arterial hypertension;
hypertrophy;
echocardiography;
high density lipoprotein-cholesterol;
D O I:
10.1097/00004872-200112000-00021
中图分类号:
R6 [外科学];
学科分类号:
1002 ;
100210 ;
摘要:
Objective The proportion of left ventricular (LV) mass variability explained by blood pressure in essential hypertension is small, and several non-haemodynamic determinants of LV mass have been identified or hypothesized. This study examines the possible relation between blood lipids and LV mass in hypertension. Design Never-treated non-diabetic hypertensive patients. Setting Hospital hypertension outpatient clinics in Umbria, Italy. Patients We investigated the association between high-density lipoprotein (HDL)-cholesterol and echocardiographic LV mass in 1306 never-treated subjects with essential hypertension. Subjects with previous cardiovascular events, diabetes and current or previous antihypertensive or lipid-lowering therapy were excluded. Results HDL-cholesterol showed an inverse association with LV mass (r = -0.30, P < 0.001). No association was found between LV mass and total or low-density lipoprotein cholesterol. With multiple linear regression analysis we tested the independent contribution of several potential determinants of LV mass in women and in men. Average 24 h blood pressure (both pulse and mean), body mass index, height(2.7), stroke volume, age (all P < 0.01) and low HDL-cholesterol (P < 0.0001 in women, P < 0.001 in men) were associated with a greater LV mass in both sexes. Triglycerides showed a weak univariate association with LV mass in women (r = 0.11, P < 0.02), which did not hold in a multivariate analysis. Conclusions Low HDL-cholesterol is an independent predictor of LV mass in untreated hypertensive subjects. Common hormonal and metabolic mechanisms, including insulin resistance, could explain this association, which may contribute to the adverse prognostic significance of low HDL-cholesterol levels. J Hypertens 19:2265-2270 (C) 2001 Lippincott Williams & Wilkins.
机构:
Univ London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, EnglandUniv London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, England
Brett, SE
;
Ritter, JM
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机构:
Univ London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, EnglandUniv London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, England
Ritter, JM
;
Chowienczyk, PJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, EnglandUniv London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, England
机构:
Univ London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, EnglandUniv London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, England
Brett, SE
;
Ritter, JM
论文数: 0引用数: 0
h-index: 0
机构:
Univ London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, EnglandUniv London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, England
Ritter, JM
;
Chowienczyk, PJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, EnglandUniv London Kings Coll, Dept Clin Pharmacol, Ctr Cardiovasc Biol & Med, St Thomas Hosp, London SE1 7EH, England