C-reactive protein and coronary artery calcium in asymptomatic women with systemic lupus erythematosus or rheumatoid arthritis

被引:61
作者
Kao, Amy H. [1 ]
Wasko, Mary Chester M. [1 ]
Krishnaswami, Shanthi [4 ]
Wagner, Joseph [5 ]
Edmundowicz, Daniel [2 ]
Shaw, Penny [1 ]
Cunningham, Amy Lynn [6 ]
Danchenko, Natalya [3 ]
Sutton-Tyrrell, Kim [3 ]
Tracy, Russell P. [7 ]
Kuller, Lewis H. [3 ]
Manzi, Susan [1 ,3 ]
机构
[1] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Med, Div Rheumatol & Clin Immunol, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Cardiovasc Inst, Pittsburgh, PA USA
[3] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA USA
[4] Med Coll Wisconsin, Dept Med, Div Endocrinol, Milwaukee, WI 53226 USA
[5] Wright State Univ, Dayton, OH 45435 USA
[6] LaSalle Univ, Dept Psychol, Philadelphia, PA USA
[7] Univ Vermont, Burlington, VT USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.amjcard.2008.04.059
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Patients with systemic lupus erythematosus (SLE) and those with rheumatoid arthritis (RA) have increased risk for atherosclerotic cardiovascular disease. The aims of this study were to compare the presence of coronary artery calcium (CAC) in age- and race-matched women with SLE, those with RA, and healthy controls without diabetes mellitus or history of myocardial infarction, angina pectoris, or stroke and to investigate its relation with traditional risk factors, inflammation, and endothelial activation. Study subjects completed cardiovascular risk factor assessment and electron-beam computed tomography that measured CAC. The 2 patient groups had similar prevalence and extent of CAC as well as significantly increased odds of having any CAC (odds ratio 1.87, 95% confidence interval 1.09 to 3.21) and more extensive CAC (odds ratio 4.04, 95% confidence interval 1.42 to 11.56 for CAC score > 100) compared with healthy controls. After controlling for differences in cardiovascular risk factors, including insulin resistance and hypertension, the results remained statistically significant. After adjustment for differences in levels of C-reactive protein and/or soluble intercellular adhesion molecule-1, however, women with chronic inflammatory diseases no longer had significantly increased odds of having any CAC or more extensive CAC compared with controls. In conclusion, asymptomatic and nondiabetic women with chronic inflammatory diseases had significantly increased odds of having CAC and more extensive CAC compared with age- and race-matched healthy controls. The increased odds for CAC may in part result from higher levels of inflammation and endothelial activation in these patients. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:755 / 760
页数:6
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