4.4 Article

Accelerating diagnosis of Parkinson's disease through risk prediction

Journal

BMC NEUROLOGY
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12883-021-02226-4

Keywords

Parkinson’ s disease; Predictive medicine; Prodromal; Prediagnostic; Tremor; Gait

Funding

  1. Sanofi Aventis
  2. National Institute of Neurological Disorders and Stroke award [K99NS114850]
  3. NVIDIA Graduate Fellowship
  4. U.S. National Library of Medicine award [T15LM007092]

Ask authors/readers for more resources

This study explores the characterization of prediagnostic Parkinson's Disease and constructs a prediction model using machine learning, which not only identifies novel features but also allows for guiding clinical decisions and the possibility of earlier diagnosis for disease modifying therapies in clinical trials.
Background Characterization of prediagnostic Parkinson's Disease (PD) and early prediction of subsequent development are critical for preventive interventions, risk stratification and understanding of disease pathology. This study aims to characterize the role of the prediagnostic period in PD and, using selected features from this period as novel interception points, construct a prediction model to accelerate the diagnosis in a real-world setting. Methods We constructed two sets of machine learning models: a retrospective approach highlighting exposures up to 5 years prior to PD diagnosis, and an alternative model that prospectively predicted future PD diagnosis from all individuals at their first diagnosis of a gait or tremor disorder, these being features that appeared to represent the initiation of a differential diagnostic window. Results We found many novel features captured by the retrospective models; however, the high accuracy was primarily driven from surrogate diagnoses for PD, such as gait and tremor disorders, suggesting the presence of a distinctive differential diagnostic period when the clinician already suspected PD. The model utilizing a gait/tremor diagnosis as the interception point, achieved a validation AUC of 0.874 with potential time compression to a future PD diagnosis of more than 300 days. Comparisons of predictive diagnoses between the prospective and prediagnostic cohorts suggest the presence of distinctive trajectories of PD progression based on comorbidity profiles. Conclusions Overall, our machine learning approach allows for both guiding clinical decisions such as the initiation of neuroprotective interventions and importantly, the possibility of earlier diagnosis for clinical trials for disease modifying therapies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available