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无症状巨细胞病毒血症与晚期HIV感染患者血清淀粉样蛋白A水平升高有关。

Aymptomatic CMV viremia is associated with increased levels of serum amyloid A in patients with advanced HIV-infection.

作者信息

Steininger Christoph, Graninger W, Zoufaly A, Zöllner B, Feucht H-H, Kundi M, Stahmer I, Stellbrink H-J, van Lunzen J

机构信息

Medical University of Vienna, Department of Medicine I, Währinger Gürtel 18-20, A-1090 Vienna, Austria.

出版信息

Eur J Med Res. 2008 Jun 24;13(6):304-8.

Abstract

OBJECTIVE

We evaluated assays for the measurement of acute phase protein levels in plasma for their usefulness to identify sensitively an inflammatory response to active cytomegalovirus CMV infection in HIV-infected patients.

METHODS

Plasma samples were collected from 28 CMV-seropositive patients with advanced HIV-infection (CD4-cell count <200/microl) before commencement of antiretroviral therapy. Sensitivity, specificity, and area under receiver operating characteristic curve for the selected acute phase protein assays (haptoglobin, fibronectin, high-sensitivity C-reactive protein (hs-CRP), human interleukin-6, serum amyloid A (SAA), and human lipopolysacharide binding protein) were compared with results of a CMV-specific PCR assay.

RESULTS

CMV viremia was detectable in 8/28 patients. Levels of SAA correlated well with those of hs-CRP (r' = 0.439, P = 0.019 (Spearman rank correlation)). Levels of SAA >3 mg/L discriminated with 100% sensitivity and 40% specificity between HIV-infected patients with and without active CMV infection. Sensitivity of fibronectin was 100% and specificity 15% at a threshold-value corresponding with the lower limit of normal values as defined by the manufacturer of the assay (>29 mg/dL). Levels of the other acute phase proteins evaluated did not correlate with detection of CMV-DNA in plasma.

CONCLUSION

Increased levels of SAA indicate sensitively an inflammatory response to active CMV infection. Use of a CMV-specific virological assay is required to confirm the specificity of a high SAA-level but may be limited to samples with high SAA-levels. Hence, screening for increased levels of SAA in patients with advanced HIV-infection may allow early identification of active CMV infection.

摘要

目的

我们评估了用于测量血浆中急性期蛋白水平的检测方法,以确定其在灵敏识别HIV感染患者对活动性巨细胞病毒(CMV)感染的炎症反应方面的实用性。

方法

在抗逆转录病毒治疗开始前,从28例晚期HIV感染(CD4细胞计数<200/μl)且CMV血清学阳性的患者中采集血浆样本。将所选急性期蛋白检测方法(触珠蛋白、纤连蛋白、高敏C反应蛋白(hs-CRP)、人白细胞介素-6、血清淀粉样蛋白A(SAA)和人脂多糖结合蛋白)的敏感性、特异性和受试者操作特征曲线下面积与CMV特异性PCR检测结果进行比较。

结果

28例患者中有8例可检测到CMV病毒血症。SAA水平与hs-CRP水平相关性良好(r' = 0.439,P = 0.019(Spearman等级相关性))。SAA>3 mg/L时,在有和无活动性CMV感染的HIV感染患者之间的鉴别敏感性为100%,特异性为40%。在与检测方法制造商定义的正常下限相对应的阈值(>29 mg/dL)下,纤连蛋白的敏感性为100%,特异性为15%。所评估的其他急性期蛋白水平与血浆中CMV-DNA的检测不相关。

结论

SAA水平升高灵敏地表明对活动性CMV感染有炎症反应。需要使用CMV特异性病毒学检测来确认高SAA水平的特异性,但可能仅限于SAA水平高的样本。因此,对晚期HIV感染患者筛查SAA水平升高可能有助于早期识别活动性CMV感染。

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