Yang Xinglong, Liu Chuanxin, Zhang Jinxiang, Han Hongying, Wang Xiuyan, Liu Zhoulin, Xu Yanming
Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
College of Basic and Forensic Medicine, Sichuan University, Chengdu, Sichuan Province, 610041, PR China; Department of Psychiatry, Jining Medical College, Jining, Shandong Province, 272051, PR China.
PLoS One. 2015 Mar 13;10(3):e0119692. doi: 10.1371/journal.pone.0119692. eCollection 2015.
Parkinson's disease (PD) and schizophrenia (SCZ) are frequent central nervous disorders that have unclear etiologies but that show similarities in their pathogenesis. Since elevated histamine levels in the brain have been associated with PD and SCZ, we wanted to explore whether the Thr105Ile substitution in the histamine N-methyltransferase gene (HNMT-Thr105Ile), which impairs histamine degradation, is associated with either disease. We used the ligase detection reaction to genotype a case-control cohort of Han Chinese patients with PD or SCZ and healthy controls at the HNMT-Thr105Ile locus. The Ile allele was associated with reduced risk of PD (OR 0.516, 95% CI 0.318 to 0.838, p = 0.007) and of SCZ (OR 0.499, 95% CI 0.288 to 0.865, p = 0.011). Genotype frequencies and minor allele frequencies were similar between patients and controls when we compared males with females or early-onset patients with late-onset ones. Genotype and allele frequencies were not significantly different between PD patients with dyskinesia and PD patients without dyskinesia. Our results suggest that the heterozygous Thr/Ile genotype at the HNMT-Thr105Ile locus and the minor Ile105 allele protect against PD and SCZ in Han Chinese.
帕金森病(PD)和精神分裂症(SCZ)是常见的中枢神经系统疾病,病因不明,但发病机制存在相似之处。由于大脑中组胺水平升高与PD和SCZ有关,我们想探究组胺N-甲基转移酶基因(HNMT-Thr105Ile)中的苏氨酸105异亮氨酸替代(该替代会损害组胺降解)是否与这两种疾病有关。我们使用连接酶检测反应对一组汉族PD或SCZ患者及健康对照在HNMT-Thr105Ile位点进行基因分型。异亮氨酸等位基因与PD风险降低相关(比值比[OR]0.516,95%置信区间[CI]0.318至0.838,p = 0.007)以及与SCZ风险降低相关(OR 0.499,95% CI 0.288至0.865,p = 0.011)。当我们比较男性与女性或早发型患者与晚发型患者时,患者和对照之间的基因型频率和次要等位基因频率相似。有运动障碍的PD患者和无运动障碍的PD患者之间的基因型和等位基因频率无显著差异。我们的结果表明,在汉族人群中,HNMT-Thr105Ile位点的杂合苏氨酸/异亮氨酸基因型和次要的异亮氨酸105等位基因对PD和SCZ具有保护作用。