題名:Human Papillomavirus Genotyping for the Eight Oncogenic Types Can Improve Specificity of HPV Testing in Women with Mildly Abnormal Pap Results
作者:林景堉
Guo Ming; Lin CY; Gong Yun; Cogd David E; Zhang Wei; Lin E; Sneige Nour
貢獻者:醫學檢驗暨生物技術學系 上傳時間:2009-08-25T02:38:23Z
摘要: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 (Po0.001) in women with ASC-US, but not in women with LSIL (P¼0.52). 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; Po0.001), whereas no significant
association
was observed between the non-eight oncogenic HPV types and CIN 2/3/carcinoma (OR, 2.20; 95%CI, 0.80–6.03; P¼0.125). 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.