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Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease.
Shanker, Vicki; Groves, Mark; Heiman, Gary; Palmese, Christina; Saunders-Pullman, Rachel; Ozelius, Laurie; Raymond, Deborah; Bressman, Susan.
Afiliação
  • Shanker V; Beth Israel Medical Center, 10 Union Square East, Suite 5H, New York, NY 10003, USA. vshanker@chpnet.org
Mov Disord ; 26(10): 1875-80, 2011 Aug 15.
Article em En | MEDLINE | ID: mdl-21611978
ABSTRACT
The behavioral and cognitive features of the leucine-rich repeat kinase G2019S mutation in Parkinson's disease in the Ashkenazi Jewish population are not well described; therefore, we sought to more systematically characterize these features using a semistructured psychiatric interview and neuropsychological testing. Twenty-one Ashkenazi Jewish patients having the leucine-rich repeat kinase G2019S mutation were compared with age- and sex-matched Ashkenazi Jewish patients with Parkinson's disease without mutations. Although overall rates of affective disorders were not greater in mutation carriers, the carriers exhibited a 6-fold increased risk of premorbid affective disorders (odds ratio, 6.0; P = .10), as determined by the Structured Clinical Interview for the Diagnostic and Statistical Manual of Mental Disorders-IV. Of interest, we identified 2 leucine-rich repeat kinase carriers with bipolar disorder; no mutation-negative subjects had this diagnosis. Performance on the Hopkins Verbal Learning Test-Revised, Judgment of Line Orientation, and Frontal Assessment Battery was consistent with previous reports and did not differ between groups. Study findings suggest a possible association between premorbid mood disorders and leucine-rich repeat kinase Parkinson's disease, warranting further evaluation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Serina / Proteínas Serina-Treonina Quinases / Transtornos Cognitivos / Transtornos do Humor / Predisposição Genética para Doença / Glicina Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Serina / Proteínas Serina-Treonina Quinases / Transtornos Cognitivos / Transtornos do Humor / Predisposição Genética para Doença / Glicina Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Estados Unidos