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1.
Biol Psychiatry ; 54(2): 129-35, 2003 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-12873802

RESUMO

BACKGROUND: A family based association study in a British sample found the NOTCH4 gene to be associated with schizophrenia; however, all six replication studies failed to confirm the finding. METHODS: We performed a family based association study of NOTCH4 and schizophrenia in 123 trios (16 Japanese and 107 Chinese). In addition to the original study's polymorphisms, we examined four new single nucleotide polymorphisms (SNPs)--SNPs_A, B, C and D--around SNP1 of the original study. We genotyped all samples for SNPs_A-D and for SNP1 and (CTG)n of the original study. RESULTS: We found no significant associations between NOTCH4 and schizophrenia or its subtypes for all polymorphisms, regardless of gender. The finding remained negative when the Chinese sample was analyzed separately. Exploratory analyses suggested that SNP_A may be associated with early-onset schizophrenia and that SNP1 may be associated with schizophrenia characterized by numerous negative symptoms. CONCLUSIONS: NOTCH4 is not a significant susceptibility gene for schizophrenia when clinical heterogeneity is ignored; however, NOTCH4 may be associated with early-onset schizophrenia or schizophrenia with many negative symptoms, but these findings should be interpreted cautiously.


Assuntos
Povo Asiático/genética , Polimorfismo Genético , Proteínas Proto-Oncogênicas/genética , Receptores de Superfície Celular , Esquizofrenia/genética , Adulto , Idade de Início , Idoso , China , Família , Feminino , Genótipo , Haplótipos , Humanos , Japão , Masculino , Pessoa de Meia-Idade , Receptor Notch4 , Receptores Notch
2.
Am J Med Genet B Neuropsychiatr Genet ; 120B(1): 11-7, 2003 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-12815732

RESUMO

Several studies suggest that loci at chromosome 22q11.2-q13 might be linked to susceptibility to schizophrenia. Here we performed family-based association studies on chromosome 22q using 12 DNA microsatellite markers in African-American, European-American, and Chinese pedigrees. The marker D22S683 showed significant linkage and association with schizophrenia in not only the European-American sample but also in a combined sample (European-American and Chinese samples). Notably, D22S683 is located nearby and between D22S278 and D22S283, which have shown linkage and association to schizophrenia in prior reports. However, we found no significant association for the African-American sample. In conclusion, our data provide further support for the idea that the region around D22S683 contains a susceptibility gene for schizophrenia.


Assuntos
Povo Asiático/genética , População Negra/genética , Cromossomos Humanos Par 22/genética , Esquizofrenia/genética , População Branca/genética , Adulto , População Negra/etnologia , Mapeamento Cromossômico , Feminino , Ligação Genética , Marcadores Genéticos , Genótipo , Humanos , Masculino , Repetições de Microssatélites , Pessoa de Meia-Idade , Núcleo Familiar , Linhagem , População Branca/etnologia
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