Optimising classification of Parkinson’s disease based on motor, olfactory, neuropsychiatric and sleep features

• Published in: NPJ Parkinson's Disease 2021-09, Vol.7 (1), p.87-87, Article 87
• Main Authors: Bestwick, Jonathan P., Auger, Stephen D., Schrag, Anette E., Grosset, Donald G., Kanavou, Sofia, Giovannoni, Gavin, Lees, Andrew J., Cuzick, Jack, Noyce, Alastair J.
• Format: Article
• Language: English
• Subjects: 692/499; 692/53/2423; Anxiety; Biomedical and Life Sciences; Biomedicine; Classification; Neurology; Neurosciences; Parkinson's disease; REM sleep
• ISSN: 2373-8057; 2373-8057
• DOI: 10.1038/s41531-021-00226-2

Olfactory loss, motor impairment, anxiety/depression, and REM-sleep behaviour disorder (RBD) are prodromal Parkinson’s disease (PD) features. PD risk prediction models typically dichotomize test results and apply likelihood ratios (LRs) to scores above and below cut-offs. We investigate whether LRs for specific test values could enhance classification between PD and controls. PD patient data on smell (UPSIT), possible RBD (RBD Screening Questionnaire), and anxiety/depression (LADS) were taken from the Tracking Parkinson’s study ( n  = 1046). For motor impairment (BRAIN test) in PD cases, published data were supplemented ( n  = 87). Control data (HADS for anxiety/depression) were taken from the PREDICT-PD pilot study ( n  = 1314). UPSIT, RBDSQ, and anxiety/depression data were analysed using logistic regression to determine which items were associated with PD. Gaussian distributions were fitted to BRAIN test scores. LRs were calculated from logistic regression models or score distributions. False-positive rates (FPRs) for specified detection rates (DRs) were calculated. Sixteen odours were associated with PD; LRs for this set ranged from 0.005 to 5511. Six RBDSQ and seven anxiety/depression questions were associated with PD; LRs ranged from 0.35 to 69 and from 0.002 to 402, respectively. BRAIN test LRs ranged from 0.16 to 1311. For a 70% DR, the FPR was 2.4% for the 16 odours, 4.6% for anxiety/depression, 16.0% for the BRAIN test, and 20.0% for the RBDSQ. Specific selections of (prodromal) PD marker features rather than dichotomized marker test results optimize PD classification. Such optimized classification models could improve the ability of algorithms to detect prodromal PD; however, prospective studies are needed to investigate their value for PD-prediction models.