Heart-type fatty acid-binding protein (H-FABP), a marker of acute myocardial infarction and a soluble cytosolic protein, may be released following left ventricular remodelling in cardiac overloaded hearts caused by hypertension, aortic regurgitation (AR) or aortic stenosis (AS). Our aim was to investigate if H-FABP levels are associated with left ventricular remodelling and clinical outcome in hypertensive patients with AR or AS. H-FABP and brain natriuretic peptide (BNP) were measured, glomerular filtration rate (GFR) was estimated using the modification of diet in renal disease (MDRD) equation, and left ventricular dimension at systole corrected for body surface area (LVDs/BSA) and relative wall thickness (RWT) were determined by echocardiography in hypertensive patients with mild-to-moderate AR (n ¼ 78), those with mild-to-moderate AS (n ¼ 73) and those without valvular heart diseases (HT) (n ¼ 50).H-FABP levels were significantly higher in AR (4.973 ng/ml) and in AS (4.573) than in HT (3.471) and BNP (65773 pg/ml, 76775, 35722). H-FABP correlated with LVDs/BSA in AR (b ¼ 0.23, Po0.05), and RWT in AS (b ¼ 0.18, Po0.05) after adjustment for age, gender and all the other variables. AS and AR patients were prospectively followed up for cardiac events during 34719 months. A multivariate Cox hazard analysis indicated H-FABP was an independent predictor of outcome both in AR (relative risk (RR) ¼ 7.61, 95% CI ¼ 2.39-25.3) and AS (RR ¼ 13.6, 95% CI ¼ 3.27-66.9). H-FABP, associated with left ventricular remodelling, is useful in predicting clinical outcome in hypertensive patients with mild-to-moderate aortic valve diseases.