Literature DB >> 17010800

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

Naoki Abe1, Toshiro Matsunaga, Kunihiko Kameda, Hirofumi Tomita, Takayuki Fujiwara, Hiroshi Ishizaka, Hiroyuki Hanada, Kozo Fukui, Ikuo Fukuda, Tomohiro Osanai, Ken Okumura.   

Abstract

OBJECTIVES: To test the hypothesis that the cardiac insulin-like growth factor-1 (IGF-1) system is up-regulated in the failing heart, we measured the pericardial (cardiac) and plasma (circulating) IGF-1 levels in coronary artery disease patients.
BACKGROUND: Local IGF-1 systems are regulated differently from the systemic IGF-1 system. The cardiac IGF-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 IGF-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 IGF-1 level was rather decreased. The pericardial IGF-1 level was inversely correlated with the LV ejection fraction (p < 0.001), whereas the plasma IGF-1 level was not. Positive immunostaining for IGF-1 and IGF-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 dysfunction.

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Year:  2006        PMID: 17010800     DOI: 10.1016/j.jacc.2006.06.048

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  4 in total

1.  Molecular signature of a right heart failure program in chronic severe pulmonary hypertension.

Authors:  Jennifer I Drake; Herman J Bogaard; Shiro Mizuno; Berrick Clifton; Bin Xie; Yuan Gao; Catherine I Dumur; Paul Fawcett; Norbert F Voelkel; Ramesh Natarajan
Journal:  Am J Respir Cell Mol Biol       Date:  2011-06-30       Impact factor: 6.914

2.  The impact of IGF-I gene polymorphisms on coronary artery disease susceptibility.

Authors:  Hsiu-Ling Lin; Kwo-Chang Ueng; Hsiang-Ling Wang; Tsung-Po Chen; Shun-Fa Yang; Shu-Chen Chu; Yih-Shou Hsieh
Journal:  J Clin Lab Anal       Date:  2013-02-19       Impact factor: 2.352

3.  Biventricular differences in β-adrenergic receptor signaling following burn injury.

Authors:  Ashley N Guillory; Robert P Clayton; Anesh Prasai; Amina El Ayadi; David N Herndon; Celeste C Finnerty
Journal:  PLoS One       Date:  2017-12-12       Impact factor: 3.240

4.  MicroRNA profiling of pericardial fluid samples from patients with heart failure.

Authors:  Suvi M Kuosmanen; Juha Hartikainen; Mikko Hippeläinen; Hannu Kokki; Anna-Liisa Levonen; Pasi Tavi
Journal:  PLoS One       Date:  2015-03-12       Impact factor: 3.240

  4 in total

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