Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.

Computational models predicting symptomatic progression at the individual level can be highly beneficial for early intervention and treatment planning for Alzheimer's disease (AD). Individual prognosis is complicated by many factors including the definition of the prediction objective itself. I...

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Main Authors: Nikhil Bhagwat, Joseph D Viviano, Aristotle N Voineskos, M Mallar Chakravarty, Alzheimer’s Disease Neuroimaging Initiative
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-09-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC6157905?pdf=render
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author Nikhil Bhagwat
Joseph D Viviano
Aristotle N Voineskos
M Mallar Chakravarty
Alzheimer’s Disease Neuroimaging Initiative
author_facet Nikhil Bhagwat
Joseph D Viviano
Aristotle N Voineskos
M Mallar Chakravarty
Alzheimer’s Disease Neuroimaging Initiative
author_sort Nikhil Bhagwat
collection DOAJ
description Computational models predicting symptomatic progression at the individual level can be highly beneficial for early intervention and treatment planning for Alzheimer's disease (AD). Individual prognosis is complicated by many factors including the definition of the prediction objective itself. In this work, we present a computational framework comprising machine-learning techniques for 1) modeling symptom trajectories and 2) prediction of symptom trajectories using multimodal and longitudinal data. We perform primary analyses on three cohorts from Alzheimer's Disease Neuroimaging Initiative (ADNI), and a replication analysis using subjects from Australian Imaging, Biomarker & Lifestyle Flagship Study of Ageing (AIBL). We model the prototypical symptom trajectory classes using clinical assessment scores from mini-mental state exam (MMSE) and Alzheimer's Disease Assessment Scale (ADAS-13) at nine timepoints spanned over six years based on a hierarchical clustering approach. Subsequently we predict these trajectory classes for a given subject using magnetic resonance (MR) imaging, genetic, and clinical variables from two timepoints (baseline + follow-up). For prediction, we present a longitudinal Siamese neural-network (LSN) with novel architectural modules for combining multimodal data from two timepoints. The trajectory modeling yields two (stable and decline) and three (stable, slow-decline, fast-decline) trajectory classes for MMSE and ADAS-13 assessments, respectively. For the predictive tasks, LSN offers highly accurate performance with 0.900 accuracy and 0.968 AUC for binary MMSE task and 0.760 accuracy for 3-way ADAS-13 task on ADNI datasets, as well as, 0.724 accuracy and 0.883 AUC for binary MMSE task on replication AIBL dataset.
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spelling doaj.art-a6a9385954bc4ebe975eed99cdc6860a2022-12-22T03:49:24ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582018-09-01149e100637610.1371/journal.pcbi.1006376Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.Nikhil BhagwatJoseph D VivianoAristotle N VoineskosM Mallar ChakravartyAlzheimer’s Disease Neuroimaging InitiativeComputational models predicting symptomatic progression at the individual level can be highly beneficial for early intervention and treatment planning for Alzheimer's disease (AD). Individual prognosis is complicated by many factors including the definition of the prediction objective itself. In this work, we present a computational framework comprising machine-learning techniques for 1) modeling symptom trajectories and 2) prediction of symptom trajectories using multimodal and longitudinal data. We perform primary analyses on three cohorts from Alzheimer's Disease Neuroimaging Initiative (ADNI), and a replication analysis using subjects from Australian Imaging, Biomarker & Lifestyle Flagship Study of Ageing (AIBL). We model the prototypical symptom trajectory classes using clinical assessment scores from mini-mental state exam (MMSE) and Alzheimer's Disease Assessment Scale (ADAS-13) at nine timepoints spanned over six years based on a hierarchical clustering approach. Subsequently we predict these trajectory classes for a given subject using magnetic resonance (MR) imaging, genetic, and clinical variables from two timepoints (baseline + follow-up). For prediction, we present a longitudinal Siamese neural-network (LSN) with novel architectural modules for combining multimodal data from two timepoints. The trajectory modeling yields two (stable and decline) and three (stable, slow-decline, fast-decline) trajectory classes for MMSE and ADAS-13 assessments, respectively. For the predictive tasks, LSN offers highly accurate performance with 0.900 accuracy and 0.968 AUC for binary MMSE task and 0.760 accuracy for 3-way ADAS-13 task on ADNI datasets, as well as, 0.724 accuracy and 0.883 AUC for binary MMSE task on replication AIBL dataset.http://europepmc.org/articles/PMC6157905?pdf=render
spellingShingle Nikhil Bhagwat
Joseph D Viviano
Aristotle N Voineskos
M Mallar Chakravarty
Alzheimer’s Disease Neuroimaging Initiative
Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.
PLoS Computational Biology
title Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.
title_full Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.
title_fullStr Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.
title_full_unstemmed Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.
title_short Modeling and prediction of clinical symptom trajectories in Alzheimer's disease using longitudinal data.
title_sort modeling and prediction of clinical symptom trajectories in alzheimer s disease using longitudinal data
url http://europepmc.org/articles/PMC6157905?pdf=render
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