Effect of angiotensin receptor blockers on cardiovascular events in patients undergoing hemodialysis: an open-label

Hiromichi Suzuki1, Yoshihiko Kanno, Soichi Sugahara

  • 1Department of Nephrology, School of Medicine, Faculty of Medicine, Saitama Medical University, Saitama, Japan. iromichi@saitama-med.ac.jp

Insights

Angiotensin receptor blockers (ARBs) significantly reduced cardiovascular disease (CVD) events in hemodialysis (HD) patients. While promising, larger studies are needed to confirm these findings for patients with kidney failure on HD.

Area of Science:

  • Nephrology
  • Cardiology
  • Pharmacology

Background:

  • Cardiovascular disease (CVD) is the primary cause of death in hemodialysis (HD) patients.
  • Angiotensin receptor blockers (ARBs) are known to reduce CVD events in diabetic patients with chronic kidney disease.
  • The efficacy of ARBs in HD patients with kidney failure remains unknown.

Purpose of the Study:

  • To investigate the effect of ARBs on CVD events in patients undergoing long-term HD.
  • To evaluate ARBs as a potential intervention for reducing cardiovascular mortality in this high-risk population.

Main Methods:

  • An open-label randomized trial was conducted.
  • 180 patients undergoing HD (30-80 years old) received ARBs (valsartan, candesartan, losartan), while 180 served as controls.
  • Patients were stratified by sex, age, systolic blood pressure, and diabetes.

Main Results:

  • Treatment with ARBs was associated with a significant reduction in fatal and nonfatal CVD events (HR, 0.51; P = 0.002).
  • The ARB group experienced 19% CVD events compared to 33% in the non-ARB group.
  • All-cause mortality showed a trend towards reduction in the ARB group (HR, 0.64; P = 0.1).

Conclusions:

  • ARBs may be effective in reducing nonfatal CVD events for patients on long-term HD.
  • Limitations include a small sample size and open-label design, suggesting the observed effect might be spurious.
  • Larger, placebo-controlled trials are necessary to validate these findings.
Abstract

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