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Predicting Clinical Scores From Magnetic Resonance Scans in Alzheimer Disease - 2010

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Predicting Clinical Scores From Magnetic Resonance Scans in Alzheimer Disease | S-Logix

Research Area:  Machine Learning

Abstract:

Machine learning and pattern recognition methods have been used to diagnose Alzheimers disease (AD) and mild cognitive impairment (MCI) from individual MRI scans. Another application of such methods is to predict clinical scores from individual scans. Using relevance vector regression (RVR), we predicted individuals performances on established tests from their MRI T1 weighted image in two independent data sets. From Mayo Clinic, 73 probable AD patients and 91 cognitively normal (CN) controls completed the Mini-Mental State Examination (MMSE), Dementia Rating Scale (DRS), and Auditory Verbal Learning Test (AVLT) within 3 months of their scan. Baseline MRI from the Alzheimer disease Neuroimaging Initiative (ADNI) comprised the other data set; 113 AD, 351 MCI, and 122 CN subjects completed the MMSE and Alzheimer Disease Assessment Scale—Cognitive subtest (ADAS-cog) and 39 AD, 92 MCI, and 32 CN ADNI subjects completed MMSE, ADAS-cog, and AVLT. Predicted and actual clinical scores were highly correlated for the MMSE, DRS, and ADAS-cog tests (P < 0.0001). Training with one data set and testing with another demonstrated stability between data sets. DRS, MMSE, and ADAS-Cog correlated better than AVLT with whole brain grey matter changes associated with AD. This result underscores their utility for screening and tracking disease. RVR offers a novel way to measure interactions between structural changes and neuropsychological tests beyond that of univariate methods. In clinical practice, we envision using RVR to aid in diagnosis and predict clinical outcome.

Keywords:  
Alzheimer disease
Multivariate
Machine learning
Relevance vector regression
MMSE
DRS
AVLT
ADAS-Cog

Author(s) Name:  Stonnington, Cynthia M., Carlton Chu, Stefan Klöppel

Journal name:  NeuroImage

Conferrence name:  

Publisher name:  Elsevier

DOI:  10.1016/j.neuroimage.2010.03.051

Volume Information:  Volume 51