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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Re-detection vs. new acquisition of high-risk human papillomavirus in mid-adult women
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Re-detection vs. new acquisition of high-risk human papillomavirus in mid-adult women

机译:在中成年女性中重新发现高危人类乳头瘤病毒与新获得者

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摘要

To understand high-risk (hr) human papillomavirus (HPV) epidemiology in mid-adulthood, we assessed whether associations between incident detection of hrHPV DNA and recent sexual behavior differed according to whether or not there was serologic evidence of prior infection. From 2011 to 2012, we enrolled 409 women aged 30-50 years into a 6-month longitudinal study. We collected health and sexual behavior histories, enrollment sera for HPV antibody testing, and monthly self-collected vaginal swabs for HPV DNA genotyping. Generalized estimating equations logistic regression identified risk factors for type-specific incident hrHPV DNA, stratified by type-specific hrHPV serostatus at enrollment. Population attributable risks of hrHPV due to prior and recent exposure were estimated. When type-specific hrHPV serology was negative, recent sexual risk behavior was positively associated with incident hrHPV DNA (odds ratio in women reporting >= 3 recent sexual risk behaviors [e.g., new or multiple partners] vs. no recent sexual activity = 9.8, 95% CI: 2.4-40.6). No associations with recent sexual behavior were observed with positive type-specific hrHPV serology. Thirty percent of incident hrHPV DNA detection was attributable to prior infection (with positive serology) and 40% was attributable to recent sexual risk behavior (with negative serology). The proportion of incident hrHPV DNA detection attributable to recent sexual risk behavior decreased with increasing age. Among women with serologic evidence of prior infection, re-detection of the same hrHPV type is likely due to reactivation or intermittent detection of persistent infection. Without serologic evidence of prior infection, new detection is likely due to new acquisition or to intermittent detection of persisting infection.
机译:为了了解成人中期的高危(hr)人乳头瘤病毒(HPV)流行病学,我们根据是否有先前感染的血清学证据,评估了hrHPV DNA的事件检测与近期性行为之间的关联是否不同。从2011年到2012年,我们招募了409名30-50岁的女性参加为期6个月的纵向研究。我们收集了健康和性行为史,HPV抗体检测的入选血清,以及HPV DNA基因分型的每月一次自行收集的阴道拭子。广义估计方程逻辑回归确定了针对特定类型hrHPV DNA的危险因素,并在入学时按特定类型hrHPV血清状态进行了分层。估计了由于先前和最近的暴露而导致的hrHPV人群归因风险。当特定类型的hrHPV血清学阴性时,近期性危险行为与hrHPV DNA呈正相关(报告> = 3种近期性危险行为(例如,新伴侣或多性伴侣)的女性的患病率与无近期性行为= 9.8, 95%CI:2.4-40.6)。没有发现与阳性性特异性hrHPV血清学相关的近期性行为。 hrHPV DNA检出的百分之三十归因于先前感染(血清学呈阳性),而百分之四十归因于近期的性风险行为(血清学呈阴性)。随着年龄的增长,归因于最近的性风险行为的hrHPV DNA检测事件的比例下降。在具有先前感染的血清学证据的女性中,相同的hrHPV类型的重新检测很可能是由于持续感染的重新激活或间歇检测所致。如果没有先前感染的血清学证据,则可能由于新采集或间歇性检测持续感染而进行新检测。

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