Abstract
Background
Safinamide is a recent multimodal antiparkinsonian drug that inhibits monoamine oxidase B and modulates the glutamatergic system with positive effects on motor and nonmotor symptoms of Parkinson’s disease (PD). This post-hoc analysis of the European SYNAPSES study provides first-time data on the use of safinamide in routine clinical practice in Belgium.
Objective
To describe the efficacy and safety of safinamide in Belgian PD patients in real-life conditions.
Methods
Post-hoc analysis of the Belgian cohort from the European SYNAPSES trial, which was an observational, multicenter, retrospective-prospective cohort study. Patients were followed up to 12 months. Analyses were performed in the overall population and according to different criteria such as the age limit (> 75 years), presence or absence of relevant comorbidities, presence or absence of psychiatric conditions such as depression and anxiety, patients on levodopa monotherapy or levodopa in combination with other treatments, patients on rasagiline before inclusion or not.
Results
Of the 172 patients included, 29.2% were > 75 years, 58.9% had relevant comorbidities and 32.7% had psychiatric conditions. Almost all the patients reported motor (98.8%) or non-motor (86.3%) symptoms. During the study, 36.3% of patients reported drug-related reactions. The adverse drug reactions were those already described in the patients’ information leaflet. The majority were mild or moderate and completely resolved and no differences were detected between the subgroups of patients. Almost 35% of the patients demonstrated a clinically significant improvement in the UPDRS and 50% of the patients with wearing-off at baseline, did not report wearing-off anymore after one year of treatment. Patients under levodopa monotherapy compared to patients receiving levodopa combined with other antiparkinsonian treatments benefit more from safinamide treatment. Patients switched from rasagiline to safinamide seemed also to benefit more from safinamide treatment.
Conclusion
The study confirms the excellent safety and efficacy profile of safinamide, particularly in more vulnerable groups of patients such as the elderly and patients with significant comorbidities or psychiatric conditions such as depression or anxiety.
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Introduction
Safinamide is a recent treatment option for PD patients who experience motor fluctuations under levodopa. Safinamide is a highly selective and reversible monoamine oxidase inhibitor (MAO), with additional properties including blockage of voltage-dependent sodium channels, modulating calcium channels and inhibiting glutamate release [1, 2]. Its dual mechanism of action, dopaminergic (reversible monoamine oxidase-B inhibition) and non-dopaminergic (modulation of the abnormal glutamate release), offers an innovative approach for the management of motor and nonmotor symptoms and motor complications [3]. None of the drugs for PD already on the market have this peculiar double mechanism of action, therefore the Movement Disorder Society has included safinamide in a class of drugs different from selegiline and rasagiline [4]. Short and long-term placebo-controlled studies with safinamide have demonstrated enhanced symptom control of motor function in advanced PD [5,6,7]. Moreover, an anti-dyskinetic effect of safinamide has been shown in animal models [8] and clinical studies [9, 10]. Post-hoc analyses of the pivotal studies and post-registration studies indicate that safinamide might have a beneficial effect on nonmotor symptoms such as pain, sleep or depression, and improves several aspects of the quality of life [10,11,12,13,14,15,16].
Real-world evidence is essential and supplements data from randomized controlled trials by providing data from large populations, risk–benefit assessment, data on patient groups not previously studied and determining long-term outcomes. This potentially impacts on hypothesis generation, new drug indications and label expansion, and informs treatment guidelines.
Variations in symptoms or treatments across geographical regions have been described. For example, in a large population-based study, non-motor symptom score was highest in Europe and Americas whereas the scores for anxiety, depression or the quality of life was highest in Japan and India [17]. The PRISM study, which was a European survey of the burden of Parkinson’s disease in patients and their carers found that levodopa was the first prescribed anti-PD medication in 67.4%, ranging from 58.2% in France to 87.5% in Portugal. Levodopa was taken as monotherapy by 21.8% of the overall population, ranging from 8.3% in Germany to 38.3% in the United Kingdom [18].
