Association of serotonin transporter linked polymorphic region 44 bp variable number of tandem repeat polymorphism with Tourette syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 646-649, 2014.
Artigo
em Chinês
| WPRIM
| ID: wpr-291710
ABSTRACT
<p><b>OBJECTIVE</b>To assess the association between the serotonin transporter linked polymorphic region (5-HTTLPR) 44 bp variable number of tandem repeat (VNTR) polymorphism and Tourette syndrome (TS) in ethnic Han Chinese trios.</p><p><b>METHODS</b>A total of 252 TS trios (patients and their parents) were recruited. Genetic contribution of the 5-HTTLPR 44 bp VNTR polymorphism was evaluated by genotyping, haplotype relative risk (HRR) analysis and transmission disequilibrium test (TDT) statistics. To enhance the efficiency of the test, haplotype-based HRR (HHRR) was also performed.</p><p><b>RESULTS</b>The TDT, HRR and HHRR analyses have revealed a significant association of the 5-HTTLPR 44 bp VNTR polymorphism with TS, and provided a strong evidence for an over-transmission of L allele from parents to the affected children (TDT χ² = 6.680, df= 1, P= 0.012; HRR χ² = 9.345, P= 0.002, OR= 1.739, 95% CI for 1.218-2.483). For 204 male and 48 female TS trios, TDT and HRR were analyzed separately. The results showed a significant association between 5-HTTLPR and male TS (for males. TDT χ² = 4.643, df= 1, P= 0.038; for females, TDT χ² = 2.189, df= 1, P= 0.188).</p><p><b>CONCLUSION</b>5-HTTLPR may be the susceptibility gene for male TS patients among the Chinese Han population. However, the results need to be replicated in datasets collected from different populations.</p>
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Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Polimorfismo Genético
/
Síndrome de Tourette
/
Desequilíbrio de Ligação
/
China
/
Fatores Sexuais
/
Repetições Minissatélites
/
Predisposição Genética para Doença
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Povo Asiático
/
Proteínas da Membrana Plasmática de Transporte de Serotonina
/
Frequência do Gene
Tipo de estudo:
Estudo de etiologia
Limite:
Adolescente
/
Criança
/
Criança, pré-escolar
/
Feminino
/
Humanos
/
Masculino
País/Região como assunto:
Ásia
Idioma:
Chinês
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2014
Tipo de documento:
Artigo
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