Inoue Yoshiaki, Shinkai Takahiro, Utsunomiya Kensuke, Sakata Shinichi, Fukunaka Yuko, Yamaguchi Wakana, Yamada Kenji, Chen Hsin-I, Hwang Rudi, Ohmori Osamu, Nakamura Jun
Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.
Neurosci Lett. 2009 Mar 6;452(1):72-4. doi: 10.1016/j.neulet.2009.01.005. Epub 2009 Jan 8.
It has been suggested that hypoactivity of neuropeptide Y (NPY) may be involved in the pathophysiology of schizophrenia. A post-mortem study revealed a decreased level of NPY in the brain of patients with schizophrenia. An increased level of NPY after antipsychotic treatment was also reported in animal brain and cerebrospinal fluid of patients. Previously Itokawa et al. reported a positive association between the functional -485C>T polymorphism in the NPY gene and schizophrenia in a Japanese population. The aim of this study is to replicate their positive findings in an independent Japanese case-control sample. Our sample includes 260 patients with schizophrenia (DSM-IV) and 196 control subjects. No significant differences in distribution of genotype or allele frequencies between patients and controls were observed. Our results suggest that the NPY -485C>T polymorphism may not confer susceptibility to schizophrenia, at least in our sample. Further studies in larger samples are warranted.
有人提出,神经肽Y(NPY)活性降低可能与精神分裂症的病理生理学有关。一项尸检研究显示,精神分裂症患者大脑中NPY水平降低。动物大脑以及患者脑脊液中抗精神病药物治疗后NPY水平升高的情况也有报道。此前,伊藤川等人报告称,在日本人群中,NPY基因功能性-485C>T多态性与精神分裂症之间存在正相关。本研究的目的是在一个独立的日本病例对照样本中重复他们的阳性发现。我们的样本包括260例精神分裂症患者(DSM-IV)和196名对照受试者。患者与对照之间在基因型或等位基因频率分布上未观察到显著差异。我们的结果表明,NPY -485C>T多态性可能不会使个体易患精神分裂症,至少在我们的样本中如此。有必要在更大样本中进行进一步研究。