Uncovering the heterogeneity in the disease progression of Alzheimer's is a key factor to disease understanding and treatment development, so that interventions can be tailored to target the subgroups that will benefit most from the treatment, which is an important goal of precision medicine. However, in practice, one top methodological challenge hindering the heterogeneity investigation is that the true subgroup membership of each individual is often unknown. In this article, we aim to identify latent subgroups of individuals who share a common disorder progress over time, to predict latent subgroup memberships, and to estimate and infer the heterogeneous trajectories among the subgroups. To achieve these goals, we apply a concave fusion learning method proposed in Ma and Huang (2017) and Ma et al. (2019) to conduct subgroup analysis for longitudinal trajectories of the Alzheimer's disease data. The heterogeneous trajectories are represented by subject-specific unknown functions which are approximated by B-splines. The concave fusion method can simultaneously estimate the spline coefficients and merge them together for the subjects belonging to the same subgroup to automatically identify subgroups and recover the heterogeneous trajectories. The resulting estimator of the disease trajectory of each subgroup is supported by an asymptotic distribution. It provides a sound theoretical basis for further conducting statistical inference in subgroup analysis..
翻译:阿尔茨海默氏病发病的异质性变异,是了解和治疗疾病发展的一个关键因素,因此,干预措施可以针对最能从治疗中受益的分组进行调整,这是精确医学的一个重要目标。然而,在实践中,阻碍异质性调查的最主要方法挑战是,每个人的真正分组成员身份往往不为人所知。在本篇文章中,我们的目标是确定长期具有共同障碍进展的个人的潜在分组,预测潜在分组成员,估计和推断各分组的不同轨迹。为实现这些目标,我们在马和黄(2017年)和马等人(2019年)中建议采用同源聚合学习方法,对阿尔茨海默氏病数据的纵向轨迹进行分组分析。混杂轨迹由B-spline所近似的具体主题未知功能所代表。同源聚合方法可以同时估计样点系数,并结合属于同一分组的主体。为了实现这些目标,我们采用了在马和黄(2017年)和马等人(2019年)中建议的一种同源聚合学习方法,对马和黄(2017年)和黄等人(2019年)进行分组进行分组分析,以进行分组分组分析,以便对阿尔茨海氏病状分布分析进行分组进行分组分析,以进一步恢复其结果分组分析的分类分析。这种分析,这种分析,它支持的分类分析,进一步提供结果的分类分析。