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Impact of SAfinamide on Depressive Symptoms in Parkinson's Disease Patients (SADness-PD Study): A Multicenter Retrospective Study

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TLDR
In this paper, the effects of safinamide on depression, motor symptoms, and the serotonin syndrome related to its co-administration with antidepressants in patients with Parkinson's disease (PD) were assessed.
Abstract
Background: We aimed to assess the effects of safinamide on depression, motor symptoms, and the serotonin syndrome related to its co-administration with antidepressants in patients with Parkinson’s disease (PD). Methods: We retrospectively analyzed the data of patients at 1 and 3 months of follow-up compared to baseline. Results: n = 82 (safinamide 50 mg = 22, 100 mg = 60, with antidepressants = 44). First, we found improvement in depression (Hamilton Depression Rating Scale: −6 ± 5.10 at 1 month and −7.27 ± 5.10 at 3 months, p < 0.0001; Patient Global Impression of Improvement Scale: 60.3% and 69.5% of patients at 1 and 3 months reported some improvement). Second, safinamide improved the daily life activities and motor symptoms/motor complications (Unified Parkinson’s Disease Rating Scale (UPDRS-II): −2.51 ± 6.30 and −2.47 ± 6.11 at 1 and 3 months, p < 0.0001; III: −3.58 ± 8.68 and −4.03 ± 8.95 at 1 and 3 months, p < 0.0001; IV: −0.61 ± 2.61 and −0.8 ± 2.53 at 1 and 3 months, p < 0.0001). Third, 7.31% and 8.53% of patients developed non-severe adverse events related to safinamide at 1 and 3 months. Serotonin syndrome was not observed in the patients treated with antidepressants; some isolated serotonin syndrome symptoms were reported. Conclusions: Safinamide could be useful for treating depression in PD; it was effective for motor symptoms and motor complications and safe even when co-administered with antidepressants.

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Journal ArticleDOI

The neuropsychiatry of Parkinson's disease: advances and challenges

TL;DR: In people with Parkinson's disease, neuropsychiatric signs and symptoms are common throughout the disease course and their presentation can be similar to, or distinct from, their counterparts in the general population as mentioned in this paper .
Journal ArticleDOI

The role of glutamatergic neurotransmission in the motor and non-motor symptoms in Parkinson's disease: Clinical cases and a review of the literature.

TL;DR: Safinamide has been used for fluctuating Parkinson's disease (PD) as add-on therapy to levodopa regimens for the management of ‘off’ episodes as mentioned in this paper.
Journal ArticleDOI

Silibinin ameliorates depression/anxiety-like behaviors of Parkinson's disease mouse model and is associated with attenuated STING-IRF3-IFN-β pathway activation and neuroinflammation.

TL;DR: In this paper, the authors reported that silibinin showed anti-depressant and anti-anxiety effects on 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced model mice with Parkinson's disease.
Journal ArticleDOI

Effectiveness of Safinamide over Mood in Parkinson's Disease Patients: Secondary Analysis of the Open-label Study SAFINONMOTOR.

TL;DR: The SAFINON MOTOR study as mentioned in this paper showed that SAFINamide improves mood in patients with Parkinson's disease at 6 months by reducing the BDI-II (Beck Depression Inventory-II), NMSS mood/apathy domain, and PDQ-39 (Parkinson’s Disease Questionnaire-39) emotional well-being domain.
References
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Journal ArticleDOI

Systematic review of levodopa dose equivalency reporting in Parkinson's disease

TL;DR: A systematic review of studies reporting LEDs yielded a standardized LED for each drug, providing a useful tool to express dose intensity of different antiparkinsonian drug regimens on a single scale.
Journal ArticleDOI

Depression in Parkinson disease—epidemiology, mechanisms and management

TL;DR: The frequency and course of depression in patients with Parkinson disease is described, the mechanisms that underlie depression in this disease are discussed, and the management strategies for these patients are highlighted.
Journal ArticleDOI

Glutamatergic Modulators: The Future of Treating Mood Disorders?

TL;DR: Evidence confirming the role of the glutamatergic modulators riluzole and ketamine as proof-of-concept agents in this system holds considerable promise for developing the next generation of novel therapeutics for the treatment of bipolar disorder and major depressive disorder.
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