首页> 外文期刊>Journal of Clinical Microbiology >Prospective Evaluation of the Hybrid Capture 2 and AMPLICOR Human Papillomavirus (HPV) Tests for Detection of 13 High-Risk HPV Genotypes in Atypical Squamous Cells of Uncertain Significance
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Prospective Evaluation of the Hybrid Capture 2 and AMPLICOR Human Papillomavirus (HPV) Tests for Detection of 13 High-Risk HPV Genotypes in Atypical Squamous Cells of Uncertain Significance

机译:杂种捕获2和AMPLICOR人乳头瘤病毒(HPV)测试用于检测非典型鳞状细胞中13种高危型HPV基因型的前瞻性评估不确定性

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The use of high-risk human papillomavirus (hrHPV) testing as an adjunct to cervical cytology in population-based screening programs is currently based on DNA hybridization and PCR assays. The aim of this study was to prospectively assess the diagnostic performance of the Hybrid Capture 2 test (HC2; Digene Corporation) in comparison with that of the recently developed PCR-based AMPLICOR HPV test (Roche Molecular Systems) for the detection of 13 hrHPV types. A reverse line blot hybridization assay (Innogenetics) was used as an internal reference standard in discordant cases. Two hundred seventy-one patients with atypical squamous cells of uncertain significance (ASCUS) in cervical samples underwent hrHPV testing. The chi-square test was performed to compare respective proportions. Totals of 160/271 (59%) and 156/271 (58%) were found to be positive for hrHPV with HC2 and AMPLICOR, respectively. Concordant results were obtained for 235 (86.7%) of the 271 samples (kappa statistic, 0.73 ± 0.04). Considering types 26, 53, and 66 as oncogenic types, negative predictive values (NPVs) of HC2 and AMPLICOR were 92.8% and 87.8%, respectively (difference was not significant), and their respective accuracies were 94.8% and 91.9% (difference was not significant). Considering types 26, 53, and 66 as not oncogenic, the respective HC2 and AMPLICOR NPVs were 92.8% and 97.4% (difference was not significant), and accuracy was significantly higher for the AMPLICOR assay (95.9% versus 90.8% for HC2) (P < 0.05). For ASCUS samples, the NPV was 92.8% for HC2 testing and might be compromised if the copy number of HPV DNA was low. The NPV was 97.4% for the AMPLICOR assay and might be compromised if HPV types 26, 53, and 66 were considered oncogenic. The accuracy of these two assays is good and is compatible with routine clinical use in the triage of ASCUS cases.
机译:在基于人群的筛查计划中,高风险人乳头瘤病毒(hrHPV)检测作为宫颈细胞学检查的辅助手段目前基于DNA杂交和PCR分析。这项研究的目的是与最近开发的基于PCR的AMPLICOR HPV测试(Roche Molecular Systems)用于检测13种hrHPV类型的结果相比,前瞻性地评估Hybrid Capture 2测试(HC2; Digene Corporation)的诊断性能。 。在不一致的情况下,将反向线杂交实验(Innogenetics)用作内部参考标准。 hrHPV测试对211例宫颈样本中具有不确定意义的非典型鳞状细胞(ASCUS)的患者进行了检查。进行卡方检验以比较各个比例。发现分别含HC2和AMPLICOR的hrHPV阳性的总数为160/271(59%)和156/271(58%)。对271个样本中的235个(86.7%)获得了一致的结果(k统计值,0.73±0.04)。以26、53和66型为致癌类型,HC2和AMPLICOR的阴性预测值(NPVs)分别为92.8%和87.8%(差异不显着),其各自的准确度分别为94.8%和91.9%(差异不重要)。考虑到26、53和66型非致癌性,HC2和AMPLICOR的NPV分别为92.8%和97.4%(差异不显着),并且AMPLICOR分析的准确度明显更高(HC2的准确率分别为95.9%和90.8%)( P <0.05)。对于ASCUS样品,HC2检测的NPV为92.8%,如果HPV DNA的拷贝数低,则NPV可能会受到影响。 AMPLICOR分析的NPV为97.4%,如果HPV 26、53和66型被认为是致癌的,则可能会受到损害。这两种测定法的准确性很好,并且与ASCUS病例分诊中的常规临床使用兼容。

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