Role of LINGO1 polymorphisms in Parkinson's disease
Identifieur interne : 000E92 ( Istex/Curation ); précédent : 000E91; suivant : 000E93Role of LINGO1 polymorphisms in Parkinson's disease
Auteurs : Dietrich Haubenberger [Autriche] ; Christoph Hotzy [Autriche] ; Walter Pirker [Autriche] ; Regina Katzenschlager [Autriche] ; Thomas Brücke [Autriche] ; Fritz Zimprich [Autriche] ; Eduard Auff [Autriche] ; Alexander Zimprich [Autriche]Source :
- Movement Disorders [ 0885-3185 ] ; 2009-12-15.
English descriptors
Abstract
A clinical overlap between Parkinson's disease (PD) and essential tremor (ET) has prompted a discussion whether these conditions share common genetic susceptibility factors. Recently, the first genome‐wide association study in ET revealed a significant association with a variant in the LINGO1 gene. LINGO1 has also been demonstrated to play a role in the survival of dopaminergic neurons in an animal model of PD, and therefore constitutes a potential candidate gene for PD. In this study, SNPs rs9652490, rs11856808, and rs7177008 of LINGO1 were genotyped in a total of 694 Austrian subjects (349 PD, 345 controls). No association could be found between genotype or allele counts and PD. Neither did a subgroup analysis in tremor‐dominant patients with PD reveal a significant association. This study on LINGO1‐variants in PD argues against a major role of LINGO1 gene variations for PD. © 2009 Movement Disorder Society
Url:
DOI: 10.1002/mds.22768
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<front><div type="abstract" xml:lang="fr">A clinical overlap between Parkinson's disease (PD) and essential tremor (ET) has prompted a discussion whether these conditions share common genetic susceptibility factors. Recently, the first genome‐wide association study in ET revealed a significant association with a variant in the LINGO1 gene. LINGO1 has also been demonstrated to play a role in the survival of dopaminergic neurons in an animal model of PD, and therefore constitutes a potential candidate gene for PD. In this study, SNPs rs9652490, rs11856808, and rs7177008 of LINGO1 were genotyped in a total of 694 Austrian subjects (349 PD, 345 controls). No association could be found between genotype or allele counts and PD. Neither did a subgroup analysis in tremor‐dominant patients with PD reveal a significant association. This study on LINGO1‐variants in PD argues against a major role of LINGO1 gene variations for PD. © 2009 Movement Disorder Society</div>
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