Motor Complications in Parkinson's Disease: Results from 3343 Patients Followed for up to 12 Years

Author:

Gandhi Sacha E.1ORCID,Zerenner Tanja2ORCID,Nodehi Anahita2,Lawton Michael A.2,Marshall Vicky3,Al‐Hajraf Falah45,Grosset Katherine A.1,Morris Huw R.6ORCID,Hu Michele T.4ORCID,Ben‐Shlomo Yoav2,Grosset Donald G.1

Affiliation:

1. School of Neuroscience and Psychology University of Glasgow Glasgow United Kingdom

2. Population Health Sciences, Bristol Medical School University of Bristol Bristol United Kingdom

3. Institute of Neurological Sciences Glasgow United Kingdom

4. Oxford Parkinson's Disease Centre, Nuffield Department of Clinical Neuroscience Oxford University Oxford United Kingdom

5. Department of Pharmacology and Toxicology, Faculty of Medicine Kuwait University Kuwait City Kuwait

6. Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology University College London London United Kingdom

Abstract

AbstractBackgroundMotor complications are well recognized in Parkinson's disease (PD), but their reported prevalence varies and functional impact has not been well studied.ObjectivesTo quantify the presence, severity, impact and associated factors for motor complications in PD.MethodsAnalysis of three large prospective cohort studies of recent‐onset PD patients followed for up to 12 years. The MDS‐UPDRS part 4 assessed motor complications and multivariable logistic regression tested for associations. Genetic risk score (GRS) for Parkinson's was calculated from 79 single nucleotide polymorphisms.Results3343 cases were included (64.7% male). Off periods affected 35.0% (95% CI 33.0, 37.0) at 4–6 years and 59.0% (55.6, 62.3) at 8–10 years. Dyskinesia affected 18.5% (95% CI 16.9, 20.2) at 4–6 years and 42.1% (38.7, 45.5) at 8–10 years. Dystonia affected 13.4% (12.1, 14.9) at 4–6 years and 22.8% (20.1, 25.9) at 8–10 years. Off periods consistently caused greater functional impact than dyskinesia. Motor complications were more common among those with higher drug doses, younger age at diagnosis, female gender, and greater dopaminergic responsiveness (in challenge tests), with associations emerging 2–4 years post‐diagnosis. Higher Parkinson's GRS was associated with early dyskinesia (0.026 ≤ P ≤ 0.050 from 2 to 6 years).ConclusionsOff periods are more common and cause greater functional impairment than dyskinesia. We confirm previously reported associations between motor complications with several demographic and medication factors. Greater dopaminergic responsiveness and a higher genetic risk score are two novel and significant independent risk factors for the development of motor complications.

Funder

Parkinson's UK

Publisher

Wiley

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