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1.
Brain Sci ; 9(10)2019 Oct 11.
Artículo en Inglés | MEDLINE | ID: mdl-31614574

RESUMEN

Background: Safinamide is an approved drug for the treatment of motor fluctuations of Parkinson's Disease (PD) patients with a potential benefit on non-motor symptoms (NMS). Methods: A retrospective multicenter cohort study was conducted, in which the clinical effect of safinamide on both motor and NMS was assessed by the Clinical Global Impression of Change scale. Furthermore, we assessed the appearance of adverse events (AEs) and its effect on dyskinesia, that were also recorded in non-fluctuating PD patients and in those previously treated with rasagiline. Results: We included 213 PD patients who received safinamide in addition to their regular levodopa therapy. Thirty-five withdrew prematurely from safinamide, mainly because of AEs. Out of 178, clinical improvement on motor and NMS was found in 76.4% and 26.2%, respectively. A total of 44 reported AEs of mild intensity. We did not find a difference concerning the clinical benefit or AEs when comparing either patients who had or had not been taking Monoamine Oxidase B Inhibitor (MAOB-I) previously or between patients with and without motor complications. Conclusions: Safinamide is an effective and safe add-on to levodopa drug for PD patients. Moreover, safinamide could elicit an additional clinical improvement in PD patients previously treated with other MAOB-I and in non- fluctuating patients with suboptimal motor control.

3.
Rev. neurol. (Ed. impr.) ; 55(11): 669-688, 1 dic., 2012.
Artículo en Español | IBECS | ID: ibc-109576

RESUMEN

Durante los últimos años hemos sido testigos de una utilización preferente de agonistas dopaminérgicos (AD) como tratamiento de la enfermedad de Parkinson (EP), con la intención de retrasar en lo posible el desarrollo de fluctuaciones y discinesias. Sin embargo, la levodopa continúa siendo el fármaco antiparkinsoniano más eficaz y, probablemente, el que mejora un mayor número de síntomas de la enfermedad. En este artículo se ha realizado una revisión exhaustiva de la literatura por parte de un grupo de neurólogos expertos y miembros del Grupo de Trastornos del Movimiento de la Sociedad Española de Neurología sobre los beneficios y riesgos del tratamiento con levodopa en pacientes con EP. La principal conclusión de este artículo es que la levodopa continúa siendo el tratamiento más eficaz para la EP. Aunque el riesgo y la incidencia de desarrollar discinesias se mantiene en un nivel menor en el grupo tratado inicialmente con AD, el número de pacientes que desarrollan discinesias incapacitantes es muy bajo en todos los estudios y similar para los AD y la levodopa, y las escalas de calidad de vida son también similares en ambos grupos, lo que cuestiona el impacto que estas complicaciones motoras tienen sobre la calidad de vida de los pacientes con EP. A la vista de estos resultados, deberíamos plantearnos si está justificado privar a los pacientes del buen control de los síntomas que proporciona la levodopa por el temor a que desarrollen discinesias o fluctuaciones motoras leves que no van a mermar su calidad de vida. A ello hay que añadir la posibilidad de que desarrollen efectos secundarios graves, que son más frecuentes con el uso de AD (AU)


In recent years we have witnessed a growing tendency to opt for the use of dopamine agonists (DA) as treatment for Parkinson’s disease (PD), with the aim of delaying as far as possible the development of fluctuations and dyskinesias. Yet, levodopa continues to be the most effective antiparkinson drug and is probably the one that improves the greatest number of symptoms of the disease. This article reports on the results of a comprehensive review of the literature dealing with the benefits and risks of levodopa treatment in patients with PD which was conducted by a group of expert neurologists and members of the Spanish Neurology Society’s Movement Disorder Group. The main conclusion reached in this article is that levodopa continues to be the most effective treatment for PD. Although the risk and incidence of developing dyskinesias remains at a lower level in the group initially treated with DA, the number of patients who develop disabling dyskinesias is very low in all the studies and is similar for DA and for levodopa. Scores on the quality of life scales are also similar in the two groups, which casts some doubt on the impact that these motor complications have on the quality of life of patients with PD. In view of these findings, we should consider whether there is any real justification for depriving patients of the good control of their symptoms offered by levodopa owing to the fear of developing dyskinesias or mild motor fluctuations that are not really going to have any negative effect on their quality of life. There is also the possibility of their developing severe side effects, which are more frequent with the use of DA (AU)