Abbruzzese et al. [19] conducted a large European Drug Utilization Study called “SYNAPSES” (“European multicenter retrospective-prospective cohort StudY to observe safiNAmide safety profile and pattern of use in clinical Practice during the firSt post-commErcialization phaSe”). The primary objective of this study was to provide additional real-world data on safinamide treatment in some categories of patients not well represented in the pivotal clinical trials, namely those aged > 75, with relevant comorbidities and with concomitant psychiatric conditions as psychosis, bipolar disorder and severe depression.
The SYNAPSES study was conducted in 6 European countries (Belgium, Germany, Italy, Spain, Switzerland, and United Kingdom) and involved 128 neurology and geriatric centers specialized in PD treatment. A total of 1610 patients were enrolled, of which 25.1% were above 75 years, 70.8% had relevant comorbidities and 42.4% had psychiatric conditions. Patients were followed for 12 months after the start of treatment. 27.7% of patients reported adverse drug reactions. The majority of these events were mild or moderate and completely resolved and no differences were detected between the subgroups of patients. Clinically significant improvements were seen in the UPDRS motor score and the UPDRS total score in ≥ 40% of patients. Patients with motor fluctuations decreased by 40–50% at the end of the study.
Thirteen [13] Belgian sites participated and included 172 evaluable patients, corresponding to 10.7% of the global European cohort. Since previous studies have reported differences in Parkinson symptom and treatment profiles across countries, this post-hoc analysis aims to describe specifically the effectiveness and safety of safinamide in the Belgian cohort of the SYNAPSES study.
Materials and methods
Design and patients
The protocol and patient materials were approved by all the National and local Independent Ethics Committees and the study was conducted according to the ethical standards of the institutional and/or national research committee and according to the Declaration of Helsinki. We refer to the original publication of Abbruzzese et al. [19] for a detailed description of the study design. Briefly, in this open-label non-interventional real-life study, all male and female patients aged ≥ 18 years who started treatment with safinamide at the enrolment visit or in the preceding four months according to the product information, with signed informed and privacy consent forms were eligible to enter a 12 months follow-up treatment including 4 visits, each separated by 4 months. Physicians participating in the study received appropriate compensation.
Outcome measures
The post hoc analyses reported here are provided for the overall Belgian population. When the number of patients was sufficiently large, the data were further analyzed in the following subgroups: patients aged ≤ 75 vs. > 75, patients with or without relevant comorbidities, patients with or without psychiatric conditions, patients at entry with levodopa in monotherapy vs. levodopa in combination with other anti-parkinsonian drugs and patients previously treated with or without rasagiline. In addition, the following endpoints were evaluated: patient demographic and clinical characteristics, Parkinson’s disease treatment concomitant to safinamide and supportive psychiatric therapy, motor evaluation as measured by UPDRS III, total UPDRS score (subscales I, II, and III as defined by Shulman et al. [20] and motor complications, safety analysis.
Statistical methods
The statistical analysis was performed on all the Belgian evaluable patients for the Full Analysis Set (FAS) defined as the patients satisfying all inclusion criteria and not violating any exclusion criteria. Data collected on all patients were pooled for statistical analyses. Patients with missing values were not excluded from the analysis, but their data were not replaced; the frequency of missing data was given for all analyzed variables. Descriptive analyses were performed; quantitative variables were described by mean, standard deviation, median, 25th and 75th percentile, minimum and maximum, while categorical variables by absolute and relative frequency. Non-parametric Wilcoxon Rank-Sum Test for non-normally distributed numerical variables and Chi-square or Fisher test for categorical variables were performed to compare patients in subgroups of interest. SAS for Windows Version 9.4 and SAS Enterprise Guide 7.1 were used for statistical analyses.
Results
Demography
The patients’ characteristics are shown in Table 1. Out of the 172 patients enrolled, 168 (97.7%) were evaluable for the analysis, with 125 (72.7%) patients with 12-month follow-up data. Older-than-75-year patients were N = 49 (29.2%), patients with relevant comorbidities were N = 99 (58.9%) and patients with psychiatric conditions were N = 55 (32.7%). Hypertension and heart diseases, metabolic disorders and osteoarticular pain disorders represented most of the associated relevant comorbidities. The associated psychiatric conditions were mainly depression (18.5%) and anxiety (12.5%). Some patients reported apathy (N = 3), insomnia (N = 3), aggression (N = 1) or disinhibition (N = 1). The mean (SD) age was 69.6 years (10.7) with a majority of males (n = 102; 60.7%). The mean (SD) age at time of onset was 61.0 years (13.2) with a mean (SD) time from PD onset of symptoms of 8.4 (5.6) and a mean time to diagnosis of 7.6 (2.5) years. The mean Hoehn and Yahr (H&Y) stage was 2.3 (0.7) with a UPDRS Part III score of 20.3.
