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首页> 外文期刊>European journal of clinical microbiology and infectious diseases: Official publication of the European Society of Clinical Microbiology >Real-time quantitative PCR analysis of endoscopic biopsies for diagnosing CMV gastrointestinal disease in non-HIV immunocompromised patients: a diagnostic accuracy study
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Real-time quantitative PCR analysis of endoscopic biopsies for diagnosing CMV gastrointestinal disease in non-HIV immunocompromised patients: a diagnostic accuracy study

机译:用于诊断CMV胃肠疾病的内镜活组织检查中的实时定量PCR分析,非HIV免疫疗效患者:诊断准确性研究

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摘要

Cytomegalovirus gastrointestinal diseases (CMV-GIDs) are end-organ diseases of the gastrointestinal (GI) tract caused by CMV in immunocompromised patients. We aimed to evaluate the performance of quantitative polymerase chain reaction (qPCR) on endoscopic biopsies. We retrospectively reviewed the qPCR data on endoscopic biopsies in nonhuman immunodeficiency virus (HIV) immunocompromised patients between January 2009 and May 2015. The performance of the qPCR for CMV-GID was evaluated with the sensitivity, specificity, and area under the receiver operating characteristic curve (AUROC). A total of 195 patients were included, and 28 patients with confirmed CMV-GID were identified. The AUROC of the qPCR was 0.935 (95% confidence interval [CI], 0.885 to 0.985), the sensitivity was 89.3% (95% CI, 71.8 to 97.7%), and the specificity was 85.6% (95% CI, 79.4 to 97.6%) with a cutoff value of 180 copies/g DNA. The proportion of patients with inflammatory bowel disease in the histopathology-negative, PCR-positive group was smaller than that in the histopathology-positive group (10.7 vs 35.0%, p=0.026), but other characteristics were not significantly different. The use of qPCR on endoscopic biopsies demonstrated good diagnostic performance for detecting CMV in non-HIV immunocompromised patients. It may increase the diagnostic yield when combined with a conventional histopathology.
机译:Cytomegalovirus胃肠疾病(CMV-GID)是由CMV在免疫疗效中引起的胃肠道(GI)疾病的终端器官疾病。我们旨在评估定量聚合酶链反应(QPCR)对内窥镜活组织检查的性能。我们回顾性地审查了2009年1月至2015年5月在2009年1月至2015年5月之间的非人免疫缺陷病毒(HIV)免疫缺陷患者内窥镜活检的QPCR数据。CMV-GID的QPCR对接收器操作特性曲线下的敏感性,特异性和面积进行了评估的性能(奥克约)。共用了195名患者,鉴定了28例确诊的CMV-GID患者。 QPCR的氧化氢酮为0.935(95%置信区间[CI],0.885至0.985),敏感性为89.3%(95%CI,71.8至97.7%),特异性为85.6%(95%CI,79.4至79.4)。 97.6%)截止值180拷贝/ g DNA。组织病理学阴性PCR阳性患者炎症性肠病患者的比例小于组织病理学阳性阳性基团(10.7 Vs 35.0%,P = 0.026),但其他特征没有显着差异。在内窥镜活检中使用QPCR证明了检测非HIV免疫性患者中CMV的良好诊断性能。当与常规组织病理学结合时,它可能会增加诊断产量。

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