Title | Cascaded Multi-view Canonical Correlation (CaMCCo) for Early Diagnosis of Alzheimer's Disease via Fusion of Clinical, Imaging and Omic Features. |
Publication Type | Journal Article |
Year of Publication | 2017 |
Authors | Singanamalli A, Wang H, Madabhushi A |
Corporate Authors | Alzheimer’s Disease Neuroimaging Initiative |
Journal | Sci Rep |
Volume | 7 |
Issue | 1 |
Pagination | 8137 |
Date Published | 2017 08 15 |
ISSN | 2045-2322 |
Keywords | Aged, Aged, 80 and over, Algorithms, Alzheimer Disease, Biomarkers, Case-Control Studies, Cognitive Dysfunction, Female, Genomics, Humans, Male, Models, Theoretical, Neuroimaging, Proteomics, Sensitivity and Specificity |
Abstract | The introduction of mild cognitive impairment (MCI) as a diagnostic category adds to the challenges of diagnosing Alzheimer's Disease (AD). No single marker has been proven to accurately categorize patients into their respective diagnostic groups. Thus, previous studies have attempted to develop fused predictors of AD and MCI. These studies have two main limitations. Most do not simultaneously consider all diagnostic categories and provide suboptimal fused representations using the same set of modalities for prediction of all classes. In this work, we present a combined framework, cascaded multiview canonical correlation (CaMCCo), for fusion and cascaded classification that incorporates all diagnostic categories and optimizes classification by selectively combining a subset of modalities at each level of the cascade. CaMCCo is evaluated on a data cohort comprising 149 patients for whom neurophysiological, neuroimaging, proteomic and genomic data were available. Results suggest that fusion of select modalities for each classification task outperforms (mean AUC = 0.92) fusion of all modalities (mean AUC = 0.54) and individual modalities (mean AUC = 0.90, 0.53, 0.71, 0.73, 0.62, 0.68). In addition, CaMCCo outperforms all other multi-class classification methods for MCI prediction (PPV: 0.80 vs. 0.67, 0.63). |
DOI | 10.1038/s41598-017-03925-0 |
Alternate Journal | Sci Rep |
PubMed ID | 28811553 |
PubMed Central ID | PMC5558022 |
Grant List | U01 AG024904 / AG / NIA NIH HHS / United States UL1 TR002369 / TR / NCATS NIH HHS / United States R01 CA202752 / CA / NCI NIH HHS / United States R01 CA208236 / CA / NCI NIH HHS / United States C06 RR012463 / RR / NCRR NIH HHS / United States U24 CA199374 / CA / NCI NIH HHS / United States R21 CA179327 / CA / NCI NIH HHS / United States P30 AG010129 / AG / NIA NIH HHS / United States R21 CA195152 / CA / NCI NIH HHS / United States R01 DK098503 / DK / NIDDK NIH HHS / United States |
Related Institute:
Brain Health Imaging Institute (BHII)