Apathy in rapid eye movement sleep behaviour disorder is common and under-recognized
- PMID: 29114969
- PMCID: PMC5838543
- DOI: 10.1111/ene.13515
Apathy in rapid eye movement sleep behaviour disorder is common and under-recognized
Abstract
Background and purpose: Apathy is an important neuropsychiatric feature of Parkinson's disease (PD), which often emerges before the onset of motor symptoms. Patients with rapid eye movement sleep behaviour disorder (RBD) have a high probability of developing PD in future. Neuropsychiatric problems are common in RBD, but apathy has not previously been detailed in this key prodromal population.
Methods: Eighty-eight patients with polysomnographically proven RBD, 65 patients with PD and 33 controls were assessed for apathy using the Lille Apathy Rating Scale. Cognition and depression were also quantified. The sensitivity of the Unified Parkinson's Disease Rating Scale screening questions for apathy and depression was calculated.
Results: A total of 46% of patients with RBD were apathetic, compared with 31% of patients with PD in our sample. Most patients with RBD with depression were apathetic but more than half of apathetic patients were not depressed. The sensitivity of the single Unified Parkinson's Disease Rating Scale screening question was only 33% for mild apathy and 50% for severe apathy.
Conclusions: Apathy is common in RBD and is underestimated by a single self-report question. Recognition of apathy as a distinct neuropsychiatric feature in RBD could aid targeted treatment interventions and might contribute to the understanding of prodromal PD.
Keywords: Parkinson's disease; apathy; prodromal; rapid eye movement sleep behaviour disorder.
© 2017 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.
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Comment in
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Take care to identify apathy in idiopathic rapid eye movement sleep behavior disorder.Eur J Neurol. 2018 Jul;25(7):903-904. doi: 10.1111/ene.13627. Epub 2018 Apr 19. Eur J Neurol. 2018. PMID: 29528541 No abstract available.
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