Eye movements in ephedrone-induced parkinsonism
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25117825
PubMed Central
PMC4130591
DOI
10.1371/journal.pone.0104784
PII: PONE-D-14-11282
Knihovny.cz E-zdroje
- MeSH
- bazální ganglia patofyziologie MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mangan toxicita MeSH
- mozek patofyziologie MeSH
- parkinsonské poruchy chemicky indukované patofyziologie MeSH
- pohyby očí fyziologie MeSH
- poruchy spojené s užíváním psychoaktivních látek patofyziologie MeSH
- propiofenony škodlivé účinky MeSH
- sakadické oční pohyby fyziologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- mangan MeSH
- monomethylpropion MeSH Prohlížeč
- propiofenony MeSH
Patients with ephedrone parkinsonism (EP) show a complex, rapidly progressive, irreversible, and levodopa non-responsive parkinsonian and dystonic syndrome due to manganese intoxication. Eye movements may help to differentiate parkinsonian syndromes providing insights into which brain networks are affected in the underlying disease, but they have never been systematically studied in EP. Horizontal and vertical eye movements were recorded in 28 EP and compared to 21 Parkinson's disease (PD) patients, and 27 age- and gender-matched healthy subjects using standardized oculomotor tasks with infrared videooculography. EP patients showed slow and hypometric horizontal saccades, an increased occurrence of square wave jerks, long latencies of vertical antisaccades, a high error rate in the horizontal antisaccade task, and made more errors than controls when pro- and antisaccades were mixed. Based on oculomotor performance, a direct differentiation between EP and PD was possible only by the velocity of horizontal saccades. All remaining metrics were similar between both patient groups. EP patients present extensive oculomotor disturbances probably due to manganese-induced damage to the basal ganglia, reflecting their role in oculomotor system.
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