Hwang Loris Y, Ma Yifei, Shiboski Stephen C, Farhat Sepideh, Jonte Janet, Moscicki Anna-Barbara
University of California San Francisco, Department of Pediatrics, Division of Adolescent Medicine, 3333 California Street, Suite 245, San Francisco, CA 94118, USA.
J Infect Dis. 2012 Aug 15;206(4):504-11. doi: 10.1093/infdis/jis398. Epub 2012 Jun 13.
Vulnerability of younger women to human papillomavirus 16 (HPV16) infection has been attributed to the predominance of ectocervical columnar epithelia in this age group. However, squamous metaplastic tissue may be more influential. We examined the extent of ectopy and metaplastic activity as risks for HPV16 acquisition in a prospective cohort.
Participants were HPV16 negative at the first two visits. Follow-up occurred every 4 months. Ectopy was quantitatively measured on colpophotographs. We calculated metaplastic rate as the difference in ectopy between visits. Cox proportional hazards models were constructed, adjusting for several covariates.
Analyses included 198 women (mean baseline age 17 years) for 1734 visits. Mean follow-up was 4.4 years. Incident HPV16 was detected in 36 (18%) women. Metaplastic rate between the two visits before HPV16 detection was significantly associated with incident infection (hazard ratio [HR], 1.17; confidence interval [CI], 1.02-1.33; P = .02). However, ectopy was not significant, whether measured before or concurrent to HPV16 detection (HR range, 0.99-1.00; CI range, .97-1.02; P range, .47-.65).
Dynamic metaplasia rather than the sheer extent of ectopy appears to increase risk for incident HPV16 in healthy young women. This in vivo observation is consistent with the HPV life cycle, during which host cell replication and differentiation supports viral replication.
年轻女性对人乳头瘤病毒16型(HPV16)感染的易感性归因于该年龄组中外宫颈柱状上皮占优势。然而,鳞状化生组织可能更具影响力。我们在一个前瞻性队列中研究了异位和化生活动程度作为HPV16感染风险的情况。
参与者在前两次就诊时HPV16呈阴性。每4个月进行一次随访。通过阴道镜照片对异位进行定量测量。我们将化生率计算为两次就诊之间异位的差异。构建Cox比例风险模型,并对多个协变量进行调整。
分析纳入了198名女性(平均基线年龄17岁),共进行了1734次就诊。平均随访时间为4.4年。在36名(18%)女性中检测到HPV16感染。在HPV16检测前两次就诊之间的化生率与感染发生率显著相关(风险比[HR],1.17;置信区间[CI],1.02 - 1.33;P = 0.02)。然而,异位不显著,无论在HPV16检测之前还是同时测量(HR范围,0.99 - 1.00;CI范围,0.97 - 1.02;P范围,0.47 - 0.65)。
动态化生而非单纯的异位程度似乎会增加健康年轻女性感染HPV16的风险。这一体内观察结果与HPV生命周期一致,在此期间宿主细胞的复制和分化支持病毒复制。