Peng Hsin-Yi, Ku Yu-Chi, Shu Bih-Ching, Lung For-Wey
Department of Psychiatry, Kaohsiung Armed Forces General Hospital, Kaohsiung, Taiwan, ROC;
Int J Biomed Sci. 2008 Sep;4(3):185-91.
Schizophrenia is a multi-factorial genetic disease, and it is caused by a combination of different gene polymorphisms and not individual ones, however, its pathogenesis is still unclear. The purpose of this study was explored the association between the -1082G/A, -819T/C, and -592C/A polymorphisms of interleukin-10 (IL-10) in schizophrenia. A total of 659 schizophrenics were recruited from a teaching hospital, whereas 411 healthy non-schizophrenic individuals were recruited from community in the same geographical area. The -1082G/A, -819T/C and -592C/A polymorphisms were genotyped by using PCR-RFLP, direct sequencing and TaqMan(®) SNP assay. Both maximum likelihood method of UNPHASED program and Bayesian method of PHASE software were utilized for haplotypic analysis. An allelic frequency difference was found between the schizophrenics and community controls at -1082G/A polymorphism of IL-10 promoter (χ(2) =4.678, P=0.031). A haplotype of ACA was observed to be associated with schizophrenia after performing UNPHASED, PHASE and multivariate logistic regression analysis (P<0.001; P=0.001). In addition, the persons who carry haplotype ACA of IL-10 promoter SNPs were estimated for 5.789 fold higher risk to develop schizophrenia than controls. We postulated this haplotype association might due to variant-specific effect on IL-10 gene regulation, which leads to imbalance secretion of Th1/Th2 cytokines. Nevertheless, more detailed mechanism needs to be elucidated in further investigations in order to confirm this hypothesis.
精神分裂症是一种多因素遗传疾病,它由不同基因多态性共同作用而非单个基因多态性引起,然而其发病机制仍不清楚。本研究旨在探讨白细胞介素-10(IL-10)基因启动子区-1082G/A、-819T/C和-592C/A多态性与精神分裂症的相关性。我们从一所教学医院招募了659例精神分裂症患者,同时从同一地理区域的社区招募了411名健康非精神分裂症个体。采用聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)、直接测序法和TaqMan(®)SNP分型技术对-1082G/A、-819T/C和-592C/A多态性进行基因分型。运用UNPHASED软件的最大似然法和PHASE软件的贝叶斯法进行单倍型分析。结果发现,精神分裂症患者与社区对照组在IL-10启动子区-1082G/A多态性上存在等位基因频率差异(χ(2)=4.678,P=0.031)。经UNPHASED、PHASE软件分析及多因素logistic回归分析,发现单倍型ACA与精神分裂症相关(P<0.001;P=0.001)。此外,携带IL-10启动子区单倍型ACA的个体患精神分裂症的风险估计是对照组的5.789倍。我们推测这种单倍型关联可能是由于对IL-10基因调控的变异特异性效应,导致Th1/Th2细胞因子分泌失衡。然而,需要进一步深入研究以阐明更详细的机制来证实这一假说。