Oh Ae-Chin, Kim Heyjin, Lee Jin-Kyung, Hong Young-Jun
Clin Lab. 2023 Oct 1;69(10). doi: 10.7754/Clin.Lab.2023.230546.
COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), can be diagnosed using rapid real-time PCR, real-time reverse transcription PCR (rRT-PCR), or rapid antigen testing. Among these, rRT-PCR is considered the gold standard assay. The Xpert Xpress SARS-CoV-2 assay is a rapid real-time PCR test, approved by the Korean Disease Control and Prevention Agency in 2020. The overall concordance and positive concordance rates of the Xpert assay with the STANDARD M nCoV Real-Time Detection kit were determined.
All samples with positive or inconclusive Xpert test results from July 2021 to February 2023 that underwent confirmatory testing using the reference rRT-PCR assay were included in the analysis.
Samples from 224 patients (93 men and 131 women) with a median age of 59 years (range 15 - 90 years) were included. Of 212 samples that tested positive using Xpert, 112 (52.8%) were true positves and 100 (47.2%) were false positives on rRT-PCR testing. The overall concordance and positive concordance rates were 52.8% (112/212) and 54.5% (112/224), respectively. In the Xpert positive group, the samples had a lower Ct value for the E gene than the N2 gene. The Ct values for the E and N2 genes were significantly lower in the positive group than in the inconclusive group.
Positive or inconclusive Xpert results should be confirmed by the gold standard rRT-PCR for early control of this disease. Furthermore, Korea's policy should be reconsidered given the high false-positive rate of the rapid real-time PCR Xpert Xpress SARS-CoV-2 assay.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)可通过快速实时聚合酶链反应(PCR)、实时逆转录PCR(rRT-PCR)或快速抗原检测进行诊断。其中,rRT-PCR被认为是金标准检测方法。Xpert Xpress SARS-CoV-2检测是一种快速实时PCR检测,于2020年获得韩国疾病控制与预防机构批准。测定了Xpert检测与标准M nCoV实时检测试剂盒的总体一致性率和阳性一致性率。
纳入2021年7月至2023年2月期间Xpert检测结果为阳性或不确定且使用参考rRT-PCR检测进行确证检测的所有样本进行分析。
纳入了224例患者(93例男性和131例女性)的样本,中位年龄为59岁(范围15 - 90岁)。在212份Xpert检测呈阳性的样本中,rRT-PCR检测有112份(52.8%)为真阳性,100份(47.2%)为假阳性。总体一致性率和阳性一致性率分别为52.8%(112/212)和54.5%(112/224)。在Xpert阳性组中,样本E基因的Ct值低于N2基因。阳性组中E和N2基因的Ct值显著低于不确定组。
对于该疾病的早期防控,Xpert检测结果为阳性或不确定时,应以金标准rRT-PCR进行确证。此外,鉴于快速实时PCR Xpert Xpress SARS-CoV-2检测的高假阳性率,韩国的相关政策应重新考虑。