Pleiotropic Effects With Equivalent Low-density Lipoprotein Cholesterol Reduction: Comparative Study Between Simvastatin and Simvastatin/Ezetimibe Coadministration


Autoria(s): ARAUJO, Daniel B.; BERTOLAMI, Marcelo C.; FERREIRA, Waldinai P.; ABDALLA, Dulcineia S. P.; FALUDI, Andre A.; NAKAMURA, Yara; BRICHARELLO, Liliana P.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Background: Coadministration of any statin with ezetimibe is as effective as using high doses of the same statin in the reduction Of tow-density lipoprotein cholesterol (LDL-c). There may be other effects called pleiotropics. Objective: To compare the effectiveness of 2 different treatments that obtain equivalent LDL-c reductions (80 mg of simvastatin, once a clay and coadministration of 10 mg of simvastatin and 10 mg of ezetimibe, once a day) over endothelial function and inflammation. Methods: Twenty-three randomized patients with hypercholesterolemia in a 2 X 2 crossover protocol were Studied. Endothelial function was analyzed by ultrasound assessment of endothelial dependent flow-mediated vasodilation of the brachial artery, and inflammation was estimated by high-sensitivity C-reactive protein (hs-CRP). Results: LDL-c reduction was similar between the 2 treatments with simvastatin/ezetimibe and with simvastatin (P < 0.001); no difference between treatments was found (P = 0.968). Both treatments improved significantly the endothelial function [3.61% with simvastatin/ezetimibe (P = 0.003) and 5.08%. with simvastatin (P < 0.001)]; no difference was found between the 2 treatments (P = 0.291). hs-CRP had a 23% reduction with simvastatin/ezetimibe (P = 0.004) and a 30% reduction with simvastatin alone (P = 0.01), with no significant difference between the 2 treatments (P = 0.380). Conclusion: The 2 forms of treatment presented similar pleiotropic effects: improvement in endothelial function and decrease in hsCRP levels.

Merck Sharp and Dohme

Astra-Zeneca

Pfizer

Schering-Plough

Bayer

Identificador

JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, v.55, n.1, p.1-5, 2010

0160-2446

http://producao.usp.br/handle/BDPI/19591

http://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000274172000001&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecord

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

Relação

Journal of Cardiovascular Pharmacology

Direitos

restrictedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #hypercholesterolemia #C-reactive protein #endothelium #CORONARY-HEART-DISEASE #C-REACTIVE PROTEIN #PRIMARY HYPERCHOLESTEROLEMIA #ENDOTHELIAL FUNCTION #ABSORPTION INHIBITOR #DOSE ATORVASTATIN #STATIN THERAPY #DOUBLE-BLIND #EZETIMIBE #EFFICACY #Cardiac & Cardiovascular Systems #Pharmacology & Pharmacy
Tipo

article

original article

publishedVersion