首页> 外文期刊>Annals of laboratory medicine. >Comparison of Quantitation of Cytomegalovirus DNA by Real-Time PCR in Whole Blood with the Cytomegalovirus Antigenemia Assay
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Comparison of Quantitation of Cytomegalovirus DNA by Real-Time PCR in Whole Blood with the Cytomegalovirus Antigenemia Assay

机译:实时荧光定量PCR检测全血中巨细胞病毒DNA与巨细胞病毒抗原测定的比较

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Background: Quantitation of cytomegalovirus (CMV) DNA using real-time PCR has been utilized for monitoring CMV infection. However, the CMV antigenemia assay is still the ‘gold standard’ assay. There are only a few studies in Korea that compared the efficacy of use of real-time PCR for quantitation of CMV DNA in whole blood with the antigenemia assay, and most of these studies have been limited to transplant recipients. Method: 479 whole blood samples from 79 patients, falling under different disease groups, were tested by real-time CMV DNA PCR using the Q-CMV real-time complete kit (Nanogen Advanced Diagnostic S.r.L., Italy) and CMV antigenemia assay (CINA Kit, ArgeneBiosoft, France), and the results were compared. Repeatedly tested patients were selected and their charts were reviewed for ganciclovir therapy. Results: The concordance rate of the two assays was 86.4% (Cohen’s kappa coefficient value=0.659). Quantitative correlation between the two assays was a moderate (r=0.5504, P Conclusions: Q-CMV real-time complete kit is a useful tool for early detection of CMV infection in whole blood samples in transplant recipients.
机译:背景:使用实时荧光定量PCR检测巨细胞病毒(CMV)DNA已用于监测CMV感染。但是,CMV抗原血症检测仍是“金标准”检测。在韩国,只有少数研究比较了使用实时PCR定量全血中CMV DNA和抗原血症测定的功效,而这些研究中的大多数仅限于移植接受者。方法:使用Q-CMV实时完整试剂盒(Nanogen Advanced Diagnostic SrL,意大利)和CMV抗原血症测定法(CINA试剂盒),通过实时CMV DNA PCR检测了来自79个患者的479个全血样品,这些样品属于不同疾病组(法国ArgeneBiosoft)进行比较。选择经过反复测试的患者,并对其图表进行更昔洛韦治疗。结果:两种检测方法的一致性率为86.4%(科恩的kappa系数值= 0.659)。两种测定之间的定量相关性为中等(r = 0.5504,P结论):Q-CMV实时完整试剂盒是早期检测移植受者全血中CMV感染的有用工具。

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