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Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2.
Estanga, A; Rodriguez-Oroz, M C; Ruiz-Martinez, J; Barandiaran, M; Gorostidi, A; Bergareche, A; Mondragon, E; Lopez de Munain, A; Marti-Masso, J F.
Afiliación
  • Estanga A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neuroscience, University of the Basque Country UPV/EHU, Spain. Electronic address: ainara.estangaalustiza@osakidetza.net.
  • Rodriguez-Oroz MC; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain; Ikerbasque, Basque Foundation for Science, Bilbao, Spain.
  • Ruiz-Martinez J; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Barandiaran M; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Gorostidi A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain.
  • Bergareche A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Mondragon E; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Lopez de Munain A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain; Department of Neuroscience, University of the Basque Country UPV/EHU, Spain.
  • Marti-Masso JF; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain; Department of Neuroscience, University of the Basque Country UPV/EHU, Spain.
Parkinsonism Relat Disord ; 20(10): 1097-100, 2014 Oct.
Article en En | MEDLINE | ID: mdl-25127457
ABSTRACT

OBJECTIVE:

The neuropsychological characteristics of patients with Parkinson's Disease (PD) associated with R1441G mutation in the LRRK2 gene (R1441G-PD) are not well known. The aim of this study was to examine the cognitive status and mood of R1441G-PD patients.

METHODS:

Thirty patients with R1441G-PD were compared with thirty idiopathic PD (i-PD) patients who were matched by age, sex, education, disease onset age and duration, using a comprehensive battery of neuropsychological test, and considering the Movement Disorder Society (MDS) criteria for the diagnosis of Mild Cognitive Impairment (PD-MCI) and dementia (PD-Dementia).

RESULTS:

The mean scores in the depression and anxiety scales were similar in the two groups. Depressive symptoms were detected in 31.8% of R1441G-PD and 25% of i-PD patients and anxiety symptoms were evident in 4.5% and 15%, respectively, but the differences were not significant. The only neuropsychological test on which there was a significantly worse performance in the R1441G-PD group was the Boston naming test but the difference became not significant when Bonferroni's correction was applied. The prevalence of PD-MCI was 30% in both R1441G-PD and i-PD, with no differences in the number and type of domains altered given that executive function, memory and attention were mainly affected. PD-Dementia was diagnosed in 13.3% (n = 4) of R1441G-PD and 26.7% (n = 8) of i-PD patients (difference was not significant).

CONCLUSION:

In conclusion, significant differences were not detected between R1441G-PD and i-PD in cognitive, depression and anxiety scales, or PD-MCI and PD-Dementia prevalence, and the cognitive profile was identical in the two groups.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas Serina-Treonina Quinasas / Trastornos del Conocimiento / Mutación Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas Serina-Treonina Quinasas / Trastornos del Conocimiento / Mutación Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2014 Tipo del documento: Article
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