Asunto(s)
Humanos , Enfermedad de Parkinson/tratamiento farmacológico , Levodopa/uso terapéutico , /métodos , Calidad de Vida , Discinesias/tratamiento farmacológico , Agonistas de Dopamina/uso terapéutico , Factores de Riesgo
4.
Rev Neurol ; 55(11): 669-88, 2012 Dec 01.
Artículo en Español | MEDLINE | ID: mdl-23172094

RESUMEN

In recent years we have witnessed a growing tendency to opt for the use of dopamine agonists (DA) as treatment for Parkinson's disease (PD), with the aim of delaying as far as possible the development of fluctuations and dyskinesias. Yet, levodopa continues to be the most effective antiparkinson drug and is probably the one that improves the greatest number of symptoms of the disease. This article reports on the results of a comprehensive review of the literature dealing with the benefits and risks of levodopa treatment in patients with PD which was conducted by a group of expert neurologists and members of the Spanish Neurology Society's Movement Disorder Group. The main conclusion reached in this article is that levodopa continues to be the most effective treatment for PD. Although the risk and incidence of developing dyskinesias remains at a lower level in the group initially treated with DA, the number of patients who develop disabling dyskinesias is very low in all the studies and is similar for DA and for levodopa. Scores on the quality of life scales are also similar in the two groups, which casts some doubt on the impact that these motor complications have on the quality of life of patients with PD. In view of these findings, we should consider whether there is any real justification for depriving patients of the good control of their symptoms offered by levodopa owing to the fear of developing dyskinesias or mild motor fluctuations that are not really going to have any negative effect on their quality of life. There is also the possibility of their developing severe side effects, which are more frequent with the use of DA.


Asunto(s)
Antiparkinsonianos/uso terapéutico , Levodopa/uso terapéutico , Enfermedad de Parkinson/tratamiento farmacológico , Antiparkinsonianos/farmacología , Humanos , Levodopa/farmacología , Trastornos Mentales/etiología , Actividad Motora/efectos de los fármacos , Enfermedad de Parkinson/complicaciones , Enfermedad de Parkinson/fisiopatología , Calidad de Vida , Trastornos del Sueño-Vigilia/etiología
5.
Rev Neurol ; 50(10): 591-4, 2010 May 16.
Artículo en Español | MEDLINE | ID: mdl-20473834

RESUMEN

INTRODUCTION: LRRK2 mutations have been described as a common cause of Parkinson's disease (PD) in patients from northern Spain. Here we investigated the prevalence of these mutations in a cohort of Spanish PD patients (n = 96) from Extremadura, a region in southwestern Spain. SUBJECTS AND METHODS: To evaluate the rate of the G2019S and R1441G/C/H LRKK2 mutations in PD patients and healthy controls (n = 163). RESULTS: Here we show that the G2019S mutation is present at a low prevalence in our Spanish cohort, while the R1441G/C/H mutation, which has been reported to be common in northern Spain, was not observed in the PD patients or in the controls. CONCLUSION: LRRK2 mutations do not appear to be a common cause of Parkinson's disease in Extremadura, Spain.


Asunto(s)
Codón , Mutación , Enfermedad de Parkinson/genética , Proteínas Serina-Treonina Quinasas/genética , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Marcadores Genéticos , Predisposición Genética a la Enfermedad , Pruebas Genéticas , Humanos , Proteína 2 Quinasa Serina-Treonina Rica en Repeticiones de Leucina , Masculino , Persona de Mediana Edad , Linaje , España
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