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Article: Monoamine oxidase-B (MAO-B) inhibitors: Implications for disease-modification in Parkinson's disease

TitleMonoamine oxidase-B (MAO-B) inhibitors: Implications for disease-modification in Parkinson's disease
Authors
KeywordsDisease-modification
Monoamine oxidase-B inhibitors
Neuroprotection
Parkinson's disease
Rasagiline
Selegiline
Issue Date2013
Citation
Translational Neurodegeneration, 2013, v. 2, n. 1, article no. 19 How to Cite?
AbstractThere is a substantial amount of evidence from experimental parkinsonian models to show the neuroprotective effects of monoamine oxidase-B (MAOB) inhibitors. They have been studied for their potential disease-modifying effects in Parkinson's disease (PD) for over 20 years in various clinical trials. This review provides a summary of the clinical trials and discusses the implications of their results in the context of disease-modification in PD. Earlier clinical trials on selegiline were confounded by symptomatic effects of this drug. Later clinical trials on rasagiline using delayed-start design provide newer insights in disease-modification in PD but success in achieving the aims of this strategy remain elusive due to obstacles, some of which may be insurmountable. © 2013 Teo and Ho; licensee BioMed Central Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/336119
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTeo, Kay Cheong-
dc.contributor.authorHo, Shu Leong-
dc.date.accessioned2024-01-15T08:23:38Z-
dc.date.available2024-01-15T08:23:38Z-
dc.date.issued2013-
dc.identifier.citationTranslational Neurodegeneration, 2013, v. 2, n. 1, article no. 19-
dc.identifier.urihttp://hdl.handle.net/10722/336119-
dc.description.abstractThere is a substantial amount of evidence from experimental parkinsonian models to show the neuroprotective effects of monoamine oxidase-B (MAOB) inhibitors. They have been studied for their potential disease-modifying effects in Parkinson's disease (PD) for over 20 years in various clinical trials. This review provides a summary of the clinical trials and discusses the implications of their results in the context of disease-modification in PD. Earlier clinical trials on selegiline were confounded by symptomatic effects of this drug. Later clinical trials on rasagiline using delayed-start design provide newer insights in disease-modification in PD but success in achieving the aims of this strategy remain elusive due to obstacles, some of which may be insurmountable. © 2013 Teo and Ho; licensee BioMed Central Ltd.-
dc.languageeng-
dc.relation.ispartofTranslational Neurodegeneration-
dc.subjectDisease-modification-
dc.subjectMonoamine oxidase-B inhibitors-
dc.subjectNeuroprotection-
dc.subjectParkinson's disease-
dc.subjectRasagiline-
dc.subjectSelegiline-
dc.titleMonoamine oxidase-B (MAO-B) inhibitors: Implications for disease-modification in Parkinson's disease-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1186/2047-9158-2-19-
dc.identifier.scopuseid_2-s2.0-84884190046-
dc.identifier.volume2-
dc.identifier.issue1-
dc.identifier.spagearticle no. 19-
dc.identifier.epagearticle no. 19-
dc.identifier.eissn2047-9158-
dc.identifier.isiWOS:000215872400018-

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