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Early neurohormonal effects of trandolapril in patients with left ventricular dysfunction and a recent acute
A Sigurdsson1, S V Eriksson, C Hall
1Department of Medicine, Division of Cardiology, Landspitalinn v. Hringbraut, 101, Reykjavik, Iceland. axelfsig@rsp.is
Insights
Angiotensin-converting enzyme inhibitors improve survival after myocardial infarction, but early neurohormonal changes are not the primary mechanism. Short-term trandolapril did not alter key hormone levels, suggesting other factors drive long-term benefits.
Area of Science:
- Cardiology
- Pharmacology
- Biochemistry
Background:
- Angiotensin-converting enzyme (ACE) inhibitors improve survival in post-myocardial infarction (MI) patients with left ventricular dysfunction.
- The exact mechanisms, including neurohormonal effects and hemodynamic unloading, require further elucidation.
Purpose of the Study:
- To assess trandolapril's effect on plasma atrial natriuretic peptide levels post-MI.
- To evaluate trandolapril's impact on other neurohormones, vasoactive peptides, and enzymes relevant to cardiac remodeling and heart failure.
Main Methods:
- 119 patients with acute MI and left ventricular dysfunction were randomized to trandolapril or placebo for 21 days.
- Blood samples were collected pre-treatment and post-treatment to measure various biomarkers.
- Echocardiography assessed left ventricular function (wall motion index).
Main Results:
- No significant difference in atrial natriuretic peptide levels between groups.
- Trandolapril suppressed ACE activity and increased plasma renin activity.
- Levels of N-terminal pro-atrial natriuretic peptide, BNP, aldosterone, and catecholamines remained unchanged.
Conclusions:
- Early (2-3 weeks) ACE inhibition with trandolapril does not significantly alter key circulatory neurohormone levels post-MI.
- Neurohormonal activation at baseline correlates with left ventricular dysfunction and heart failure.
- Early modulation of these specific neurohormones may not be the primary driver of long-term ACE inhibitor efficacy, though certain markers may identify suitable patients.
Abstract:
Angiotensin-converting enzyme inhibitors improve long-term survival in patients with left ventricular dysfunction after a myocardial infarction, but their mechanism of action is not entirely clear. The neurohormonal effects may be important in this respect, as well as an early hemodynamic unloading induced by these drugs. The primary objective was to assess the effect of trandolapril on plasma levels of atrial natriuretic peptide. A secondary objective was to assess the effects of trandolapril on selected neurohormones, vasoactive peptides and enzymes, which may be important in the development of left ventricular remodeling and heart failure following an acute myocardial infarction. A total of 119 patients with an acute myocardial infarction and a wall motion index < or =1.2 (16-segment echocardiographic model) were randomized to double blind treatment with trandolapril or placebo within 3-7 days after the onset of infarction. Blind treatment was discontinued 21 days after the index infarction. Venous blood samples were collected at rest, before randomization and on the day after treatment was discontinued. At the end of the study, there were no differences in plasma levels of atrial natriuretic peptide between the two treatment groups. Angiotensin-converting enzyme activity was suppressed and plasma renin activity was higher in the trandolapril group. No differences in plasma levels of N-terminal pro-atrial natriuretic peptide, brain natriuretic peptide, aldosterone, noradrenaline, adrenaline, vasopressin, big endothelin-1 and neuropeptide Y were found between the two treatment groups. There were positive correlations between several markers of neurohormonal activation at baseline and variables expressing left ventricular dysfunction and clinical heart failure. Neurohormonal activation is related to left ventricular dysfunction. The effects of 2-3 weeks of angiotensin-converting enzyme inhibition on neurohormonal activation does not predict the already established beneficial long-term effects after myocardial infarction. Thus, early modulation of circulatory neurohormone levels may not be a major mechanism for the efficacy of angiotensin-converting enzyme inhibitors in these patients. Selected plasma hormone markers may still be used to identify patients who might get the greatest benefit from treatment.
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