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Rosuvastatin affecting aortic valve endothelium to slow the progression of aortic stenosis.

作者信息

Moura Luis M, Ramos Sandra F, Zamorano José L, Barros Isabel M, Azevedo Luis F, Rocha-Gonçalves Francisco, Rajamannan Nalini M

机构信息

Hospital Pedro Hispano, Matosinhos, Portugal.

出版信息

J Am Coll Cardiol. 2007 Feb 6;49(5):554-61. doi: 10.1016/j.jacc.2006.07.072. Epub 2007 Jan 22.


DOI:10.1016/j.jacc.2006.07.072
PMID:17276178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3951859/
Abstract

OBJECTIVES: The objective of this study was to test the effect of a 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase inhibitor on the progression of moderate to severe aortic stenosis as measured by echocardiography. BACKGROUND: Recent retrospective studies support the hypothesis that statins slow the progression of aortic stenosis. METHODS: We performed an open-label, prospective study evaluating 121 consecutive patients with asymptomatic moderate to severe aortic stenosis (aortic valve area > or = 1.0 cm2; mean age 73.7 +/- 8.9 years; 57 men and 64 women), treated with and without rosuvastatin according to the National Cholesterol Education Program Adult Treatment Panel III guidelines. Echocardiographic, serum lipid, and inflammatory markers were measured at baseline and every 6 months for 18 months. RESULTS: Sixty-one patients (50.4%) with elevated LDL (159.7 +/- 33.4 mg/dl), aortic valve velocity (3.65 +/- 0.64 m/s), and aortic valve area (1.23 +/- 0.42 cm2) received rosuvastatin (20 mg/day), and 60 (49.6%) with a normal LDL (118.6 +/- 37.4 mg/dl), aortic valve velocity (3.62 +/- 0.61 m/s), and aortic valve area (1.20 +/- 0.35 cm2) received no statin. During a mean follow-up of 73 +/- 24 weeks, the change in aortic valve area in the control group was -0.10 +/- 0.09 cm2/year versus -0.05 +/- 0.12 cm2/year in the rosuvastatin group (p = 0.041). The increase in aortic valve velocity was 0.24 +/- 0.30 m/s/year in the control group and 0.04 +/- 0.38 m/s/year in the rosuvastatin group (p = 0.007). There was significant improvement in serum lipid and echocardiographic measures of aortic stenosis in the statin group. CONCLUSIONS: Prospective treatment of aortic stenosis with rosuvastatin by targeting serum LDL slowed the hemodynamic progression of aortic stenosis. This is the first prospective study that shows a positive effect of statin therapy for this disease process. (Rosuvastatin Affecting Aortic Valve Endothelium; http://www.clinicaltrials.gov/ct/show/NCT00114491?order = 1; NCT0014491).

摘要

相似文献

[1]
Rosuvastatin affecting aortic valve endothelium to slow the progression of aortic stenosis.

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[6]
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[4]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Human degenerative valve disease is associated with up-regulation of low-density lipoprotein receptor-related protein 5 receptor-mediated bone formation.

J Am Coll Cardiol. 2006-4-18

[2]
Effect of very high-intensity statin therapy on regression of coronary atherosclerosis: the ASTEROID trial.

JAMA. 2006-4-5

[3]
Relation of circulating C-reactive protein to progression of aortic valve stenosis.

Am J Cardiol. 2006-1-1

[4]
Atorvastatin inhibits hypercholesterolemia-induced calcification in the aortic valves via the Lrp5 receptor pathway.

Circulation. 2005-8-30

[5]
A randomized trial of intensive lipid-lowering therapy in calcific aortic stenosis.

N Engl J Med. 2005-6-9

[6]
Atorvastatin inhibits calcification and enhances nitric oxide synthase production in the hypercholesterolaemic aortic valve.

Heart. 2005-6

[7]
Angiotensin-converting enzyme inhibitors and change in aortic valve calcium.

Arch Intern Med. 2005-4-25

[8]
Msx2 promotes cardiovascular calcification by activating paracrine Wnt signals.

J Clin Invest. 2005-5

[9]
Frequency by decades of unicuspid, bicuspid, and tricuspid aortic valves in adults having isolated aortic valve replacement for aortic stenosis, with or without associated aortic regurgitation.

Circulation. 2005-2-22

[10]
Statins but not angiotensin-converting enzyme inhibitors delay progression of aortic stenosis.

Circulation. 2004-9-7

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