Bayesian hidden Markov models for delineating the pathology of Alzheimer's disease

被引:22
作者
Kang, Kai [1 ]
Cai, Jingheng [2 ]
Song, Xinyuan [1 ,3 ]
Zhu, Hongtu [4 ]
机构
[1] Chinese Univ Hong Kong, Dept Stat, Hong Kong, Peoples R China
[2] Sun Yat Sen Univ, Dept Stat, Guangzhou, Guangdong, Peoples R China
[3] Chinese Univ Hong Kong, Shenzhen Res Inst, Hong Kong, Peoples R China
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
基金
中国国家自然科学基金;
关键词
Bayesian P-splines; correlated random effects; hidden Markov models; MCMC methods; semiparametric models; MILD COGNITIVE IMPAIRMENT; LATENT VARIABLE MODELS; LONGITUDINAL DATA; HIPPOCAMPAL; EXTENSION; DIAGNOSIS; SURVIVAL; SPLINES; TIME;
D O I
10.1177/0962280217748675
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Alzheimer's disease is a firmly incurable and progressive disease. The pathology of Alzheimer's disease usually evolves from cognitive normal, to mild cognitive impairment, to Alzheimer's disease. The aim of this paper is to develop a Bayesian hidden Markov model to characterize disease pathology, identify hidden states corresponding to the diagnosed stages of cognitive decline, and examine the dynamic changes of potential risk factors associated with the cognitive normal-mild cognitive impairment-Alzheimer's disease transition. The hidden Markov model framework consists of two major components. The first one is a state-dependent semiparametric regression for delineating the complex associations between clinical outcomes of interest and a set of prognostic biomarkers across neurodegenerative states. The second one is a parametric transition model, while accounting for potential covariate effects on the cross-state transition. The inter-individual and inter-process differences are taken into account via correlated random effects in both components. Based on the Alzheimer's Disease Neuroimaging Initiative data set, we are able to identify four states of Alzheimer's disease pathology, corresponding to common diagnosed cognitive decline stages, including cognitive normal, early mild cognitive impairment, late mild cognitive impairment, and Alzheimer's disease and examine the effects of hippocampus, age, gender, and APOE-epsilon 4 on degeneration of cognitive function across the four cognitive states.
引用
收藏
页码:2112 / 2124
页数:13
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