Marion S A, Schechter M T
Department of Health Care and Epidemiology, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
Stat Med. 1993 Apr 15;12(7):617-31. doi: 10.1002/sim.4780120702.
Backcalculation has been used to estimate the rate of past HIV infection and to predict future AIDS incidence. In this study we examine another use: estimating the probability of progression from HIV infection to AIDS as a function of time from infection. Given observed AIDS incidence data, the technique of backcalculation estimates the most likely number of persons infected with HIV in the past. Assumptions about probability of progression from HIV infection to AIDS are necessary. By varying these assumptions and examining the resulting goodness of fit to the AIDS incidence data, we can theoretically estimate parameters of progression. We report on implementation of this method and examine its practical utility in deciding among four competing progression models specified on a priori grounds. The four specific models comprise three Weibull distributions with medians of 8, 10, and 12 years, respectively, and one model that begins as a Weibull with 8 year median but where the hazard is level after 3.5 years. To employ asymptotic maximum likelihood methods, we define a two parameter family of progression models that includes all four a priori models. One parameter sets the scale for an initial Weibull progression (the shape parameter being fixed for all models), and the other specifies a levelling point after which the hazard remains constant. AIDS incidence data from Canada's national surveillance system provided the empiric data for this evaluation. First we corrected these data for reporting delay by Poisson modelling of the delay distribution. We used three parametric families of infection curves: step-function, log-logistic, and logistic. The results support the hypothesis of an early levelling of the hazard function. When we fixed the scale parameter to that of the Weibull curve with 8 year median, the maximum likelihood estimate of the levelling point was 2.7 years, and a clearly superior fit was produced compared to a pure Weibull progression with the same scale parameter (likelihood ratio chi-square of 10.6 on 1 degree of freedom, p = 0.001). The maximum was indistinguishable in fit from the levelling point of 3.5 years hypothesized in advance (chi-square = 0.30, d.f. = 1, p = 0.58). Backcalculation, however, could not determine the Weibull scale parameter itself because the likelihood was quite flat as a function of this parameter. We conclude that one must determine the parameters governing the initial shape of the hazard function from other kinds of data.(ABSTRACT TRUNCATED AT 400 WORDS)
反向推算已被用于估计过去艾滋病毒感染率,并预测未来艾滋病发病率。在本研究中,我们探讨了它的另一种用途:估计从艾滋病毒感染进展为艾滋病的概率,该概率是感染后时间的函数。给定观察到的艾滋病发病率数据,反向推算技术可估计过去最有可能感染艾滋病毒的人数。关于从艾滋病毒感染进展为艾滋病的概率的假设是必要的。通过改变这些假设并检查由此产生的与艾滋病发病率数据的拟合优度,我们可以从理论上估计进展参数。我们报告了该方法的实施情况,并检验了其在基于先验理由指定的四个相互竞争的进展模型中进行抉择时的实际效用。这四个具体模型包括三个威布尔分布,中位数分别为8年、10年和12年,以及一个模型,该模型开始时是中位数为8年的威布尔分布,但在3.5年后风险水平保持不变。为了采用渐近最大似然法,我们定义了一个包含所有四个先验模型的双参数进展模型族。一个参数设定初始威布尔进展的尺度(形状参数对所有模型固定),另一个参数指定一个平稳点,在此之后风险保持恒定。来自加拿大国家监测系统的艾滋病发病率数据为该评估提供了经验数据。首先,我们通过对延迟分布进行泊松建模来校正这些数据的报告延迟。我们使用了三种参数化的感染曲线族:阶梯函数、对数逻辑斯蒂和逻辑斯蒂。结果支持风险函数早期平稳的假设。当我们将尺度参数固定为中位数为8年的威布尔曲线的参数时,平稳点的最大似然估计值为2.7年,与具有相同尺度参数的纯威布尔进展相比,产生了明显更好的拟合(自由度为1时似然比卡方为10.6,p = 0.001)。该最大值在拟合上与预先假设的3.5年平稳点没有区别(卡方 = 0.30,自由度 = 1,p = 0.58)。然而,反向推算无法确定威布尔尺度参数本身,因为似然作为该参数的函数相当平坦。我们得出结论,必须从其他类型的数据中确定控制风险函数初始形状的参数。(摘要截断于400字)