Abstract

IntroductionParkinson’s disease (PD) patients in chronic levodopa treatment may experience motor and non-motor fluctuations, which may affect their quality of life. Safinamide is a new monoamine oxidase B inhibitor, also exerting a non-dopaminergic effect, recently approved as add-on therapy in fluctuating PD patients.MethodsWe performed a longitudinal prospective study in a cohort of 20 fluctuating PD patients, to test whether safinamide 50 mg may improve non-motor, cognitive, and behavioral symptoms over a 6-month treatment period. At each timepoint, clinical features were assessed by means of validated PD-specific scales. Neuropsychological assessment was performed by exploring all five cognitive domains.ResultsCompared to baseline, significant improvement was found in PD patients at 6-month follow-up in items investigating interest (p = 0.02), motivation (p = 0.02), and urinary disturbances (p = 0.03). Moreover, neuropsychiatric assessment showed a significant decrease in fatigue and apathy scores (p = 0.02 and p = 0.01, respectively). Motor assessment revealed a significant reduction in the total wake-up time spent in OFF state (p = 0.01). Follow-up neuropsychological evaluation did not reveal any change compared to baseline.ConclusionsOur data reveal that, along with motor fluctuation improvement, treatment with safinamide 50 mg may significantly decrease non-motor symptom burden in PD patients. Interestingly, non-dopaminergic mechanisms, such as glutamatergic overdrive, have been demonstrated to play a role in many pathways underlying these symptoms. Thus, we hypothesize that the neurotransmitter receptor-binding profile of safinamide may explain our findings.

Highlights

  • Parkinson’s disease (PD) patients in chronic levodopa treatment may experience motor and non-motor fluctuations, which may affect their quality of life

  • 20 fluctuating PD patients were enrolled in the study and after add-on with safinamide 50 mg performed a 6-month extensive follow-up

  • Eleven out of 20 PD patients were taking rasagiline as iMAO-B prior to the inclusion in this study; they were switched on safinamide

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Summary

Introduction

Parkinson’s disease (PD) patients in chronic levodopa treatment may experience motor and non-motor fluctuations, which may affect their quality of life. Parkinson’s disease (PD) is a common and complex neurodegenerative disorder characterized by motor features, such as slowness of movement, rigidity, and resting tremor as well as several and heterogenous non-motor symptoms This may be related to the fact that their neuroanatomical correlates in PD remain largely undefined, with limited insights for treatment options. Complications of long-term dopaminergic treatment are motor and non-motor fluctuations and dyskinesia, which can impair patients’ quality of life [4].

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