Luttmer Roosmarijn, Berkhof Johannes, Dijkstra Maaike G, van Kemenade Folkert J, Snijders Peter J F, Heideman Daniëlle A M, Meijer Chris J L M
VU University Medical Center, Department of Pathology, PO Box 7057, 1007 MB Amsterdam, The Netherlands.
VU University Medical Center, Department of Epidemiology & Biostatistics, PO Box 7057, 1007 MB Amsterdam, The Netherlands.
J Clin Virol. 2015 Jun;67:59-66. doi: 10.1016/j.jcv.2015.04.004. Epub 2015 Apr 7.
High-risk human papillomavirus (hrHPV) DNA positive women require triage testing to identify those with high-grade cervical intraepithelial neoplasia or cancer (≥CIN2).
Comparing three triage algorithms (1) E7 mRNA testing following HPV16/18/31/33/45/52/58 genotyping (E7 mRNA test), (2) HPV16/18 DNA genotyping and (3) cytology, for ≥CIN2 detection in hrHPV DNA-positive women.
hrHPV DNA-positive women aged 18-63 years visiting gynecology outpatient clinics were included in a prospective observational cohort study. From these women a cervical scrape and colposcopy-directed biopsies were obtained. Cervical scrapes were evaluated by cytology, HPV DNA genotyping by bead-based multiplex genotyping of GP5+6+-PCR-products, and presence of HPV16/18/31/33/45/52/58 E7 mRNA using nucleic acid sequence-based amplification (NASBA) in DNA positive women for respective HPV types. Sensitivities and specificities for ≥CIN2 were compared between E7 mRNA test and HPV16/18 DNA genotyping in the total group (n=348), and E7 mRNA test and cytology in a subgroup of women referred for non-cervix-related gynecological complaints (n=133).
Sensitivity for ≥CIN2 of the E7 mRNA test was slightly higher than that of HPV16/18 DNA genotyping (66.9% versus 60.9%; ratio 1.10, 95% CI: 1.0002-1.21), at similar specificity (54.8% versus 52.3%; ratio 1.05, 95% CI: 0.93-1.18). Neither sensitivity nor specificity of the E7 mRNA test differed significantly from that of cytology (sensitivity: 68.8% versus 75.0%; ratio 0.92, 95% CI: 0.72-1.17; specificity: 59.4% versus 65.3%; ratio 0.91, 95% CI: 0.75-1.10).
For detection of ≥CIN2 in hrHPV DNA-positive women, an algorithm including E7 mRNA testing following HPV16/18/31/33/45/52/58 DNA genotyping performs similar to HPV16/18 DNA genotyping or cytology.
高危型人乳头瘤病毒(hrHPV)DNA检测呈阳性的女性需要进行分流检测,以确定那些患有高级别宫颈上皮内瘤变或癌症(≥CIN2)的患者。
比较三种分流检测算法:(1)HPV16/18/31/33/45/52/58基因分型后进行E7 mRNA检测(E7 mRNA检测);(2)HPV16/18 DNA基因分型;(3)细胞学检查,用于检测hrHPV DNA阳性女性中的≥CIN2。
年龄在18 - 63岁的hrHPV DNA阳性且前往妇科门诊就诊的女性被纳入一项前瞻性观察队列研究。从这些女性中获取宫颈刮片和阴道镜引导下的活检组织。宫颈刮片通过细胞学检查进行评估,HPV DNA基因分型采用基于磁珠的GP5 + 6 + -PCR产物多重基因分型法,对于DNA阳性的女性,使用基于核酸序列扩增(NASBA)的方法检测HPV16/18/31/33/45/52/58 E7 mRNA。在总人群(n = 348)中比较E7 mRNA检测和HPV16/18 DNA基因分型对≥CIN2的敏感性和特异性,在因非宫颈相关妇科疾病转诊的女性亚组(n = 133)中比较E7 mRNA检测和细胞学检查对≥CIN2的敏感性和特异性。
E7 mRNA检测对≥CIN2的敏感性略高于HPV16/18 DNA基因分型(66.9%对60.9%;比值1.10,95%CI:1.0002 - 1.21),特异性相似(54.8%对52.3%;比值1.05,95%CI:0.93 - 1.18)。E7 mRNA检测的敏感性和特异性与细胞学检查相比均无显著差异(敏感性:68.8%对75.0%;比值0.92,95%CI:0.72 - 1.17;特异性:59.4%对65.3%;比值0.91,95%CI:0.75 - 1.10)。
对于检测hrHPV DNA阳性女性中的≥CIN2,一种包括HPV16/18/31/33/45/52/58 DNA基因分型后进行E7 mRNA检测的算法与HPV16/18 DNA基因分型或细胞学检查的效果相似。