Improved Diagnostic Multimodal Biomarkers for Alzheimer's Disease and Mild Cognitive Impairment

被引:9
|
作者
Martinez-Torteya, Antonio [1 ,2 ]
Trevino, Victor [1 ,2 ]
Tamez-Pena, Jose G. [1 ,2 ]
机构
[1] Catedra Bioinformat Tecnol Monterrey, Monterrey 64849, NL, Mexico
[2] Tecnol Monterrey, Escuela Med, Dept Invest & Innovac, Monterrey 64710, NL, Mexico
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
POSITRON-EMISSION-TOMOGRAPHY; NATIONAL INSTITUTE; ASSOCIATION WORKGROUPS; CEREBROSPINAL-FLUID; CORTICAL THICKNESS; CLINICAL-DIAGNOSIS; APOLIPOPROTEIN-E; DEMENTIA; RECOMMENDATIONS; PROGRESSION;
D O I
10.1155/2015/961314
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The early diagnosis of Alzheimer's disease (AD) and mild cognitive impairment (MCI) is very important for treatment research and patient care purposes. Few biomarkers are currently considered in clinical settings, and their use is still optional. The objective of this work was to determine whether multimodal and nonpreviously AD associated features could improve the classification accuracy between AD, MCI, and healthy controls, which may impact future AD biomarkers. For this, Alzheimer's Disease Neuroimaging Initiative database was mined for case-control candidates. At least 652 baseline features extracted from MRI and PET analyses, biological samples, and clinical data up to February 2014 were used. A feature selection methodology that includes a genetic algorithm search coupled to a logistic regression classifier and forward and backward selection strategies was used to explore combinations of features. This generated diagnostic models with sizes ranging from 3 to 8, including well documented AD biomarkers, as well as unexplored image, biochemical, and clinical features. Accuracies of 0.85, 0.79, and 0.80 were achieved for HC-AD, HC-MCI, and MCI-AD classifications, respectively, when evaluated using a blind test set. In conclusion, a set of features provided additional and independent information to well-established AD biomarkers, aiding in the classification of MCI and AD.
引用
收藏
页数:11
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