Figure 1 shows the motor and nonmotor symptoms at baseline. Virtually all (98.8%) the patients had motor symptoms, mostly bradykinesia 88.1%, rigidity 81.5% and tremor 53.6%. 86.3% reported nonmotor symptoms such as fatigue (45.2%), sleep disorders (38.1%), psychiatric symptoms (32.1%), pain (20.8%) and cognitive symptoms (19.6%).
Concomitant medications
All patients had at least one ongoing treatment for PD at the start of safinamide therapy. As shown in Table 2, 166 patients (98.8%) were treated with levodopa, 75 (44.6%) with dopamine agonists, 45 (26.8%) with catechol-O-methyltransferase inhibitors (COMT-I), 20 (11.9%) with amantadine and 7 (4.2%) with anticholinergics.
Patients younger than 75 years received more COMT-I (31.1 vs. 14.3%), dopamine agonists (56.3 vs. 16.3%) or anticholinergics (5.9 vs. 0%).
More than 20% of the patients were on antidepressant treatment, mainly selective serotonin reuptake inhibitors (SSRIs), 10.7% or serotonin-norepinephrine reuptake inhibitors (SNRIs).
Adverse drug reactions
Sixty-one patients (36.3%) experienced at least one adverse drug reaction. 80% of the adverse drug reactions were mild (41%) to moderate (39%) in severity. Adverse drug reactions were reported in 46 (38.7%) patients below 75 years compared to 15 patients (30.6%) above 75 years and in 41 (41.4%) and 20 (29.0%) patients with and without relevant comorbidities, respectively. These differences were not statistically different (p = 0.0993). Patients with psychiatric conditions reported more frequently adverse drug reactions (49.1 vs. 30.1%, p = 0.0162). The types of adverse drug reactions did not differ between the different subgroups. Dyskinesia was the most frequently reported adverse drug reaction in 18 patients (10.7%). Dyskinesias were mostly mild (56%) to moderate (33%) in severity and the majority (67%) did not lead to any action. Looking at the subgroups, patients with psychiatric conditions reported dyskinesias more frequently (16.4% vs. 8.0%). Other adverse reactions that were reported at least 4 times were dyspepsia or nausea (N = 7, 6.6%), somnolence (N = 5, 4.7%), malaise (N = 4, 3.8%) and hypertension (N = 4, 3.8%).
Few psychiatric events were reported as adverse drug reactions. Anxiety was reported in three, a confusional state in two, hallucinations in two, impulse behavior in one, depression in two, completed suicide in one and sleep disorder in two cases.
Two reports of hallucinations were identified as drug-related. One of which, occurring in a patient below 75, classified as mild in severity, resulted in permanent discontinuation.
Overall, 48 patients (28.6%) of the patients discontinued their treatment permanently. No relevant differences were noted between the different subgroups’ analyses. Adverse reactions (N = 18, 37.5%), patient choice (N = 13, 27.1%) and disease progression/lack of efficacy (N = 10, 20.8%) were the three main reasons for permanent discontinuation.
UPDRS Scores
The mean (SD) baseline and at 12-month follow-up UPDRS part III and total scores are shown in Table 3. The disease severity expressed in UPDRS part III and UPDRS total score remained stable over time. According to the criteria developed by Shulman [20], a difference > 4.3 points for the UPDRS Total Score and > 2.5 points for the UPDRS Part III (Motor Examination score) is considered clinically significant. The percentage of patients with clinically meaningful differences between baseline and 12-month follow-up visit is also reported in Table 3 After one year of treatment with safinamide, 34.6% and 26.5% of patients showed a clinically meaningful improvement in UPDRS Motor and Total scores, respectively.
