FMR1 alleles in Parkinson's disease: relation to cognitive decline and hallucinations, a longitudinal study
Autor: | Thomas Mueller, Yvonne Klenk, Jan Petter Larsen, Gabriele Dekomien, Dag Aarsland, Anna Melissa Schlitter, Martin Wilhelm Kurz |
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Rok vydání: | 2007 |
Předmět: |
0301 basic medicine
Adult Male congenital hereditary and neonatal diseases and abnormalities medicine.medical_specialty Parkinson's disease Hallucinations DNA Mutational Analysis Statistics as Topic Neuropsychological Tests 03 medical and health sciences Fragile X Mental Retardation Protein 0302 clinical medicine Degenerative disease Trinucleotide Repeats Internal medicine medicine Dementia Humans Longitudinal Studies Cognitive decline Psychiatry Alleles Aged Neurologic Examination Parkinsonism Genetic Carrier Screening Cognitive disorder Parkinson Disease Middle Aged medicine.disease FMR1 nervous system diseases Fragile X syndrome Psychiatry and Mental health 030104 developmental biology Endocrinology 030220 oncology & carcinogenesis Neurology (clinical) Geriatrics and Gerontology Psychology Cognition Disorders Mental Status Schedule |
Zdroj: | Journal of geriatric psychiatry and neurology. 20(2) |
ISSN: | 0891-9887 |
Popis: | Carriers of expanded alleles of the fragile X mental retardation ( FMR1) gene may display parkinsonism, cognitive decline, and behavioral changes. The authors screened 2 male groups of patients affected with Parkinson's disease (PD) (n = 137). One group (n = 56) was followed longitudinally for up to 12 years. Length of CGG repeats in PD patients was compared with healthy controls (n = 310). In addition, the association of the number of CGG repeats with cognitive decline or hallucinations was studied in the longitudinally followed PD group. The authors found no repeats in the premutation range (55-200 CGG repeats) and no significant difference in the proportion of intermediate-size (41-54 CGG repeats) carriers between the PD and the control groups. Using linear regression, the number of CGG repeats was not related to motor or cognitive progression. However, the marked cognitive decline in 2 patients carrying intermediate-size alleles points to a possible association. More studies with larger PD samples are warranted. ( J Geriatr Psychiatry Neurol 2007;20:89-92) |
Databáze: | OpenAIRE |
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