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Cardiac secretion of adrenomedullin in human heart failure
M Jougasaki1, R J Rodeheffer, M M Redfield
1Cardiorenal Research Laboratory, Division of Cardiovascular Diseases, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
Insights
The failing human heart secretes adrenomedullin (ADM), a peptide that helps regulate blood pressure and salt balance. Plasma ADM levels increase with congestive heart failure (CHF) severity, indicating a new cardiac endocrine system activated in CHF.
Area of Science:
- Cardiology
- Endocrinology
- Physiology
Background:
- Adrenomedullin (ADM) is an endogenous peptide with vasorelaxing and natriuretic properties.
- Elevated plasma ADM and myocardial ADM staining are observed in severe congestive heart failure (CHF).
Purpose of the Study:
- To investigate whether the failing human ventricle secretes ADM.
- To determine if circulating ADM levels increase progressively with clinical CHF severity.
Main Methods:
- Measured plasma ADM levels in normal subjects and patients with varying degrees of CHF (NYHA classes II, III, and IV).
- Collected plasma samples from the aorta, coronary sinus, and anterior interventricular vein in CHF patients to assess ADM secretion.
Main Results:
- Plasma ADM was significantly elevated in CHF patients compared to normal subjects.
- ADM levels increased across mild, moderate, and severe CHF stages, with a marked rise in severe CHF (NYHA class IV).
- A significant increase (step-up) in plasma ADM was observed from the aorta to the anterior interventricular vein and coronary sinus in CHF patients, indicating cardiac secretion.
Conclusions:
- The failing human heart actively secretes ADM in CHF, contributing to elevated circulating levels.
- This study identifies a novel cardiac endocrine system activated in CHF, potentially playing a role in cardiorenal regulation.
Abstract:
Adrenomedullin (ADM) is a newly discovered endogenous vasorelaxing and natriuretic peptide. Recently, we have reported that plasma ADM is increased in severe congestive heart failure (CHF) in humans and that increased immunohistochemical staining is observed in the failing human ventricular myocardium. The present study was designed to test the hypothesis that the failing human ventricle secretes ADM and that circulating ADM progressively increases with the severity of clinical CHF. Plasma ADM was significantly increased in human CHF (39.8 +/- 3.6 pg/ml, P < 0.001 vs. normal) as compared with normal subjects (14.4 +/- 2.7 pg/ml). Plasma ADM was increased in mild CHF (NYHA class II, 30.1 +/- 3.4 pg/ml, P < 0.01 vs. normal), moderate CHF (NYHA class III, 31.5 +/- 3.0 pg/ml, P < 0.01 vs. normal), and severe CHF (NYHA class IV, 66.1 +/- 9.4 pg/ml, P < 0.001 vs. normal). In 13 patients with CHF in whom plasma samples were obtained from aorta (AO), coronary sinus (CS) and anterior interventricular vein (AIV), there was a significant step-up in plasma ADM between AO and AIV (50.6 +/- 9.3 pg/ml and 62.1 +/- 11.1 pg/ml, respectively, P < 0.01) and between AO and CS (50.6 +/- 9.3 pg/ml and 58.6 +/- 11.4 pg/ml, respectively, P < 0.05). The current study demonstrates that the failing human heart secretes ADM in human CHF suggesting contribution to the increase in plasma ADM, and indicates for the first time an additional endocrine system of cardiac origin which is activated in human CHF and may function in cardiorenal regulation.
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