Rapid improvement of nitric oxide bioavailability after lipid-lowering therapy with cerivastatin within two weeks

John, Stefan and Delles, Christian and Jacobi, Johannes and Schlaich, Markus P. and Schneider, Markus and Schmitz, Gerd and Schmieder, Roland E. (2001) Rapid improvement of nitric oxide bioavailability after lipid-lowering therapy with cerivastatin within two weeks. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 37 (5). pp. 1351-1358. ISSN 0735-1097, 1558-3597

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Abstract

OBJECTIVES We investigated whether improvement of endothelial dysfunction in hypercholesterolemia can be achieved with short-term lipid-lowering therapy. BACKGROUND Impaired endothelium-dependent vasodilation plays a pivotal role in the pathogenesis of atherosclerosis and acute coronary syndromes. METHODS In a randomized, double-blind, placebo-controlled trial, we studied 37 patients (52 +/- 11 yrs) with low density lipoprotein cholesterol greater than or equal to 160 mg/d1(196 +/- 44 mg/dl) randomly assigned to either cerivastatin (0.4 mg/d) or placebo. Endothelium-dependent vasodilation of the forearm vasculature was measured by plethysmography and intra-arterial infusion of acetylcholine (ACh 12, 48 mug/min) and endothelium-independent vasodilation by intra-arterial infusion of nitroprusside (3.2, 12.8 mug/min). RESULTS Low density lipoprotein cholesterol decreased after two weeks of treatment (cerivastatin -33 +/- 4% vs. placebo +2 +/- 4%, x +/- SEM, p < 0.001). Endothelium-dependent vasodilation improved after two weeks of therapy with cerivastatin compared with baseline (ACh 12 <mu>g/min: +22.3 +/- 5.2 vs. +11.2 +/- 1.9 ml/min/100 ml, p < 0.01; ACh 48 <mu>g/min: +31.2 +/- 6.3 vs, +19.1 +/- 3.1 ml/min/100 ml, p < 0.05). In contrast, changes in forearm blood how to ACh were similar before and after therapy in the placebo group (ACh 12 <mu>g/min: +12.9 +/- 3.6 vs. +9.0 +/- 1.9 ml/min/100 ml, NS; ACh 48 mug/min: +20.7 +/- 3.7 vs. 19.4 +/- 2.9 ml/min/100 ml, NS). Endothelium-dependent vasodilation improved in comparison with placebo (ACh 48 mug/min: +203 +/- 85% [cerivastatin] vs. -26 +/- 71% [placebo], p < 0.05). This improvement in endothelium-dependent vasodilation was no longer observed when the nitric oxide-synthase inhibitor N(G)-monomethyl-L-arginine was coinfused (ACh 48 <mu>g/min + N(G)-monomethyl-L-arginine 4 mu mol/min -48 +/- 85% [cerivastatin]). CONCLUSIONS Short-term lipid-lowering therapy with cerivastatin can improve endothelial function and NO bioavailability after two weeks in patients with hypercholesterolemia. (J Am Coll Cardiol 2001;37:1351-8) (C) 2001 by the American College of Cardiology.

Item Type: Article
Uncontrolled Keywords: CORONARY-ARTERY DISEASE; SINGLE LDL APHERESIS; ENDOTHELIAL FUNCTION; HYPERCHOLESTEROLEMIC PATIENTS; DEPENDENT VASODILATATION; CHOLESTEROL REDUCTION; ANGIOTENSIN-II; ATHEROSCLEROSIS; SYNTHASE; HUMANS;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin
Depositing User: Dr. Gernot Deinzer
Date Deposited: 07 Feb 2022 14:48
Last Modified: 07 Feb 2022 14:48
URI: https://pred.uni-regensburg.de/id/eprint/41597

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