Predicting Progression from Mild Cognitive Impairment to Alzheimer's Dementia Using Clinical, MRI, and Plasma Biomarkers via Probabilistic Pattern Classification

Individuals with mild cognitive impairment (MCI) have a substantially increased risk of developing dementia due to Alzheimer's disease (AD). In this study, we developed a multivariate prognostic model for predicting MCI-to-dementia progression at the individual patient level. Using baseline dat...

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Veröffentlicht in:PloS one 2016-02, Vol.11 (2), p.e0138866-e0138866
Hauptverfasser: Korolev, Igor O, Symonds, Laura L, Bozoki, Andrea C
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description Individuals with mild cognitive impairment (MCI) have a substantially increased risk of developing dementia due to Alzheimer's disease (AD). In this study, we developed a multivariate prognostic model for predicting MCI-to-dementia progression at the individual patient level. Using baseline data from 259 MCI patients and a probabilistic, kernel-based pattern classification approach, we trained a classifier to distinguish between patients who progressed to AD-type dementia (n = 139) and those who did not (n = 120) during a three-year follow-up period. More than 750 variables across four data sources were considered as potential predictors of progression. These data sources included risk factors, cognitive and functional assessments, structural magnetic resonance imaging (MRI) data, and plasma proteomic data. Predictive utility was assessed using a rigorous cross-validation framework. Cognitive and functional markers were most predictive of progression, while plasma proteomic markers had limited predictive utility. The best performing model incorporated a combination of cognitive/functional markers and morphometric MRI measures and predicted progression with 80% accuracy (83% sensitivity, 76% specificity, AUC = 0.87). Predictors of progression included scores on the Alzheimer's Disease Assessment Scale, Rey Auditory Verbal Learning Test, and Functional Activities Questionnaire, as well as volume/cortical thickness of three brain regions (left hippocampus, middle temporal gyrus, and inferior parietal cortex). Calibration analysis revealed that the model is capable of generating probabilistic predictions that reliably reflect the actual risk of progression. Finally, we found that the predictive accuracy of the model varied with patient demographic, genetic, and clinical characteristics and could be further improved by taking into account the confidence of the predictions. We developed an accurate prognostic model for predicting MCI-to-dementia progression over a three-year period. The model utilizes widely available, cost-effective, non-invasive markers and can be used to improve patient selection in clinical trials and identify high-risk MCI patients for early treatment.
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In this study, we developed a multivariate prognostic model for predicting MCI-to-dementia progression at the individual patient level. Using baseline data from 259 MCI patients and a probabilistic, kernel-based pattern classification approach, we trained a classifier to distinguish between patients who progressed to AD-type dementia (n = 139) and those who did not (n = 120) during a three-year follow-up period. More than 750 variables across four data sources were considered as potential predictors of progression. These data sources included risk factors, cognitive and functional assessments, structural magnetic resonance imaging (MRI) data, and plasma proteomic data. Predictive utility was assessed using a rigorous cross-validation framework. Cognitive and functional markers were most predictive of progression, while plasma proteomic markers had limited predictive utility. The best performing model incorporated a combination of cognitive/functional markers and morphometric MRI measures and predicted progression with 80% accuracy (83% sensitivity, 76% specificity, AUC = 0.87). Predictors of progression included scores on the Alzheimer's Disease Assessment Scale, Rey Auditory Verbal Learning Test, and Functional Activities Questionnaire, as well as volume/cortical thickness of three brain regions (left hippocampus, middle temporal gyrus, and inferior parietal cortex). Calibration analysis revealed that the model is capable of generating probabilistic predictions that reliably reflect the actual risk of progression. Finally, we found that the predictive accuracy of the model varied with patient demographic, genetic, and clinical characteristics and could be further improved by taking into account the confidence of the predictions. We developed an accurate prognostic model for predicting MCI-to-dementia progression over a three-year period. The model utilizes widely available, cost-effective, non-invasive markers and can be used to improve patient selection in clinical trials and identify high-risk MCI patients for early treatment.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26901338</pmid><doi>10.1371/journal.pone.0138866</doi><oa>free_for_read</oa></addata></record>
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subjects Aged
Aged, 80 and over
Aging
Alzheimer Disease - blood
Alzheimer Disease - physiopathology
Alzheimer's disease
Alzheimers disease
Auditory discrimination learning
Biology and Life Sciences
Biomarkers
Biomarkers - blood
Brain
Classification
Clinical trials
Cognitive ability
Cognitive Dysfunction - blood
Cognitive Dysfunction - physiopathology
Cortex (auditory)
Cortex (parietal)
Cortex (temporal)
Data sources
Dementia
Dementia - blood
Dementia - physiopathology
Dementia disorders
Demographics
Disease Progression
Female
Functional magnetic resonance imaging
Humans
Impairment
Magnetic resonance
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Male
Mathematical models
Medical imaging
Medical research
Medicine and Health Sciences
Models, Theoretical
Neurodegenerative diseases
Neuroimaging
Neurology
Neurosciences
NMR
Nuclear magnetic resonance
Patients
Pattern classification
Performance prediction
Physical Sciences
Plasmas (physics)
Research and Analysis Methods
Risk analysis
Risk assessment
Risk factors
Structure-function relationships
Studies
Temporal gyrus
Temporal lobe
title Predicting Progression from Mild Cognitive Impairment to Alzheimer's Dementia Using Clinical, MRI, and Plasma Biomarkers via Probabilistic Pattern Classification
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