Motor fluctuations
Most of the patients had motor complications at baseline (96.4%). Motor complications were frequently reported as wearing-off fluctuations (70.2%) and dyskinesia (45.8%). The percentage of patients with motor complications decreased rapidly as from the first follow-up visit at 4 months. After one year of treatment, the relative decrease in the percentage of patients with wearing-off fluctuations or dyskinesia was 50% and 27.9%, respectively (see Fig. 2).
Patients with levodopa in monotherapy compared to patients with levodopa in combination with other anti-PD treatment
Eighty patients (47.6%) were initially on levodopa monotherapy. Patients with levodopa in combination with other anti-parkinsonian treatments were younger, but the time from diagnosis or onset of symptoms to baseline was longer than for the patients on levodopa only. The mean H&Y stage was higher in the group of patients with levodopa in combination. 27% of the patients on levodopa monotherapy had H&Y stage > 2 (N = 16), the proportion was 45% in patients with levodopa in combination (N = 29). Both treatment groups had comparable baseline UPDRS III and total scores (Table 4).
Irrespective of whether the patients received safinamide on top of levodopa monotherapy or levodopa in combination, around 34% and 25% of the patients had a clinically meaningful improvement of the UPDRS motor or UPDRS total scores at the end of the 12 months follow-up period.
Significantly more patients with levodopa in combination compared to the group of patients with levodopa in monotherapy reported dyskinesia at baseline (64.2 vs. 31.6%, p = 0.0003) and at the end of the 12 months follow-up (43.3 vs. 26.3%, p = 0.0491).
Although around 36% of the patients, irrespective of the concomitant treatment, reported at least one adverse drug reaction, severe adverse drug reactions seemed to occur more frequently in patients with levodopa in combination (15 vs. 3).
Patients previously treated with rasagiline
23 patients (13.7%) were receiving a MAOB-I (rasagiline) prior to inclusion. To be included in the study, patients needed to discontinue their MAOB-I treatment as indicated by the manufacturer. At inclusion, patients previously treated with rasagiline were more likely to be younger than 75 years (N = 19, 16 vs. N = 4, 8.2%). There were no significant differences in the baseline UPDRS motor or total score and they remained stable throughout the whole follow-up period. Wearing-off fluctuations were reported at baseline in a comparable percentage of patients (with rasagiline: 56.5%, without rasagiline: 72.4%, p = 0.1215). At the end of the 12 month of safinamide treatment, significantly fewer patients who were previously on rasagiline still reported wearing-off fluctuations compared to those who had not previously been on rasagiline (12.5 vs. 42.2% p = 0.0271).
Around 96% and 70% of the patients reported any type of motor complications or wearing-off fluctuations at baseline, irrespective of whether they were previously receiving rasagiline. However, at the end of the 12-month follow-up period, fewer patients who were prior to inclusion on rasagiline compared to patients not on rasagiline continued to report any type of motor complications (37.5 vs. 70.6%; p value 0.0203) or wearing-off fluctuations (12.5 vs. 42.2%; p value 0.0271) in particular.
The number of patients with at least one adverse drug reaction was comparable amongst the two treatment groups (previously on rasagiline: N = 6, 26.1% vs. not previously on rasagiline: N = 55, 37.9%).
Discussion
This post-hoc analysis of the large European SYNAPSES study provides long-term real-life data on the use of safinamide in a representative Belgian Parkinson’s disease population. This analysis confirms the benefit of safinamide, also in specific populations such as patients older than 75 years, patients with relevant comorbidities or psychiatric conditions, such as depression and anxiety. No major or unexpected safety concerns were identified.
As previously reported, we also found differences in the patient and treatment profiles of the Belgian cohort compared to the full set of European patients included in the SYNAPSES study. Belgian patients reported less relevant comorbidities (58.9 vs. 70.8%) or psychiatric conditions (32.7 vs. 42.4%), and lower UPDRS III (20.3 vs. 25.6) and UPDRS Total scores (38.1 vs. 43.5). Finally, Belgian patients were less likely to receive dopamine agonists (44.6 vs. 58.5%). These differences might be indicative of differences in the management approaches across countries.
