Comparison of GP5+/6+-PCR and SPF10-line blot assays for detection of high-risk human papillomavirus in samples from women with normal cytology results who develop grade 3 cervical intraepithelial neoplasia

被引:42
作者
Hesselink, A. T. [1 ]
van Ham, M. A. P. C. [2 ]
Heideman, D. A. M. [1 ]
Groothuismink, Z. M. A. [1 ]
Rozendaal, L. [1 ]
Berkhof, J. [3 ]
van Kemenade, F. J. [1 ]
Massuger, L. A. F. G. [2 ]
Melchers, W. J. G. [4 ]
Meijer, C. J. L. M. [1 ]
Snijders, P. J. F. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Pathol, NL-1081 HV Amsterdam, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Obstet & Gynecol, NL-6525 ED Nijmegen, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Biostat & Epidemiol, NL-1081 HV Amsterdam, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, NL-6525 ED Nijmegen, Netherlands
关键词
D O I
10.1128/JCM.00476-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Using a case control approach, we performed a two-way comparison study between GP5+/6+-PCR and HPV SPF10-Line Blot 25 (SPF10) assays for detection of 14 types of high-risk human papillomavirus (hrHPV) in samples from women with normal cytology results who had or developed grade 3 cervical intraepithelial neoplasia (CIN 3). Samples were pooled from two cohorts, i.e., women participating in population-based screening and women attending a gynecological outpatient clinic. Cases (n = 45) were women with histologically confirmed CIN 3 diagnosed within a median follow-up time of 2.7 (range, 0.2 to 7.9) years. Control samples were from women (n = 264) who had developed CIN 1 lesions at maximum (median follow-up at 5.8 [ range, 0 to 10] years). Identical numbers of cases tested positive for 1 or more of the 14 hrHPV types by both systems (40/45; McNemar; P = 1.0). Conversely, SPF10 scored significantly more controls as hrHPV positive than did GP5+/6+-PCR (95/264 versus 29/264; McNemar; P < 0.001). Consequently, women with normal cytology results and an hrHPV GP5+/6+-PCR-positive test exhibited a risk of CIN 3 that was 4.5 times higher (odds ratio [OR], 65; 95% confidence interval [95% CI], 24 to 178) than that seen for women with an hrHPV-positive SPF10 test (OR, 14; 95% CI, 5 to 38)). Similar results were obtained after analysis of both cohorts separately. Discrepancy analysis by viral load assessment for the most common discordant hrHPV types (HPV16, -18, and -52) showed that samples which were SPF10 positive only for these types had viral loads significantly lower than those for samples that were positive by both assays (analysis of variance; P < 0.006). Our data indicate that GP5+/6+-PCR has a better clinical performance than SPF10 for women who are diagnosed with CIN 3 after prior normal cytology results. The extra positivity scored by SPF10 mainly involved infections characterized by low viral loads that do not result in CIN 3.
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收藏
页码:3215 / 3221
页数:7
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