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Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model

BACKGROUND: It is challenging for current statistical models to predict clinical progression of Parkinson’s disease (PD) because of the involvement of multi-domains and longitudinal data. METHODS: Past univariate longitudinal or multivariate analyses from cross-sectional trials have limited power to...

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Autores principales: Wang, Ming, Li, Zheng, Lee, Eun Young, Lewis, Mechelle M., Zhang, Lijun, Sterling, Nicholas W., Wagner, Daymond, Eslinger, Paul, Du, Guangwei, Huang, Xuemei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613469/
https://www.ncbi.nlm.nih.gov/pubmed/28946857
http://dx.doi.org/10.1186/s12874-017-0415-4
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author Wang, Ming
Li, Zheng
Lee, Eun Young
Lewis, Mechelle M.
Zhang, Lijun
Sterling, Nicholas W.
Wagner, Daymond
Eslinger, Paul
Du, Guangwei
Huang, Xuemei
author_facet Wang, Ming
Li, Zheng
Lee, Eun Young
Lewis, Mechelle M.
Zhang, Lijun
Sterling, Nicholas W.
Wagner, Daymond
Eslinger, Paul
Du, Guangwei
Huang, Xuemei
author_sort Wang, Ming
collection PubMed
description BACKGROUND: It is challenging for current statistical models to predict clinical progression of Parkinson’s disease (PD) because of the involvement of multi-domains and longitudinal data. METHODS: Past univariate longitudinal or multivariate analyses from cross-sectional trials have limited power to predict individual outcomes or a single moment. The multivariate generalized linear mixed-effect model (GLMM) under the Bayesian framework was proposed to study multi-domain longitudinal outcomes obtained at baseline, 18-, and 36-month. The outcomes included motor, non-motor, and postural instability scores from the MDS-UPDRS, and demographic and standardized clinical data were utilized as covariates. The dynamic prediction was performed for both internal and external subjects using the samples from the posterior distributions of the parameter estimates and random effects, and also the predictive accuracy was evaluated based on the root of mean square error (RMSE), absolute bias (AB) and the area under the receiver operating characteristic (ROC) curve. RESULTS: First, our prediction model identified clinical data that were differentially associated with motor, non-motor, and postural stability scores. Second, the predictive accuracy of our model for the training data was assessed, and improved prediction was gained in particularly for non-motor (RMSE and AB: 2.89 and 2.20) compared to univariate analysis (RMSE and AB: 3.04 and 2.35). Third, the individual-level predictions of longitudinal trajectories for the testing data were performed, with ~80% observed values falling within the 95% credible intervals. CONCLUSIONS: Multivariate general mixed models hold promise to predict clinical progression of individual outcomes in PD. TRIAL REGISTRATION: The data was obtained from Dr. Xuemei Huang’s NIH grant R01 NS060722, part of NINDS PD Biomarker Program (PDBP). All data was entered within 24 h of collection to the Data Management Repository (DMR), which is publically available (https://pdbp.ninds.nih.gov/data-management).
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spelling pubmed-56134692017-10-11 Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model Wang, Ming Li, Zheng Lee, Eun Young Lewis, Mechelle M. Zhang, Lijun Sterling, Nicholas W. Wagner, Daymond Eslinger, Paul Du, Guangwei Huang, Xuemei BMC Med Res Methodol Research Article BACKGROUND: It is challenging for current statistical models to predict clinical progression of Parkinson’s disease (PD) because of the involvement of multi-domains and longitudinal data. METHODS: Past univariate longitudinal or multivariate analyses from cross-sectional trials have limited power to predict individual outcomes or a single moment. The multivariate generalized linear mixed-effect model (GLMM) under the Bayesian framework was proposed to study multi-domain longitudinal outcomes obtained at baseline, 18-, and 36-month. The outcomes included motor, non-motor, and postural instability scores from the MDS-UPDRS, and demographic and standardized clinical data were utilized as covariates. The dynamic prediction was performed for both internal and external subjects using the samples from the posterior distributions of the parameter estimates and random effects, and also the predictive accuracy was evaluated based on the root of mean square error (RMSE), absolute bias (AB) and the area under the receiver operating characteristic (ROC) curve. RESULTS: First, our prediction model identified clinical data that were differentially associated with motor, non-motor, and postural stability scores. Second, the predictive accuracy of our model for the training data was assessed, and improved prediction was gained in particularly for non-motor (RMSE and AB: 2.89 and 2.20) compared to univariate analysis (RMSE and AB: 3.04 and 2.35). Third, the individual-level predictions of longitudinal trajectories for the testing data were performed, with ~80% observed values falling within the 95% credible intervals. CONCLUSIONS: Multivariate general mixed models hold promise to predict clinical progression of individual outcomes in PD. TRIAL REGISTRATION: The data was obtained from Dr. Xuemei Huang’s NIH grant R01 NS060722, part of NINDS PD Biomarker Program (PDBP). All data was entered within 24 h of collection to the Data Management Repository (DMR), which is publically available (https://pdbp.ninds.nih.gov/data-management). BioMed Central 2017-09-25 /pmc/articles/PMC5613469/ /pubmed/28946857 http://dx.doi.org/10.1186/s12874-017-0415-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Ming
Li, Zheng
Lee, Eun Young
Lewis, Mechelle M.
Zhang, Lijun
Sterling, Nicholas W.
Wagner, Daymond
Eslinger, Paul
Du, Guangwei
Huang, Xuemei
Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model
title Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model
title_full Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model
title_fullStr Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model
title_full_unstemmed Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model
title_short Predicting the multi-domain progression of Parkinson’s disease: a Bayesian multivariate generalized linear mixed-effect model
title_sort predicting the multi-domain progression of parkinson’s disease: a bayesian multivariate generalized linear mixed-effect model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613469/
https://www.ncbi.nlm.nih.gov/pubmed/28946857
http://dx.doi.org/10.1186/s12874-017-0415-4
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