High prevalence of the metabolic syndrome in patients with systemic lupus erythematosus: association with disease characteristics and cardiovascular risk factors

被引:188
作者
Chung, Cecilia P.
Avalos, Ingrid
Oeser, Annette
Gebretsadik, Tebeb
Shintani, Ayumi
Raggi, Paolo
Stein, C. Michael
机构
[1] Vanderbilt Univ, Sch Med, Div Rheumatol, Dept Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Biostat, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37232 USA
[4] Emory Univ, Sch Med, Cardiol Sect, Dept Med, Atlanta, GA 30322 USA
关键词
D O I
10.1136/ard.2006.054973
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The metabolic syndrome is an independent risk factor for ischaemic heart disease. Patients with systemic lupus erythematosus (SLE) have accelerated atherosclerosis; however, there are no controlled studies of the metabolic syndrome in patients with SLE. Objective: To compare the prevalence of the metabolic syndrome in patients with SLE and controls and to evaluate its relationship to other cardiovascular risk factors and inflammation. Methods: 102 patients with SLE and 101 controls were studied. The prevalence of the metabolic syndrome was compared in patients and controls using the National Cholesterol Education Program Adult Treatment Panel III (NCEP) and the World Health Organization (WHO) definitions, and associations with cardiovascular risk factors and lupus characteristics were examined. Results: The metabolic syndrome was present in 32.4% of patients and in 10.9% of controls subjects (p < 0.001) using the WHO definition that requires direct determination of insulin resistance, and in 29.4% of patients with SLE and in 19.8% of controls (p = 0.14) using the NCEP definition. Among patients with SLE, both definitions were significantly associated with higher concentrations of C reactive protein (p = 0.001) and the NCEP definition was significantly associated with higher concentrations of homocysteine (p < 0.001), lipoprotein (a) (p = 0.02) and cholesterol (p = 0.04). Neither lupus disease activity nor damage scores were associated with the metabolic syndrome. Conclusions: Patients with SLE have a higher prevalence of insulin resistance and consequently of the WHO-defined metabolic syndrome than controls. In patients with SLE, the metabolic syndrome was associated with higher levels of inflammation and may provide a link between inflammation and increased cardiovascular risk.
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页码:208 / 214
页数:7
相关论文
共 38 条
[1]   The metabolic syndrome:: A concept hard to define [J].
Aguilar-Salinas, CA ;
Rojas, R ;
Gómez-Pérez, FJ ;
Mehta, R ;
Franco, A ;
Olaiz, G ;
Rull, JA .
ARCHIVES OF MEDICAL RESEARCH, 2005, 36 (03) :223-231
[2]  
[Anonymous], 2001, CATEGORICAL DATA ANA
[3]   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
[4]  
Balkau B, 2002, DIABETES METAB, V28, P364
[5]   DERIVATION OF THE SLEDAI - A DISEASE-ACTIVITY INDEX FOR LUPUS PATIENTS [J].
BOMBARDIER, C ;
GLADMAN, DD ;
UROWITZ, MB ;
CARON, D ;
CHANG, CH .
ARTHRITIS AND RHEUMATISM, 1992, 35 (06) :630-640
[6]   Is oxidative stress the pathogenic mechanism underlying insulin resistance, diabetes, and cardiovascular disease? The common soil hypothesis revisited [J].
Ceriello, A ;
Motz, E .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (05) :816-823
[7]   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
[8]   Effects of atorvastatin on glucose homeostasis, postprandial triglyceride response and C-reactive protein in subjects with impaired fasting glucose [J].
Costa, A ;
Casamitjana, R ;
Casals, E ;
Alvarez, L ;
Morales, J ;
Masramón, X ;
Hernández, G ;
Gomis, R ;
Conget, I .
DIABETIC MEDICINE, 2003, 20 (09) :743-745
[9]   Abnormal capillary permeability and endothelial dysfunction in hypertension with comorbid Metabolic Syndrome [J].
Dell'Omo, G ;
Penno, G ;
Pucci, L ;
Mariani, M ;
Del Prato, S ;
Pedrinelli, R .
ATHEROSCLEROSIS, 2004, 172 (02) :383-389
[10]  
El Magadmi M, 2006, J RHEUMATOL, V33, P50