Lupus Atherosclerosis Prevention Study (LAPS)

被引:180
作者
Petri, M. A. [1 ]
Kiani, A. N. [1 ]
Post, W. [1 ]
Christopher-Stine, L. [1 ]
Magder, L. S. [2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21205 USA
[2] Univ Maryland, Baltimore, MD 21201 USA
关键词
C-REACTIVE PROTEIN; CORONARY-ARTERY-DISEASE; LIPID-LOWERING THERAPY; INTIMA-MEDIA THICKNESS; RISK-FACTORS; CARDIOVASCULAR-DISEASE; STATIN THERAPY; ACCELERATED ATHEROSCLEROSIS; MULTIPLE-SCLEROSIS; CONTROLLED-TRIAL;
D O I
10.1136/ard.2010.136762
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Cardiovascular disease is one of the major causes of death in systemic lupus erythematosus (SLE). A study was undertaken to investigate whether treatment with statins would reduce subclinical measures of atherosclerosis over a 2-year period. Methods 200 patients with SLE without clinical cardiovascular disease were randomised to receive atorvastatin 40 mg daily or an identical placebo. At baseline and after 2 years of follow-up, helical CT scanning (for coronary artery calcium) and carotid duplex (for intima media thickness/plaque) were performed. Patients were seen for measures of disease activity at 1 month, 3 months and quarterly thereafter. The primary outcome variable was change in coronary artery calcium. Results At baseline, 43% had coronary artery calcium. At 2 years there was no significant difference between the groups in progression of coronary artery calcium, carotid intima media thickness or carotid plaque. There was no significant difference between the groups in disease activity, measures of inflammation or endothelial cell activation. Conclusion This study provides no evidence that atorvastatin reduces subclinical measures of atherosclerosis or disease activity over 2 years in patients with SLE. In fact, it does not appear to reduce biochemical measures of inflammation. The anti-inflammatory effects of statins observed in the general population were not replicated in this SLE clinical trial.
引用
收藏
页码:760 / 765
页数:6
相关论文
共 46 条
[1]  
Ahmad A, 2000, Tenn Med, V93, P21
[2]   Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study [J].
Albert, MA ;
Danielson, E ;
Rifai, N ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01) :64-70
[3]   Treatment of asymptomatic adults with elevated coronary calcium scores with atorvastatin, vitamin C, and vitamin E - The St. Francis Heart Study Randomized Clinical Trial [J].
Arad, Y ;
Spadaro, LA ;
Roth, M ;
Newstein, D ;
Guerci, AD .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 46 (01) :166-172
[4]   Premature coronary-artery atherosclerosis in systemic lupus erythematosus [J].
Asanuma, Y ;
Oeser, A ;
Shintani, AK ;
Turner, E ;
Olsen, N ;
Fazio, S ;
Linton, MF ;
Raggi, P ;
Stein, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (25) :2407-2415
[5]   REPRODUCIBILITY OF CAROTID VESSEL WALL THICKNESS MEASUREMENTS - THE ROTTERDAM STUDY [J].
BOTS, ML ;
MULDER, PGH ;
HOFMAN, A ;
VANES, GA ;
GROBBEE, DE .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1994, 47 (08) :921-930
[6]   Effect of HMG-Coa reductase inhibitors on coronary artery disease as assessed by electron-beam computed tomography [J].
Callister, TQ ;
Raggi, P ;
Cooil, B ;
Lippolis, NJ ;
Russo, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (27) :1972-1978
[7]   Intensive versus moderate lipid lowering with statins after acute coronary syndromes [J].
Cannon, CP ;
Braunwald, E ;
McCabe, CH ;
Rader, DJ ;
Rouleau, JL ;
Belder, R ;
Joyal, SV ;
Hill, KA ;
Pfeffer, MA ;
Skene, AM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (15) :1495-1504
[8]   A pravastatin dose-escalation study in systemic lupus erythematosus [J].
Costenbader, Karen H. ;
Liang, Matthew H. ;
Chibnik, Lori B. ;
Aizer, Juliet ;
Kwon, Hannah ;
Gall, Victoria ;
Karlson, Elizabeth W. .
RHEUMATOLOGY INTERNATIONAL, 2007, 27 (11) :1071-1077
[9]  
Esdaile JM, 2001, ARTHRITIS RHEUM, V44, P2331, DOI 10.1002/1529-0131(200110)44:10<2331::AID-ART395>3.0.CO
[10]  
2-I