Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2957296 | Journal of the American Society of Hypertension | 2010 | 7 Pages |
Abstract
Angiotensin II influences development of left ventricular hypertrophy (LVH) by stimulating cardiomyocyte hypertrophy, fibroblast proliferation, and collagen synthesis. Because pro-fibrotic actions of angiotensin may be mediated by increased production of transforming growth factor-β1 (TGF-β1), we assessed whether serum TGF-β1 levels might reflect involvement in LVH development. We analyzed relationships between left ventricular mass and levels of renin, aldosterone, and TGF-β1 in 67 hypertensive subjects (mean age 64 ± 11.3 years) with electrocardiographic evidence of LVH. Levels were obtained after a 2-week washout of antihypertensive medications; two-dimensional echocardiography was subsequently performed. Linear regression analysis showed a correlation between TGF-β1 and LV mass (r = 0.36, P = .002). This was apparently explained by the correlation between TGF-β1 and left ventricular diastolic internal diameter (r = 0.42, P < .001), because no correlation between TGF-β1 levels and LV wall thickness was found. In multivariate analysis, the correlation between TGF-β1 and internal diameter remained significant (r = 0.39, P = .0014). There were no racial differences in levels of TGF-β1 or left ventricular geometry, and no correlations between age, blood pressure, renin, aldosterone, and left ventricular mass or dimensions. These findings indicate that serum TGF-β1 levels are related to left ventricular structure in hypertensive subjects, suggesting its possible involvement in the process of hypertensive left ventricular remodeling.
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Authors
Jesus L. MD, Vladislav MD, Clive MD, PhD, Steven A. MD,