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首页> 外文期刊>American Journal of Epidemiology >Bias Due to Correlation Between Times-at-Risk for Infection in Epidemiologic Studies Measuring Biological Interactions Between Sexually Transmitted Infections: A Case Study Using Human Papillomavirus Type Interactions
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Bias Due to Correlation Between Times-at-Risk for Infection in Epidemiologic Studies Measuring Biological Interactions Between Sexually Transmitted Infections: A Case Study Using Human Papillomavirus Type Interactions

机译:在流行病学研究中,风险传播时间之间的相关性导致的偏差,用于测量性传播感染之间的生物学相互作用:使用人乳头瘤病毒类型相互作用的案例研究

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摘要

The clustering of human papillomavirus (HPV) infections in some individuals is often interpreted as the result of common risk factors rather than biological interactions between different types of HPV. The intraindividual correlation between times-at-risk for all HPV infections is not generally considered in the analysis of epidemiologic studies. We used a deterministic transmission model to simulate cross-sectional and prospective epidemiologic studies measuring associations between 2 HPV types. When we assumed no interactions, the model predicted that studies would estimate odds ratios and incidence rate ratios greater than 1 between HPV types even after complete adjustment for sexual behavior. We demonstrated that this residual association is due to correlation between the times-at-risk for different HPV types, where individuals become concurrently at risk for all of their partners' HPV types when they enter a partnership and are not at risk when they are single. This correlation can be controlled in prospective studies by restricting analyses to susceptible individuals with an infected sexual partner. The bias in the measured associations was largest in low-sexual-activity populations, cross-sectional studies, and studies which evaluated infection with a first HPV type as the exposure. These results suggest that current epidemiologic evidence does not preclude the existence of competitive biological interactions between HPV types.
机译:人乳头瘤病毒(HPV)感染在某些个体中的聚集通常被解释为常见危险因素的结果,而不是不同类型HPV之间的生物学相互作用的结果。在流行病学研究分析中,通常不会考虑所有HPV感染的风险时间之间的个体差异。我们使用确定性传播模型来模拟横断面和前瞻性流行病学研究,以测量2种HPV类型之间的关联。当我们假设没有相互作用时,该模型预测即使完全调整了性行为,HPV类型之间的比值比和发生率比也将大于1。我们证明了这种残留关联是由于不同HPV类型的风险时间之间的相关性所致,在这种情况下,个人在进入合伙关系时同时面临所有合伙人所有HPV类型的风险,而在单身时则没有风险。通过将分析限制在具有感染性伴侣的易感个体中,可以在前瞻性研究中控制这种相关性。在低性活动人群,横断面研究和评估以第一种HPV类型作为感染的感染的研究中,所测得的联想的偏差最大。这些结果表明,当前的流行病学证据并不排除HPV类型之间存在竞争性生物学相互作用。

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