Wang Rui, Bing Ante, Wang Cathy, Hu Yuchen, Bosch Ronald J, DeGruttola Victor
Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School, Boston, Massachusetts, USA.
Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.
Stat Med. 2020 Jul 10;39(15):2051-2066. doi: 10.1002/sim.8529. Epub 2020 Apr 15.
Characterization of HIV viral rebound after the discontinuation of antiretroviral therapy is central to HIV cure research. We propose a parametric nonlinear mixed effects model for the viral rebound trajectory, which often has a rapid rise to a peak value followed by a decrease to a viral load set point. We choose a flexible functional form that captures the shapes of viral rebound trajectories and can also provide biological insights regarding the rebound process. Each parameter can incorporate a random effect to allow for variation in parameters across individuals. Key features of viral rebound trajectories such as viral set points are represented by the parameters in the model, which facilitates assessment of intervention effects and identification of important pretreatment interruption predictors for these features. We employ a stochastic expectation-maximization (StEM) algorithm to incorporate HIV-1 RNA values that are below the lower limit of assay quantification. We evaluate the performance of our model in simulation studies and apply the proposed model to longitudinal HIV-1 viral load data from five AIDS Clinical Trials Group treatment interruption studies.
抗逆转录病毒治疗中断后HIV病毒反弹的特征描述是HIV治愈研究的核心。我们提出了一种用于病毒反弹轨迹的参数化非线性混合效应模型,该轨迹通常会迅速上升至峰值,随后下降至病毒载量设定点。我们选择了一种灵活的函数形式,它能够捕捉病毒反弹轨迹的形状,还能提供有关反弹过程的生物学见解。每个参数都可以纳入随机效应,以考虑个体间参数的变化。病毒反弹轨迹的关键特征(如病毒设定点)由模型中的参数表示,这有助于评估干预效果,并识别这些特征的重要治疗前中断预测因素。我们采用随机期望最大化(StEM)算法来纳入低于检测定量下限的HIV-1 RNA值。我们在模拟研究中评估了模型的性能,并将所提出的模型应用于来自五项艾滋病临床试验组治疗中断研究的纵向HIV-1病毒载量数据。