Statin withdrawal: Clinical implications and molecular mechanisms

被引:49
作者
Cubeddu, Luigi X.
Seamon, Matthew J.
机构
[1] Nova SE Univ, Coll Pharm, Dept Pharmaceut Sci, Hlth Profess Div, Ft Lauderdale, FL 33328 USA
[2] Nova SE Univ, Coll Pharm, Dept Adm Sci, Hlth Profess Div, Ft Lauderdale, FL 33328 USA
[3] Nova SE Univ, Coll Pharm, Dept Pharm Practice, Hlth Profess Div, Ft Lauderdale, FL 33328 USA
来源
PHARMACOTHERAPY | 2006年 / 26卷 / 09期
关键词
statins; statin withdrawal; cardiovascular risk; 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors; HMG-CoA reductase inhibitors;
D O I
10.1592/phco.26.9.1288
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Retrospective analyses of data from the Platelet Receptor Inhibition in Ischemic Syndrome Management (PRISM), the National Registry of Myocardial Infarction 4, and the Global Registry of Acute Coronary Events (GRACE) trials revealed that the benefits of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) on acute coronary outcomes are rapidly lost and outcomes worsened if statins are discontinued during a patient's hospitalization for an acute coronary syndrome. Withdrawal of statin therapy, in the first 24 hours of hospitalization for non-ST-elevation myocardial infarction increased the hospital morbidity and mortality rate versus continued therapy (11.9% vs; 5.7%, p < 0.01). Data from the Treating New Targets (TNT) study, however, suggested that short-term discontinuation of statin therapy in patients with stable cardiac conditions may not substantially increase the risk of acute coronary syndromes. In patients with acute coronary syndromes who discontinue statins, the rapid increase in risk of an event may result not only from the lost benefits from the therapy, but also from rebound inhibition of vascular protective substances and activation of vascular deleterious substances. Statins inhibit cholesterol synthesis in vascular cells. By reducing levels of isoprenoid intermediates, statins increase the production of nitric oxide and downregulate angiotensin 11 AT, receptors, endothelin-1, vascular inflammatory adhesion molecules, and inflammatory cytokines. These benefits are rapidly lost and often transiently reversed when statins are acutely discontinued. Acute removal of pleiotropic effects and rebound vascular dysfunction may be more important in an acute coronary event, where inflammation promotes rupture of atherosclerotic plaques and inflammatory and prothrombosis markers are present in high concentration, than in stable chronic vascular disease. In the absence of data from randomized controlled trials, current information suggests that statin therapy should. be continued, and possibly boosted, during hospitalization for an acute coronary syndrome. Because statins are discontinued during the early hospitalization of many patients, practitioners must ensure that statins are not omitted, unless contraindicated, from the treatment of patients with acute coronary syndromes.
引用
收藏
页码:1288 / 1296
页数:9
相关论文
共 48 条
[1]   3-Hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors, atorvastatin and simvastatin, induce apoptosis of vascular smooth muscle cells by downregulation of Bcl-2 expression and Rho A prenylation [J].
Blanco-Colio, LM ;
Villa, A ;
Ortego, M ;
Hernández-Presa, MA ;
Pascual, A ;
Plaza, JJ ;
Egido, J .
ATHEROSCLEROSIS, 2002, 161 (01) :17-26
[2]   Withdrawal of cerivastatin induces monocyte chemoattractant protein 1 and tissue factor expression in cultured vascular smooth muscle cells [J].
Brandes, RP ;
Beer, S ;
Ha, T ;
Busse, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (10) :1794-1800
[3]   Treating dyslipidemia with statins: The risk-benefit profile [J].
Clark, LT .
AMERICAN HEART JOURNAL, 2003, 145 (03) :387-396
[4]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[5]   Vastatins inhibit tissue factor in cultured human macrophages - A novel mechanism of protection against atherothrombosis [J].
Colli, S ;
Eligini, S ;
Lalli, M ;
Camera, M ;
Paoletti, R ;
Tremoli, E .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (02) :265-272
[7]   Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels - Results of AFCAPS/TexCAPS [J].
Downs, JR ;
Clearfield, M ;
Weis, S ;
Whitney, E ;
Shapiro, DR ;
Beere, PA ;
Langendorfer, A ;
Stein, EA ;
Kruyer, W ;
Gotto, AM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (20) :1615-1622
[8]   Effects of statins on endothelium and signaling mechanisms [J].
Endres, M ;
Laufs, U .
STROKE, 2004, 35 (11) :2708-2711
[9]  
Farmer J A, 1996, Adv Pharmacol, V35, P79, DOI 10.1016/S1054-3589(08)60275-6
[10]  
FUHRMANS V, 2002, WALL STREET J 0121, pA10