Irbesartan improves arterial compliance more than lisinopril

Khalid Ali1, Chakravarthi Rajkumar, Francesco Fantin

  • 1Academic Department of Geriatrics, Brighton and Sussex Medical School, Brighton, UK. khalid.ali@bsuh.nhs.uk

Insights

Irbesartan significantly improved arterial compliance in both elastic and muscular arteries. Lisinopril, however, only improved compliance in elastic arteries, indicating differential effects of these antihypertensive agents.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacology

Background:

  • Antihypertensive agents are known to reduce arterial stiffness.
  • Arterial compliance is a key indicator of cardiovascular health.
  • Angiotensin receptor blockers (ARBs) and angiotensin converting enzyme inhibitors (ACEIs) are common classes of antihypertensive drugs.

Purpose of the Study:

  • To investigate the effects of irbesartan (an ARB) and lisinopril (an ACEI) on arterial compliance.
  • To compare the efficacy of irbesartan and lisinopril in improving arterial stiffness in hypertensive patients.

Main Methods:

  • A randomized, double-blind, double-dummy, controlled crossover trial was conducted.
  • Fifteen hypertensive patients received either irbesartan or lisinopril for 12 weeks, followed by a crossover period.
  • Pulse wave velocity (PWV) was measured in the carotid-femoral (CF), carotid-radial (CR), and femoral dorsalis-pedis (FD) arteries.

Main Results:

  • Both irbesartan and lisinopril reduced systolic blood pressure (SBP).
  • Irbesartan and lisinopril significantly reduced PWV in the elastic arteries (CF).
  • Irbesartan demonstrated significant reductions in PWV for both elastic (CR) and muscular (FD) arteries, while lisinopril did not show significant effects on CR and FD PWV after SBP adjustment.

Conclusions:

  • Irbesartan effectively improved arterial compliance in both elastic and muscular arterial systems.
  • Lisinopril improved arterial compliance primarily in the elastic arteries.
  • The findings suggest differential effects of ARBs and ACEIs on arterial stiffness beyond blood pressure reduction.
Abstract

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