4.5 Article

C-reactive Protein Is a More Sensitive and Specific Marker for Diagnosing Bacterial Infections in Systemic Lupus Erythematosus Compared to S100A8/A9 and Procalcitonin

期刊

JOURNAL OF RHEUMATOLOGY
卷 39, 期 4, 页码 728-734

出版社

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.111044

关键词

SYSTEMIC LUPUS ERYTHEMATOSUS; INFECTION; C-REACTIVE PROTEIN; S100A8/A9; PROCALCITONIN

资金

  1. Brain Korea 21 project for Ajou University School of Medicine
  2. Ministry for Health, Welfare and Family Affairs, Republic of Korea [A080588]

向作者/读者索取更多资源

Objective. C-reactive protein (CRP), S100A8/A9, and procalcitonin have been suggested as markers of infection in patients with systemic lupus erythematosus (SLE). We investigated the clinical significance of these factors for indication of infection in SLE. Methods. Blood samples were prospectively collected from 34 patients with SLE who had bacterial infections and 39 patients with SLE who had disease flares and no evidence of infection. A second set of serum samples was collected after the infections or flares were resolved. Results. CRP levels of SLE patients with infections were higher than those with flares [5.9 mg/dl (IQR 2.42, 10.53) vs 0.06 mg/dl (IQR 0.03, 0.15), p < 0.001] and decreased after the infection was resolved. S100A8/A9 and procalcitonin levels of SLE patients with infection were also higher [4.69 mu g/ml (IQR 2.25, 12.07) vs 1.07 (IQR 0.49, 3.05) (p < 0.001) and 0 ng/ml (IQR 0-0.38) vs 0 (0-0) (p < 0.001), respectively]; these levels were also reduced once the infection disappeared. In the receiver-operating characteristics analysis of CRP, S100A8/A9, and procalcitonin, the area under the curve was 0.966 (95% CI 0.925-1.007), 0.732 (95% CI 0.61-0.854), and 0.667 (95% CI 0.534-0.799), respectively. CRP indicated the presence of an infection with a sensitivity of 100% and a specificity of 90%, with a cutoff value of 1.35 mg/dl. Conclusion. Our data suggest that CRP is the most sensitive and specific marker for diagnosing bacterial infections in SLE. (First Release Feb 15 2012; J Rheumatol 2012;39:728-34; doi:10.3899/jrheum.111044)

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