocker therapy and mortality and major adverse cardiovascular events in this cohort.

Main Methods:

  • A systematic meta-analysis was conducted following PRISMA and MOOSE guidelines.
  • Searches were performed in PubMed, Embase, and Cochrane Central databases.
  • Four non-randomized studies with 9515 participants were included, assessing all-cause mortality, cardiovascular mortality, and MACE.

Main Results:

  • Beta-blocker therapy was associated with a 27% increased risk of cardiovascular mortality and a 32% increased risk of MACE in diabetic patients with stable CHD (P < 0.05).
  • No significant reduction in all-cause mortality was observed (HR 1.12; P = 0.22).
  • The findings were based on four non-randomized studies, including post-hoc analyses and survey data.

Conclusions:

  • Beta-blocker therapy in diabetic patients with stable CHD may be associated with increased mortality.
  • Larger randomized controlled trials are essential to validate these findings and guide clinical practice.
Abstract

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