Identifying progression subphenotypes of Alzheimer's disease from large-scale electronic health records with machine learning.

TitleIdentifying progression subphenotypes of Alzheimer's disease from large-scale electronic health records with machine learning.
Publication TypeJournal Article
Year of Publication2025
AuthorsZhou M, Tang AS, Zhang H, Xu Z, Ke AMC, Su C, Huang Y, Mantyh WG, Jaffee MS, Rankin KP, DeKosky ST, Zhou J, Guo Y, Bian J, Sirota M, Wang F
JournalJ Biomed Inform
Volume165
Pagination104820
Date Published2025 May
ISSN1532-0480
KeywordsAged, Aged, 80 and over, Alzheimer Disease, Cognitive Dysfunction, Databases, Factual, Disease Progression, Electronic Health Records, Female, Humans, Machine Learning, Male, Phenotype, United States
Abstract

OBJECTIVE: Identification of clinically meaningful subphenotypes of disease progression can enhance the understanding of disease heterogeneity and underlying pathophysiology. In this study, we propose a machine learning framework to identify subphenotypes of Alzheimer's disease progression based on longitudinal real-world patient records.

METHODS: The framework, dynaPhenoM, extracts coherent clinical topics across patient visits and employs a time-aware latent class analysis to characterize subphenotypes. We validated dynaPhenoM using three patient databases with a total of 3952 AD patients across the United States, demonstrating its effectiveness in revealing mild cognitive impairment (MCI) progression to AD.

RESULTS: Our study identified five subphenotypes associated with distinct organ systems for disease progression from MCI to AD, including common subtypes across cohorts-respiratory, musculoskeletal, cardiovascular, and endocrine/metabolic-as well as a cohort-specific digestive subtype.

CONCLUSION: Our study unravels the complexity and heterogeneity of the progression from MCI to AD. These findings highlight disease progression heterogeneity and can inform both diagnostic and therapeutic strategies, thereby advancing precision medicine for Alzheimer's disease.

DOI10.1016/j.jbi.2025.104820
Alternate JournalJ Biomed Inform
PubMed ID40180206
PubMed Central IDPMC12296293
Grant ListRF1 AG084178 / AG / NIA NIH HHS / United States
T32 GM007618 / GM / NIGMS NIH HHS / United States
R01 AG060393 / AG / NIA NIH HHS / United States
R01 AG080624 / AG / NIA NIH HHS / United States
R01 AG072449 / AG / NIA NIH HHS / United States
R01 NS140142 / NS / NINDS NIH HHS / United States
R01 AG076234 / AG / NIA NIH HHS / United States
RF1 AG072449 / AG / NIA NIH HHS / United States
R01 AG080806 / AG / NIA NIH HHS / United States
F30 AG079504 / AG / NIA NIH HHS / United States
R01 AG076448 / AG / NIA NIH HHS / United States
R01 AG080991 / AG / NIA NIH HHS / United States
Division: 
Institute of Artificial Intelligence for Digital Health
Category: 
Faculty Publication