4.5 Article

Noncalcified Coronary Plaque in Systemic Lupus Erythematosus

期刊

JOURNAL OF RHEUMATOLOGY
卷 37, 期 3, 页码 579-584

出版社

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.090824

关键词

NONCALCIFIED CORONARY PLAQUE; SYSTEMIC LUPUS ERYTHEMATOSUS

资金

  1. National Institutes of Health (NIH) [AR 43727]
  2. National Center for Research Resources [UL1 RR 025005]
  3. NIH Roadmap for Medical Research

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Objective. To Study noncalcified coronary plaque (NCP) in systemic lupus erythematosus (SLE). Methods. Sixty-four-slice coronary multidetector computed tomography (MDCT) was performed in 39 consecutive patients with SLE. MDCT scans were evaluated semiquantitatively by a radiologist 0 using dedicated software. The presence or absence of NCP in each coronary artery was assessed. Patients with mixed plaque (calcified and noncalcified portions) were included in the NCP group. Results. The patient group was 90% women, 64% Caucasian, 31% African American, 5% others mean age 50.5 +/- 9.6 years. Fifty-four percent (21/39) had NCP. Seventy-six percent (16/21) of those with NCP also had coronary calcium (range 0.7 to 1264.1 Agatston units). In univariate analysis, NCP was associated with age (p = 0.01). current nonsteroidal antiinflammatory drug (NSAID) use (p = 0.04), hormone replacement therapy (p = 0.02), current use Of immunosuppressive drugs (p 0.02), current low serum C3 level (p = 0.07), current physician's global assessment of activity (PGA; p = 0.05), and low-density lipoprotein cholesterol (p = 0.04). NCP was not associated with other risk factors for atherosclerosis, including total serum cholesterol, high sensitivity C-reactive protein, and lipoprotein(a). Conclusion. Unlike coronary calcium, which is not associated with SLE activity measures or with active serologies, NCP is more common in patients with SLE with current, 3-, and 6-month activity by PGA. NCP was also associated with the need for current NSAID or immunosuppressive therapy. NCP is an important part of the total atherosclerotic burden in SLE. (First Release Feb 1 2010; J Rheumatol 2010;37:579-84: doi:10.3899/jrheum.090824)

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