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1.
Rev Neurol ; 55(11): 669-88, 2012 Dec 01.
Artigo em Espanhol | MEDLINE | ID: mdl-23172094

RESUMO

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.


Assuntos
Antiparkinsonianos/uso terapêutico , Levodopa/uso terapêutico , Doença de Parkinson/tratamento farmacológico , Antiparkinsonianos/farmacologia , Humanos , Levodopa/farmacologia , Transtornos Mentais/etiologia , Atividade Motora/efeitos dos fármacos , Doença de Parkinson/complicações , Doença de Parkinson/fisiopatologia , Qualidade de Vida , Transtornos do Sono-Vigília/etiologia
3.
Neurosci Lett ; 467(3): 208-11, 2009 Dec 31.
Artigo em Inglês | MEDLINE | ID: mdl-19835934

RESUMO

Progressive supranuclear palsy (PSP) and multiple system atrophy (MSA) are both rare neurodegenerative diseases. In the Queen Square Brain Bank, from 2001 to 2008, we received 120 cases of pathologically confirmed PSP and 36 of MSA, and one had concomitant PSP and MSA pathology. The clinical symptoms in this case were compatible with PSP and did not predict the dual pathology. The growing number of collective case reports, including the one reported here, might suggest an increased prevalence of concomitant PSP and MSA than what would be expected by chance.


Assuntos
Encéfalo/patologia , Atrofia de Múltiplos Sistemas/epidemiologia , Atrofia de Múltiplos Sistemas/patologia , Neurônios/patologia , Paralisia Supranuclear Progressiva/epidemiologia , Paralisia Supranuclear Progressiva/patologia , Idoso , Astrócitos/metabolismo , Astrócitos/patologia , Biomarcadores/metabolismo , Encéfalo/metabolismo , Encéfalo/fisiopatologia , Comorbidade , Progressão da Doença , Feminino , Humanos , Imuno-Histoquímica , Corpos de Inclusão/metabolismo , Corpos de Inclusão/patologia , Programas de Rastreamento , Atrofia de Múltiplos Sistemas/fisiopatologia , Vias Neurais/metabolismo , Vias Neurais/patologia , Neurônios/metabolismo , Oligodendroglia/metabolismo , Oligodendroglia/patologia , Doença de Parkinson/epidemiologia , Doença de Parkinson/patologia , Doença de Parkinson/fisiopatologia , Prevalência , Índice de Gravidade de Doença , Paralisia Supranuclear Progressiva/fisiopatologia , alfa-Sinucleína/metabolismo , Proteínas tau/metabolismo
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