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

被引:6
|
作者
Wang, Ming [1 ]
Li, Zheng [1 ]
Lee, Eun Young [2 ]
Lewis, Mechelle M. [2 ]
Zhang, Lijun [3 ,4 ]
Sterling, Nicholas W. [2 ]
Wagner, Daymond [2 ]
Eslinger, Paul [1 ,2 ]
Du, Guangwei [2 ]
Huang, Xuemei [2 ,5 ,6 ,7 ,8 ]
机构
[1] Penn State Univ, Hershey Med Ctr, Dept Publ Hlth Sci, Hershey, PA 17033 USA
[2] Penn State Univ, Hershey Med Ctr, Dept Neurol, Hershey, PA 17033 USA
[3] Penn State Univ, Hershey Med Ctr, Dept Biochem & Mol Biol, Hershey, PA 17033 USA
[4] Penn State Univ, Hershey Med Ctr, Inst Personalized Med, Hershey, PA 17033 USA
[5] Penn State Univ, Hershey Med Ctr, Dept Pharmacol, Hershey, PA 17033 USA
[6] Penn State Univ, Hershey Med Ctr, Dept Radiol, Hershey, PA 17033 USA
[7] Penn State Univ, Hershey Med Ctr, Dept Neurosurg, Hershey, PA 17033 USA
[8] Penn State Univ, Hershey Med Ctr, Dept Kinesiol, Hershey, PA 17033 USA
关键词
Parkinson's disease; Multivariate longitudinal data; Generalized linear mixed-effect model; Dynamic prediction; Motor symptoms; Non-motor symptoms; Imbalance; COGNITIVE IMPAIRMENTS; R PACKAGE; MOTOR;
D O I
10.1186/s12874-017-0415-4
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
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 similar to 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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页数:10
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