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Validation of a DNA methylation HPV triage classifier in a screening sample

机译:筛选样品中DNA甲基化HPV分类分类的验证

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摘要

High-risk human papillomavirus (hrHPV) DNA tests have excellent sensitivity for detection of cervical intraepithelial neoplasia 2 or higher (CIN2+). A drawback of hrHPV screening, however, is modest specificity. Therefore, hrHPV-positive women might need triage to reduce adverse events and costs associated with unnecessary colposcopy. We compared the performance of HPV16/18 genotyping with a predefined DNA methylation triage test (S5) based on target regions of the human gene EPB41L3, and viral late gene regions of HPV16, HPV18, HPV31 and HPV33. Assays were run using exfoliated cervical specimens from 710 women attending routine screening, of whom 38 were diagnosed with CIN2+ within a year after triage to colposcopy based on cytology and 341 were hrHPV positive. Sensitivity and specificity of the investigated triage methods were compared by McNemar's test. At the predefined cutoff, S5 showed better sensitivity than HPV16/18 genotyping (74% vs 54%, P = 0.04) in identifying CIN2+ in hrHPV-positive women, and similar specificity (65% vs 71%, P = 0.07). When the S5 cutoff was altered to allow equal sensitivity to that of genotyping, a significantly higher specificity of 91% was reached (P < 0.0001). Thus, a DNA methylation test for the triage of hrHPV-positive women on original screening specimens might be a valid approach with better performance than genotyping.
机译:高危人乳头瘤病毒(hrHPV)DNA检测对于检测宫颈上皮内瘤样变2或更高(CIN2 +)具有极高的灵敏度。 hrHPV筛查的缺点是特异性中等。因此,hrHPV阳性的妇女可能需要分流以减少不良事件和不必要的阴道镜检查所带来的费用。我们将HPV16 / 18基因分型的性能与基于人类基因EPB41L3的目标区域以及HPV16,HPV18,HPV31和HPV33的病毒晚期基因区域的预定义DNA甲基化分类测试(S5)进行了比较。使用来自710例接受常规筛查的妇女的脱落宫颈样本进行分析,其中38例在根据细胞学分流术进行阴道镜检查后一年内被诊断出CIN2 +,其中hrHPV阳性341例。通过McNemar检验比较了所研究的分类方法的敏感性和特异性。在预定义的临界值下,S5在hrHPV阳性女性中识别CIN2 +的敏感性高于HPV16 / 18基因分型(74%vs 54%,P = 0.04),并且特异性相似(65%vs 71%,P = 0.07)。当改变S5临界值以允许与基因分型相同的敏感性时,特异性达到91%的更高(P <0.0001)。因此,在原始筛查样本上对hrHPV阳性女性进行分诊的DNA甲基化测试可能是一种有效的方法,其性能优于基因分型。

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