Maeno Nobuhisa, Takahashi Nagahide, Saito Shinichi, Ji Xiaofei, Branko Aleksic, Ishihara Ryoko, Yoshida Keizo, Inada Toshiya, Iidaka Tetsuya, Ozaki Norio
Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Neuroreport. 2007 Mar 26;18(5):517-20. doi: 10.1097/WNR.0b013e3280586890.
Several lines of evidence, including diffusion tensor imaging and microarray studies, indicate that abnormalities in myelination play an important role in the pathophysiology of schizophrenia. Of myelin and oligodendrocyte-related genes, a significant decrease in the mRNA levels of transferrin in schizophrenics has been reported by both microarray and quantitative polymerase chain reaction studies. We performed an association analysis of the transferrin gene in a Japanese population of 384 schizophrenic patients and 384 controls. Six single nucleotide polymorphisms were genotyped by polymerase chain reaction-restriction fragment length polymorphism and a TaqMan assay. No significant differences in genotype, allele, or haplotype frequencies of the six single nucleotide polymorphisms were observed between schizophrenic patients and controls. The present results suggest that the transferrin gene is not related to the development of schizophrenia in the Japanese population.
包括扩散张量成像和微阵列研究在内的多项证据表明,髓鞘形成异常在精神分裂症的病理生理学中起重要作用。在与髓鞘和少突胶质细胞相关的基因中,微阵列和定量聚合酶链反应研究均报告称,精神分裂症患者转铁蛋白的mRNA水平显著降低。我们对384例日本精神分裂症患者和384例对照人群进行了转铁蛋白基因关联分析。通过聚合酶链反应-限制性片段长度多态性和TaqMan检测对6个单核苷酸多态性进行基因分型。在精神分裂症患者和对照之间,未观察到这6个单核苷酸多态性的基因型、等位基因或单倍型频率有显著差异。目前的结果表明,在日本人群中,转铁蛋白基因与精神分裂症的发生无关。