4.7 Article

Increased level of pericardial insulin-like growth factor-1 in patients with left ventricular dysfunction and advanced heart failure

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 48, Issue 7, Pages 1387-1395

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2006.06.048

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OBJECTIVES To test the hypothesis that the cardiac insulin-like growth factor-1 (TGF-1) system is up-regulated in the failing heart, we measured the pericardial (cardiac) and plasma (circulating) 1GF-1 levels in coronary artery disease patients. BACKGROUND Local IGF-1 systems are regulated differently from the systemic IGF-1 system. The cardiac 1GF-1 system is up-regulated by the increased left ventricular (LV) wall stress. However, it remains unknown how this system is affected in LV dysfunction and heart failure. METHODS We measured the plasma and pericardial fluid levels of IGF-1 and brain natriuretic peptide (BNP) in 87 coronary artery disease patients undergoing cardiac surgery, and examined their relationships with LV function and heart failure severity. The expressions of IGF-1 and IGF-1 receptor proteins were examined in endomyocardial biopsies obtained from other patients with normal or impaired LV function. RESULTS The pericardial 1GF-1 and BNP levels were positively correlated with the plasma BNP level (both p < 0.001). The pericardial IGF-1 level was increased in heart failure patients, whereas the plasma 1GF-1 level was rather decreased. The pericardial IGF-1 level was inversely correlated with the LV ejection fraction (p < 0.001), whereas the plasma 1GF-1 level was not. Positive immunostaining for IGF-1 and 1GF-1 receptor proteins was enhanced in myocardial biopsies from failing hearts compared with those from nonfailing hearts. CONCLUSIONS The pericardial IGF-1 level was increased in patients with LV dysfunction and heart failure, whereas the plasma IGF-1 level was decreased. These results may indicate that up-regulation of the cardiac IGF-1 system serves as a compensatory mechanism for LV dysfiinction.

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