Aregay Mehreteab, Shkedy Ziv, Molenberghs Geert, David Marie-Pierre, Tibaldi Fabián
a I-BioStat, Katholieke Universiteit Leuven , Leuven , Belgium.
J Biopharm Stat. 2013;23(6):1228-48. doi: 10.1080/10543406.2013.834917.
In infectious diseases, it is important to predict the long-term persistence of vaccine-induced antibodies and to estimate the time points where the individual titers are below the threshold value for protection. This article focuses on HPV-16/18, and uses a so-called fractional-polynomial model to this effect, derived in a data-driven fashion. Initially, model selection was done from among the second- and first-order fractional polynomials on the one hand and from the linear mixed model on the other. According to a functional selection procedure, the first-order fractional polynomial was selected. Apart from the fractional polynomial model, we also fitted a power-law model, which is a special case of the fractional polynomial model. Both models were compared using Akaike's information criterion. Over the observation period, the fractional polynomials fitted the data better than the power-law model; this, of course, does not imply that it fits best over the long run, and hence, caution ought to be used when prediction is of interest. Therefore, we point out that the persistence of the anti-HPV responses induced by these vaccines can only be ascertained empirically by long-term follow-up analysis.
在传染病领域,预测疫苗诱导抗体的长期持久性并估计个体滴度低于保护阈值的时间点非常重要。本文聚焦于HPV - 16/18,并为此使用了一种以数据驱动方式推导的所谓分数多项式模型。最初,模型选择一方面在二阶和一阶分数多项式之间进行,另一方面在线性混合模型之间进行。根据功能选择程序,选择了一阶分数多项式。除了分数多项式模型,我们还拟合了一个幂律模型,它是分数多项式模型的一个特殊情况。使用赤池信息准则对这两个模型进行了比较。在观察期内,分数多项式比幂律模型更能拟合数据;当然,这并不意味着从长远来看它拟合得最好,因此,当涉及预测时应谨慎使用。所以,我们指出这些疫苗诱导的抗HPV反应的持久性只能通过长期随访分析凭经验确定。