Deep multiview learning to identify imaging-driven subtypes in mild cognitive impairment.
Deep multiview learning to identify imaging-driven subtypes in mild cognitive impairment.
复制标题
深度多视图学习识别轻度认知障碍中的成像驱动亚型。
DOI:
10.1186/s12859-022-04946-x
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发表时间:
2022-09-29
影响因子:
3
通讯作者:
Shen, Li
中科院分区:
文献类型:
--
作者:
Feng, Yixue;Kim, Mansu;Yao, Xiaohui;Liu, Kefei;Long, Qi;Shen, Li
In Alzheimer’s Diseases (AD) research, multimodal imaging analysis can unveil complementary information from multiple imaging modalities and further our understanding of the disease. One application is to discover disease subtypes using unsupervised clustering. However, existing clustering methods are often applied to input features directly, and could suffer from the curse of dimensionality with high-dimensional multimodal data. The purpose of our study is to identify multimodal imaging-driven subtypes in Mild Cognitive Impairment (MCI) participants using a multiview learning framework based on Deep Generalized Canonical Correlation Analysis (DGCCA), to learn shared latent representation with low dimensions from 3 neuroimaging modalities. DGCCA applies non-linear transformation to input views using neural networks and is able to learn correlated embeddings with low dimensions that capture more variance than its linear counterpart, generalized CCA (GCCA). We designed experiments to compare DGCCA embeddings with single modality features and GCCA embeddings by generating 2 subtypes from each feature set using unsupervised clustering. In our validation studies, we found that amyloid PET imaging has the most discriminative features compared with structural MRI and FDG PET which DGCCA learns from but not GCCA. DGCCA subtypes show differential measures in 5 cognitive assessments, 6 brain volume measures, and conversion to AD patterns. In addition, DGCCA MCI subtypes confirmed AD genetic markers with strong signals that existing late MCI group did not identify. Overall, DGCCA is able to learn effective low dimensional embeddings from multimodal data by learning non-linear projections. MCI subtypes generated from DGCCA embeddings are different from existing early and late MCI groups and show most similarity with those identified by amyloid PET features. In our validation studies, DGCCA subtypes show distinct patterns in cognitive measures, brain volumes, and are able to identify AD genetic markers. These findings indicate the promise of the imaging-driven subtypes and their power in revealing disease structures beyond early and late stage MCI. The online version contains supplementary material available at 10.1186/s12859-022-04946-x.
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DOI:
10.1016/j.jalz.2015.05.001
发表时间:
2015-07
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
Jagust WJ;Landau SM;Koeppe RA;Reiman EM;Chen K;Mathis CA;Price JC;Foster NL;Wang AY
通讯作者:
Wang AY
影响因子:
14.9
作者:
Buniello, Annalisa;MacArthur, Jacqueline A. L.;Parkinson, Helen
通讯作者:
Parkinson, Helen
影响因子:
4.6
作者:
Mitelpunkt, Alexis;Galili, Tal;Benjamini, Yoav
通讯作者:
Benjamini, Yoav
DOI:
10.1016/j.jalz.2010.03.003
发表时间:
2010-05
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
Jagust WJ;Bandy D;Chen K;Foster NL;Landau SM;Mathis CA;Price JC;Reiman EM;Skovronsky D;Koeppe RA;Alzheimer's Disease Neuroimaging Initiative
通讯作者:
Alzheimer's Disease Neuroimaging Initiative
影响因子:
4.8
作者:
Jeon, Seun;Kang, Jae Myeong;Noh, Young
通讯作者:
Noh, Young