Tachikawa H, Harada S, Kawanishi Y, Okubo T, Shiraishi H
Department of Psychiatry, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan.
Am J Med Genet. 1999 Dec 15;88(6):700-4.
Genetic variations in the 5'-untranslated region and the coding region of the CCK-B receptor (CCK-BR) gene were investigated in healthy controls. Novel variants (-215 C-->A, Leu37Phe, Arg319Glu) were found in addition to the mutations (Val125Iso, His207His, Arg215His, 2491 C-->A) reported previously. In the present study, association analysis was carried out for these variants between 80 unrelated schizophrenic patients and 100 healthy controls. The genotype frequency of the -215 C-->A nucleotide substitution in the 5'-untranslated region of CCK-BR gene was significantly higher in the schizophrenic patients than in the controls (6.25%, P = 0.037). However, the difference was not significant after Bonferroni correction for multiple comparisons. Moreover, no association was found between the clinical characteristics of the patients and the genotype frequencies of the variants. These results suggest that the CCK-BR gene polymorphisms have no association with schizophrenia nor its clinical heterogeneity. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 88:700-704, 1999.
在健康对照人群中研究了CCK - B受体(CCK - BR)基因5'-非翻译区和编码区的遗传变异。除了先前报道的突变(Val125Iso、His207His、Arg215His、2491 C→A)外,还发现了新的变异(-215 C→A、Leu37Phe、Arg319Glu)。在本研究中,对80名无亲缘关系的精神分裂症患者和100名健康对照人群的这些变异进行了关联分析。CCK - BR基因5'-非翻译区-215 C→A核苷酸替换的基因型频率在精神分裂症患者中显著高于对照人群(6.25%,P = 0.037)。然而,在进行多重比较的Bonferroni校正后,差异不显著。此外,未发现患者的临床特征与变异的基因型频率之间存在关联。这些结果表明,CCK - BR基因多态性与精神分裂症及其临床异质性均无关联。《美国医学遗传学杂志》(神经精神遗传学)88:700 - 704,1999年。