As expected with drugs that increase levodopa bioavailability [21], the most frequently reported adverse event was dyskinesias. However, the incidence was lower compared to the observed frequency in previous pivotal clinical trials and was primarily mild to moderate with no clinically relevant consequences. Interestingly, more than 45% of the patients reported dyskinesias at the beginning of the study. However, after 12 months of follow-up nearly 30% of these patients did not report dyskinesias anymore. Even better results were obtained for wearing-off fluctuations, whereas 50% of the patients who reported wearing-off fluctuations did not report these complications at the end of the 12 months follow-up.
The overall incidence of patients reporting nonmotor symptoms was very high in the study. Previous clinical observations with safinamide demonstrated its potential in improving nonmotor symptoms such as pain [14, 15], sleep [16] or mood [15, 22]. The favorable effect of safinamide on these symptoms may be explained by its dopaminergic effect and its inhibitory action on state- and use-dependent sodium channels and abnormal glutamate release [23].
In our study, 9.5% of the patients had major depression according to the investigator’s judgment. Vanderheyden et al. [24] evaluated in the large scale PARKIDEP survey the prevalence of major depression in a Belgian Parkinson’s disease representative population and found a prevalence of 15.6% according to the MINI questionnaire. This percentage was similar to that of 17% found by the systematic review from Reijnders [25]. The low prevalence of major depression reported in our study compared to others might indicate the underdiagnosis of severe comorbid psychiatric conditions and the importance of integrating some screening tools to manage the disease.
More than one-third (34.6%) of the patients showed a clinically meaningful improvement of their UPDRS motor score after 1 year of treatment. This percentage is lower than the 45% of patients that reached the same improvement in the International Synapses study. The UPDRS scores at baseline can explain this difference, significantly higher in the European study (25.6) than the Belgian cohort (20.3).
Motor complications, particularly wearing-off and early morning fluctuations, affect most patients with PD. As observed in the DEEP study, 63–75.6% of patients treated with l-dopa experienced wearing-off with a significant deterioration of their quality of life [26]. The pharmacological treatment of motor fluctuations is difficult and remains a real unmet need [27]. Safinamide was shown to reduce by 40–50% the number of patients reporting motor complications such as wearing-off, early morning fluctuations, delayed-on. The number of patients reporting dyskinesias was decreased by 27.9%.
Around half of the patients were on levodopa combination therapy at baseline, mostly dopamine agonists (44.6%) or COMT-I (26.8%). In a previous post-hoc analysis performed by Cattaneo et al. [10], patients receiving safinamide 100 mg for 6 months had a mean OFF-time decrease vs. placebo of 1.35 h for those on levodopa monotherapy compared to 0.81 h for those on levodopa combination therapy. Although this requires further confirmation in a randomized clinical study, these data suggest that safinamide can be seen as a first line levodopa add-on treatment.
This post-hoc analysis also provides information on patients who were previously receiving rasagiline and who switched to safinamide. Although comparable percentages of patients previously under rasagiline or rasagiline-naïve patients reported wearing-off fluctuations at baseline (56.5% and 72.4%), 78% of the patients previously reporting wearing-off under rasagiline reported no more wearing-off fluctuations after 1-year safinamide treatment. This beneficial effect of safinamide was more significant than for the rasagiline naive patients that decreased by 42% (p = 0.0271). The pathophysiology of motor complications such as the wearing-off phenomenon remains poorly understood [28, 29]. Finely regulated interaction between dopamine and glutamate receptors appears essential to the normal physiology of the medium spiny output neurons and the basal ganglia. As reported by Calon and al. [30], glutamate receptor supersensitivity in the putamen seems to play a role in developing motor complications following long-term levodopa therapy in PD. The observed significant decrease in the percentage of patients previously treated with rasagiline not reporting wearing-off after safinamide treatment might be related to the glutamatergic modulating activity of safinamide in addition to its highly selective MAO-B inhibition.
This publication has several limitations: the open-label design without a placebo or active control, the post-hoc analyses, and the low number of evaluable patients for some specific analyses.
