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Prog Neuropsychopharmacol Biol Psychiatry ; 37(1): 62-75, 2012 Apr 27.
Artigo em Inglês | MEDLINE | ID: mdl-22203087

RESUMO

OBJECTIVES: This study aimed to: 1) replicate previously reported associations between dopamine D4 receptor gene (DRD4) polymorphisms and antipsychotic (AP) response in a clozapine (CLZ) response sample; and 2) explore possible associations of polymorphisms across dopamine D5 receptor gene (DRD5) as well as other DRD4 regions. METHODS: DRD4 exon III 48-bp, intron I (G)(n), and 120-bp repeat polymorphisms, and three DRD4 single nucleotide polymorphisms (SNPs); and DRD5 (CA/CT/GT)(n) microsatellite and four DRD5 SNPs were assessed using standard genotyping and statistical procedures. RESULTS: We report evidence, which does not survive correction for multiple testing, supporting previous DRD4 findings. Findings of interest include the 120-bp 1-copy allele, intron I (G)(n) 142-bp/140-bp genotype, and exon III 4R allele with CLZ response. All DRD5 tests were negative. CONCLUSIONS: Overall, these results suggest a possible minor contribution of DRD4 variants, but not DRD5 variants, towards the AP/CLZ response phenotype.


Assuntos
Clozapina/uso terapêutico , Variação Genética/genética , Receptores de Dopamina D4/genética , Receptores de Dopamina D5/genética , Esquizofrenia/tratamento farmacológico , Esquizofrenia/genética , Antipsicóticos/uso terapêutico , População Negra/genética , Feminino , Humanos , Masculino , Polimorfismo de Nucleotídeo Único/genética , Estudos Prospectivos , Esquizofrenia/etnologia , Resultado do Tratamento , População Branca/genética
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