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Human papillomavirus genotyping for the eight oncogenic types can improve specificity of HPV testing in women with mildly abnormal Pap results

机译:八种致癌类型的人乳头瘤病毒基因分型可以提高轻度巴氏结果异常的女性中HPV检测的特异性

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To evaluate whether human papillomavirus (HPV) genotyping for the selected oncogenic HPV types can improve the efficacy of HPV DNA testing in predicting cervical intraepithelial neoplasia (CIN 2/3) in women with mildly abnormal Pap results, we compared HPV DNA testing and HPV genotyping for eight oncogenic types (16, 18, 31, 33, 35, 45, 52 and 58) in Pap specimens with abnormal results (HSIL, 20 cases; LSIL, 42 cases; ASC-US, 94 cases) and follow-up biopsies. Using consensus primer-mediated PCR assays, HPV DNA was detected in 90% (18/20) of HSIL, 95% (40/42) of LSIL and 64% (60/94) of ASC-US cases. HPV DNA positivity was significantly associated with CIN 2/3/carcinoma (PP=0.52). Of HPV DNA-positive specimens, the eight oncogenic HPV types were detected in 83% of HSIL cases (15/18), 53% of LSIL cases (21/40), and 47% of ASC-US cases (28/60). The eight oncogenic HPV types were significantly associated with CIN 2/3/carcinoma (OR, 10.6; 95% CI, 3.98–28.10; PP=0.125). In women with ASC-US, HPV genotyping for the eight oncogenic types showed higher specificity (81 vs 46%) and positive predictive value (PPV, 44 vs 26%) in predicting CIN 2/3/carcinoma compared to HPV DNA testing. Similarly, in women with LSIL, higher specificity (69 vs 8%) and PPV (62 vs 39%) for predicting CIN 2/3/carcinoma were also observed using HPV genotyping test for the eight oncogenic types compared to HPV DNA testing. Our findings suggested that HPV genotyping for the eight oncogenic types might be useful to improve the efficacy of HPV DNA testing for predicting CIN 2/3/carcinoma in women with mildly abnormal Pap results, which may lead to personalized clinical management with improved patient compliance for follow-up.
机译:为了评估选择的致癌HPV类型的人乳头瘤病毒(HPV)基因分型是否可以提高HPV DNA检测在预测轻度异常巴氏结果的女性宫颈上皮内瘤变(CIN 2/3)中的功效,我们比较了HPV DNA检测和HPV基因分型在巴氏标本中检测到八种致癌类型(16、18、31、33、35、45、52和58),结果异常(HSIL,20例; LSIL,42例; ASC-US,94例)和随访活检。使用共有引物介导的PCR分析,在90%(18/20)的HSIL,95%(40/42)的LSIL和64%(60/94)的ASC-US病例中检测到HPV DNA。 HPV DNA阳性与CIN 2/3 /癌显着相关(PP = 0.52)。在HPV DNA阳性标本中,在83%的HSIL病例(15/18),53%的LSIL病例(21/40)和47%的ASC-US病例(28)中检测到8种致癌HPV类型/ 60)。八种致癌HPV类型与CIN 2/3 /癌显着相关(OR为10.6; 95%CI为3.98-28.10; PP = 0.125)。在患有ASC-US的女性中,与HPV DNA检测相比,八种致癌类型的HPV基因分型在预测CIN 2/3 /癌中显示出更高的特异性(81 vs 46 %)和阳性预测值(PPV,44 vs 26 %)。 。同样,在LSIL女性中,与HPV DNA测试相比,使用HPV基因分型测试对八种致癌类型的预测CIN 2/3 /癌的特异性更高(69 vs 8 %)和PPV(62 vs 39 %)。 。我们的研究结果表明,针对八种致癌类型的HPV基因分型可能有助于提高HPV DNA检测预测Pap结果轻度异常的女性的CIN 2/3 /癌的功效,这可能导致个性化的临床管理并改善患者的依从性跟进。

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