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Association between Antipsychotic-Related Restless Legs Syndrome and the RORA Gene Polymorphism in Schizophrenia / 대한정신분열병학회지
Korean Journal of Schizophrenia Research ; : 93-97, 2013.
Article Dans Coréen | WPRIM | ID: wpr-67158
ABSTRACT

OBJECTIVES:

The previous studies have suggested genetic vulnerability to restless legs syndrome (RLS) development. The occurrence of antipsychotic-related RLS could also be attributable to differences in genetic susceptibility. This study aimed to investigate whether Retinoid-related orphan receptor A (RORA) gene polymorphism is associated with antipsychotic-related RLS in schizophrenia.

METHODS:

We assessed symptoms of antipsychotic-induced RLS in 190 Korean schizophrenic patients and divided the subjects into two groups according to the International Restless Legs Syndrome Study Group diagnostic criteria 1) subjects that met all of the criteria (n=44) and 2) the remaining subjects who were not considered to be RLS patients (n=146). Single-nucleotide polymorphism in the RORA gene was genotyped by PCR in 190 individuals. The chi2-test was conducted to compare differences between two groups.

RESULTS:

The frequencies of genotype (chi2=0.066, p=0.968) of the RORA gene (rs11071547) did not differ significantly between schizophrenic patients with and without RLS. The difference of allele frequencies (chi2=0.008, p=0.927) of the RORA gene (rs 11071547) between the schizophrenic patients with and without RLS were not significant.

CONCLUSION:

These results suggest that RORA gene polymorphism does not play a major role in susceptibility to antipsychotic-related RLS in schizophrenia.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Polymorphisme génétique / Syndrome des jambes sans repos / Schizophrénie / Réaction de polymérisation en chaîne / Rythme circadien / Prédisposition génétique à une maladie / Enfant orphelin / Fréquence d'allèle / Génotype Limites du sujet: Enfant / Humains langue: Coréen Texte intégral: Korean Journal of Schizophrenia Research Année: 2013 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Polymorphisme génétique / Syndrome des jambes sans repos / Schizophrénie / Réaction de polymérisation en chaîne / Rythme circadien / Prédisposition génétique à une maladie / Enfant orphelin / Fréquence d'allèle / Génotype Limites du sujet: Enfant / Humains langue: Coréen Texte intégral: Korean Journal of Schizophrenia Research Année: 2013 Type: Article