TY - JOUR
T1 - Machine learning on longitudinal multi-modal data enables the understanding and prognosis of Alzheimer's disease progression
AU - for the Alzheimer's Disease Neuroimaging Initiative and the Australian Imaging Biomarkers and Lifestyle Study of Aging
AU - Zhang, Suixia
AU - Yuan, Jing
AU - Sun, Yu
AU - Wu, Fei
AU - Liu, Ziyue
AU - Zhai, Feifei
AU - Zhang, Yaoyun
AU - Somekh, Judith
AU - Peleg, Mor
AU - Zhu, Yi Cheng
AU - Huang, Zhengxing
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/7/19
Y1 - 2024/7/19
N2 - Alzheimer's disease (AD) is a complex pathophysiological disease. Allowing for heterogeneity, not only in disease manifestations but also in different progression patterns, is critical for developing effective disease models that can be used in clinical and research settings. We introduce a machine learning model for identifying underlying patterns in Alzheimer's disease (AD) trajectory using longitudinal multi-modal data from the ADNI cohort and the AIBL cohort. Ten biologically and clinically meaningful disease-related states were identified from data, which constitute three non-overlapping stages (i.e., neocortical atrophy [NCA], medial temporal atrophy [MTA], and whole brain atrophy [WBA]) and two distinct disease progression patterns (i.e., NCA → WBA and MTA → WBA). The index of disease-related states provided a remarkable performance in predicting the time to conversion to AD dementia (C-Index: 0.923 ± 0.007). Our model shows potential for promoting the understanding of heterogeneous disease progression and early predicting the conversion time to AD dementia.
AB - Alzheimer's disease (AD) is a complex pathophysiological disease. Allowing for heterogeneity, not only in disease manifestations but also in different progression patterns, is critical for developing effective disease models that can be used in clinical and research settings. We introduce a machine learning model for identifying underlying patterns in Alzheimer's disease (AD) trajectory using longitudinal multi-modal data from the ADNI cohort and the AIBL cohort. Ten biologically and clinically meaningful disease-related states were identified from data, which constitute three non-overlapping stages (i.e., neocortical atrophy [NCA], medial temporal atrophy [MTA], and whole brain atrophy [WBA]) and two distinct disease progression patterns (i.e., NCA → WBA and MTA → WBA). The index of disease-related states provided a remarkable performance in predicting the time to conversion to AD dementia (C-Index: 0.923 ± 0.007). Our model shows potential for promoting the understanding of heterogeneous disease progression and early predicting the conversion time to AD dementia.
KW - machine learning
KW - neuroscience
UR - http://www.scopus.com/inward/record.url?scp=85196856335&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2024.110263
DO - 10.1016/j.isci.2024.110263
M3 - Article
AN - SCOPUS:85196856335
SN - 2589-0042
VL - 27
JO - iScience
JF - iScience
IS - 7
M1 - 110263
ER -