Conclusions
This post-hoc analysis of the SYNAPSES study provides long-term real life clinical data on the use of safinamide in a Belgian population of Parkinson’s disease patients. The favorable safety profile of safinamide was confirmed in the three subpopulations, namely patients above 75 years, with relevant comorbidities or with psychiatric conditions such as depression and anxiety. One-third of the patients experienced a clinically meaningful improvement in the UPDRS motor score after 1 year of treatment. This was accompanied by a 27.9–50.0% decrease in patients reporting motor complications. Although safinamide decreased the reported dyskinesias strongly after 1 year of treatment, this type of motor complication remained more frequent in patients treated with levodopa in combination with other anti-parkinsonian drugs compared to levodopa in monotherapy. Finally, patients who switched from rasagiline reported less wearing-off fluctuations than those previously not on rasagiline. These new clinical data confirm the excellent safety profile of safinamide in even more susceptible populations and support the unique glutamatergic modulating effect on motor complications.
Limitations
The limitations of this study include the limited number of patients in some subgroups that may have influenced or confounded the conclusions. In addition, no statistical comparison was provided between the original Synapses cohort and the Belgian cohort. Finally, no information was provided to ensure that the improvement in motor UPDRS and motor complications is directly attributed to safinamide.
References
Onofrj M, Bonanni L, Thomas A (2008) An expert opinion on safinamide in Parkinson’s disease. Expert Opin Investig Drugs 17(7):1115–1125. https://doi.org/10.1517/13543784.17.7.1115 (PMID: 18549347)
Caccia C, Maj R, Calabresi M, Maestroni S, Faravelli L, Curatolo L, Salvati P, Fariello RG (2006) Safinamide: from molecular targets to a new anti-Parkinson drug. Neurology 67(7 Suppl 2):S18-23. https://doi.org/10.1212/wnl.67.7_suppl_2.s18 (PMID: 17030736)
Müller T, Foley P (2017) Clinical pharmacokinetics and pharmacodynamics of safinamide. Clin Pharmacokinet 56(3):251–261. https://doi.org/10.1007/s40262-016-0449-5 (PMID: 27665574)
Fox SH, Katzenschlager R, Lim SY, Barton B, de Bie RMA, Seppi K, Coelho M, Sampaio C, Movement Disorder Society Evidence-Based Medicine Committee (2018) International Parkinson and Movement Disorder Society evidence-based medicine review: update on treatments for the motor symptoms of Parkinson’s disease. Mov Disord 33(8):1248–1266. https://doi.org/10.1002/mds.27372 (Epub 2018 Mar 23. Erratum in: Mov Disord. 2018 Dec;33(12):1992. PMID: 29570866)
Borgohain R, Szasz J, Stanzione P, Meshram C, Bhatt M, Chirilineau D, Stocchi F, Lucini V, Giuliani R, Forrest E, Rice P, Anand R, Study 016 Investigators (2014) Randomized trial of safinamide add-on to levodopa in Parkinson’s disease with motor fluctuations. Mov Disord 29(2):229–237. https://doi.org/10.1002/mds.25751 (Epub 2013 Dec 9. PMID: 24323641; PMCID: PMC4285943)
Borgohain R, Szasz J, Stanzione P, Meshram C, Bhatt MH, Chirilineau D, Stocchi F, Lucini V, Giuliani R, Forrest E, Rice P, Anand R, Study 018 Investigators (2014) Two-year, randomized, controlled study of safinamide as add-on to levodopa in mid to late Parkinson’s disease. Mov Disord 29(10):1273–1280. https://doi.org/10.1002/mds.25961
Schapira AH, Fox SH, Hauser RA, Jankovic J, Jost WH, Kenney C, Kulisevsky J, Pahwa R, Poewe W, Anand R (2017) Assessment of safety and efficacy of safinamide as a levodopa adjunct in patients with Parkinson disease and motor fluctuations: a randomized clinical trial. JAMA Neurol 74(2):216–224. https://doi.org/10.1001/jamaneurol.2016.4467 (PMID: 27942720)
