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Angiotensin-converting enzyme inhibitors, left ventricular dysfunction, and early heart failure
J G Cleland1, D Shah, S Krikler
1Department of Medicine (Cardiology), Hammersmith Hospital, London, United Kingdom.
The American Journal of Cardiology
|October 8, 1992
Summary
Lisinopril, an angiotensin-converting enzyme inhibitor, showed a trend toward improved exercise time and significantly increased peak oxygen consumption in patients with impaired left ventricular systolic function during high-intensity exercise.
Area of Science:
- Cardiology
- Pharmacology
- Exercise Physiology
Background:
- Left ventricular systolic dysfunction (LVSD) significantly impacts exercise capacity.
- Angiotensin-converting enzyme (ACE) inhibitors are standard treatments for heart failure.
- The specific effects of ACE inhibitors like lisinopril on exercise performance in LVSD patients require further elucidation.
Purpose of the Study:
- To investigate the impact of the ACE inhibitor lisinopril on exercise performance in patients with major impairment of left ventricular systolic function.
- To assess the hemodynamic and hormonal effects of lisinopril in this patient population.
Main Methods:
- A randomized, double-blind, crossover study involving 18 patients with LVSD.
- Patients received either lisinopril (2.5-10 mg daily) or placebo for 6 weeks.
- Exercise performance was evaluated using low- and high-intensity protocols, alongside hemodynamic and hormonal measurements.
Main Results:
- Lisinopril did not significantly alter resting blood pressure or heart rate.
- No effect on exercise duration was observed during low-intensity exercise.
- A trend toward improved exercise time and a significant increase in peak oxygen consumption were noted during high-intensity exercise.
- Lisinopril increased renal blood flow, decreased glomerular filtration rate, and altered plasma hormone levels (decreased angiotensin II, aldosterone, atrial natriuretic peptide; increased active renin).
Conclusions:
- Lisinopril may offer benefits for exercise capacity, particularly peak oxygen consumption, in patients with LVSD during high-intensity activities.
- The drug modulates the renin-angiotensin-aldosterone system and impacts renal hemodynamics.
- Further research is warranted to confirm these findings and explore clinical implications.