Research overview
The text below is the source article’s original abstract under a verified reuse license. cc by
BackgroundMotor symptoms of Parkinson's disease (PD) patients affect their ability of daily activities. Identifying distinct trajectories of motor symptom progression in PD patients can facilitate long-term management.MethodsA total of 155 PD patients were acquired from the Parkinson's Disease Progression Marker Initiative (PPMI). Distinct longitudinal trajectory clusters of motor symptom progression in PD patients were identified by unsupervised self-organizing maps (SOMs), and baseline characteristics were compared among different clusters. Linear mixed-effect analysis was utilized to estimate the longitudinal courses of some cardinal motor symptoms among clusters, while survival analysis was used to compare time-to-clinical milestones within 5 years. The support vector machine (SVM) was built to predict patients' trajectory clusters, and its performance was evaluated through the mean area under the receiver-operating characteristic curve (mAUC), accuracy and macro F 1-score. Shapley values were calculated to interpret individual variability.ResultsThe optimal clusters by SOMs are 3. Cardinal motor symptoms of the progressive cluster worsened more rapidly, and this cluster is more likely to have impaired balance, loss of independence, sleep disturbance, and cognitive impairment within 5 years. The mAUC, accuracy, and macro F 1-score of multi-class SVM model were 0.8846, 0.7692, and 0.7778, respectively. An interactive web application was developed to predict the individual's trajectory cluster.ConclusionSubtyping motor symptom progression into different trajectories can improve patients' management. Using baseline data to predict which trajectory cluster a patient belongs to may help develop interventions.
Scientific assessment
Research question
Assess the question within the original study’s scope.
Methods & sample
Check the source article for study design and sample details.
Key findings
An editorially approved findings summary is not yet published for this record.
Limitations
Generalizability, bias and clinical meaning require separate assessment.
Methods, samples and clinical conclusions are not inferred from bibliographic metadata.