Grégoire L, Jourdain VA, Townsend M, Roach A, Di Paolo T (2013) Safinamide reduces dyskinesias and prolongs L-DOPA antiparkinsonian effect in parkinsonian monkeys. Parkinsonism Relat Disord 19(5):508–514. https://doi.org/10.1016/j.parkreldis.2013.01.009 (Epub 2013 Feb 9 PMID: 23402994)
Cattaneo C, Ferla RL, Bonizzoni E, Sardina M (2015) Long-Term effects of safinamide on dyskinesia in mid- to late-stage Parkinson’s disease: a post-hoc analysis. J Parkinsons Dis 5(3):475–481. https://doi.org/10.3233/JPD-150569
Cattaneo C, Sardina M, Bonizzoni E (2016) Safinamide as add-on therapy to levodopa in mid- to late-stage Parkinson’s disease fluctuating patients: post hoc analyses of studies 016 and SETTLE. J Parkinsons Dis 6(1):165–173. https://doi.org/10.3233/JPD-150700.PMID:26889632;PMCID:PMC4927927
Bonuccelli U (2015) Effects of safinamide on motor complications and pain in advancing Parkinson’s disease – post hoc analyses of pivotal trials. Eur Neurol Rev 10(2):176–181
Cattaneo C, Barone P, Bonizzoni E, Sardina M (2017) Effects of safinamide on pain in fluctuating Parkinson’s disease patients: a post-hoc analysis. J Parkinsons Dis 7(1):95–101. https://doi.org/10.3233/JPD-160911
Cattaneo C, Kulisevsky J, Tubazio V, Castellani P (2018) Long-term efficacy of safinamide on Parkinson’s disease chronic pain. Adv Ther 35(4):515–522. https://doi.org/10.1007/s12325-018-0687-z
Geroin C, Di Vico IA, Squintani G, Segatti A, Bovi T, Tinazzi M (2020) Effects of safinamide on pain in Parkinson’s disease with motor fluctuations: an exploratory study. J Neural Transm (Vienna) 127(8):1143–1152. https://doi.org/10.1007/s00702-020-02218-7 (Epub 2020 Jun 22 PMID: 32572581)
Cattaneo C, Müller T, Bonizzoni E, Lazzeri G, Kottakis I, Keywood C (2017) Long-term effects of safinamide on mood fluctuations in Parkinson’s disease. J Parkinsons Dis 7(4):629–634. https://doi.org/10.3233/JPD-171143.PMID:28777756;PMCID:PMC5676861
Liguori C, Stefani A, Ruffini R, Mercuri NB, Pierantozzi M (2018) Safinamide effect on sleep disturbances and daytime sleepiness in motor fluctuating Parkinson’s disease patients: a validated questionnaires-controlled study. Parkinsonism Relat Disord 57:80–81. https://doi.org/10.1016/j.parkreldis.2018.06.033 (Epub 2018 Jun 30 PMID: 30006034)
van Wamelen DJ, Sauerbier A, Leta V, Rodriguez-Blazquez C, Falup-Pecurariu C, Rodriguez-Violante M, Rizos A, Tsuboi Y, Metta V, Bhidayasiri R, Bhattacharya K, Borgohain R, Prashanth LK, Rosales R, Lewis S, Fung V, Behari M, Goyal V, Kishore A, Lloret SP, Martinez-Martin P, Chaudhuri KR (2021) Cross-sectional analysis of the Parkinson’s disease Non-motor International Longitudinal Study baseline non-motor characteristics, geographical distribution and impact on quality of life. Sci Rep 11(1):9611. https://doi.org/10.1038/s41598-021-88651-4
Tolosa E, Ebersbach G, Ferreira JJ, Rascol O, Antonini A, Foltynie T, Gibson R, Magalhaes D, Rocha JF, Lees A (2021) The Parkinson’s Real-World Impact Assessment (PRISM) Study: a European survey of the burden of Parkinson’s disease in patients and their carers. J Parkinsons Dis 11(3):1309–1323. https://doi.org/10.3233/JPD-212611
Abbruzzese G, Kulisevsky J, Bergmans B, Gomez-Esteban JC, Kägi G, Raw J, Stefani A, Warnecke T, Jost WH, SYNAPSES Study Investigators Group (2021) A European observational study to evaluate the safety and the effectiveness of safinamide in routine clinical practice: the SYNAPSES trial. J Parkinsons Dis. https://doi.org/10.3233/JPD-219007 (Erratum for: J Parkinsons Dis. 2021;11(1):187–198. PMID: 34275911)
