Impulse control disorders in Parkinson disease and RBD
Citation
Fahd Baig,Mark J. Kelly, A. Lawton, Claudio Ruffmann, Michal Rolinski, Johannes C. Klein, Thomas Barber, Christine Lo, Yoav Ben-Shlomo, David Okai, and Michele T. Hu, Neurology 2019;93:e675-e687.
Abstract
Objective
To describe the prevalence, natural history, and risk factors for impulse control behaviors
(ICBs) among people with Parkinson disease (PD), those with REM sleep behavior disorder
(RBD), and controls.
Methods
Participants with early PD (within 3.5 years of diagnosis), those with RBD, and controls were
clinically phenotyped and screened for ICBs longitudinally (with the Questionnaire for Impulsivity
in Parkinson’s Disease). ICB-positive individuals were invited for a semistructured
interview, repeated 1 year later. The severity of the ICB was assessed with the Parkinson’s
Impulse Control Scale. Multiple imputation and regression models were used to estimate ICB
prevalence and associations.
Results
Data from 921 cases of PD at baseline, 768 cases at 18 months, and 531 cases at 36 months were
included, with 21% to 25% screening positive for ICBs at each visit. Interviews of ICB screen–
positive individuals revealed that 10% met formal criteria for impulse control disorders (ICD),
while 33% had subsyndromal ICD (ICB symptoms without reaching the formal diagnostic
criteria for ICD). When these data were combined through the use of multiple imputation, the
prevalence of PD-ICB was estimated at 19.1% (95% confidence interval 10.1–28.2). On followup,
24% of cases of subsyndromal ICD had developed full symptoms of an ICD. PD-ICD was
associated with dopamine agonist use, motor complications, and apathy but not PD-RBD. ICD
prevalence in the RBD group (1%) was similar to that in controls (0.7%).
Conclusions
ICBs occur in 19.1% of patients with early PD, many persisting or worsening over time. RBD is
not associated with increased ICD risk. Psychosocial drivers, including mood and support
networks, affect severity.
Description
Supported by the NIHR
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