Shulman LM, Gruber-Baldini AL, Anderson KE, Fishman PS, Reich SG, Weiner WJ (2010) The clinically important difference on the unified Parkinson’s disease rating scale. Arch Neurol 67(1):64–70. https://doi.org/10.1001/archneurol.2009.295 (PMID: 20065131)
Freitas ME, Hess CW, Fox SH (2017) Motor complications of dopaminergic medications in Parkinson’s disease. Semin Neurol 37(2):147–157. https://doi.org/10.1055/s-0037-1602423
Peña E, Borrué C, Mata M, Martínez-Castrillo JC, Alonso-Canovas A, Chico JL, López-Manzanares L, Llanero M, Herreros-Rodríguez J, Esquivel A, Maycas-Cepeda T, Ruíz-Huete C (2021) Impact of SAfinamide on depressive symptoms in Parkinson’s disease patients (SADness-PD Study): a multicenter retrospective study. Brain Sci 11(2):232. https://doi.org/10.3390/brainsci11020232
Pisanò CA, Brugnoli A, Novello S, Caccia C, Keywood C, Melloni E, Vailati S, Padoani G, Morari M (2020) Safinamide inhibits in vivo glutamate release in a rat model of Parkinson’s disease. Neuropharmacology 167:108006. https://doi.org/10.1016/j.neuropharm.2020.108006
Vanderheyden JE, Gonce M, Bourgeois P, Cras P, De Nayer AR, Flamez A, Supiot F, Donneau AF, Albert A, Berlaimont V, PARKIDEP Investigators Group (2010) Epidemiology of major depression in Belgian Parkinsonian patients. Acta Neurol Belg 110(2):148–156
Reijnders JS, Ehrt U, Weber WE, Aarsland D, Leentjens AF (2008) A systematic review of prevalence studies of depression in Parkinson’s disease. Mov Disord 23(2):183–189. https://doi.org/10.1002/mds.21803
Stocchi F, Antonini A, Barone P, Tinazzi M, Zappia M, Onofrj M, Ruggieri S, Morgante L, Bonuccelli U, Lopiano L, Pramstaller P, Albanese A, Attar M, Posocco V, Colombo D, Abbruzzese G, DEEP Study Group (2014) Early DEtection of wEaring off in Parkinson disease: the DEEP study. Parkinsonism Relat Disord 20(2):204–211. https://doi.org/10.1016/j.parkreldis.2013.10.027 (Epub 2013 Nov 5. Erratum in: Parkinsonism Relat Disord. 2015 Jul;21(7):827. PMID: 24275586)
Olanow CW, Watts RL, Koller WC (2001) An algorithm (decision tree) for the management of Parkinson’s disease (2001): treatment guidelines. Neurology 56(11 Suppl 5):S1–S88. https://doi.org/10.1212/wnl.56.suppl_5.s1 (PMID: 11402154)
Brotchie JM (2000) The neural mechanisms underlying levodopa-induced dyskinesia in Parkinson’s disease. Ann Neurol 47(4 Suppl 1):S105–S112 (discussion S112–4. PMID: 1076213)
Obeso JA, Rodriguez-Oroz MC, Chana P, Lera G, Rodriguez M, Olanow CW (2000) The evolution and origin of motor complications in Parkinson’s disease. Neurology 55(11 Suppl 4):S13–S20 (discussion S21–3. PMID: 11147505)
Calon F, Rajput AH, Hornykiewicz O, Bédard PJ, Di Paolo T (2003) Levodopa-induced motor complications are associated with alterations of glutamate receptors in Parkinson’s disease. Neurobiol Dis 14(3):404–416. https://doi.org/10.1016/j.nbd.2003.07.003 (PMID: 14678757)
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The authors thank the investigators and the patients involved in the trial. Zambon S.p.A funded the study.
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The Belgian Safinamide Study Group., Bergmans, B., Bourgeois, P. et al. Effectiveness and safety of safinamide in routine clinical practice in a Belgian Parkinson’s disease population: an open-label, levodopa add-on study. Acta Neurol Belg 123, 939–947 (2023). https://doi.org/10.1007/s13760-022-02100-1
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DOI: https://doi.org/10.1007/s13760-022-02100-1