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中国人群中 miR219-1 和 miR137 单核苷酸多态性与精神分裂症易感性的关联。

Association between single nucleotide polymorphisms in MiR219-1 and MiR137 and susceptibility to schizophrenia in a Chinese population.

机构信息

Department of Clinical Laboratory, Affiliated Mental and Health Center of Nantong University, Nantong Fourth People's ​Hospital, Nantong 226001, Jiangsu, China.

Affiliated Mental and Health Center of Nantong University, Nantong Fourth People's Hospital, Nantong 226001, Jiangsu, China.

出版信息

FEBS Open Bio. 2015 Aug 28;5:774-8. doi: 10.1016/j.fob.2015.08.008. eCollection 2015.

Abstract

Schizophrenia is one of the most common mental disorders to severely affect human health worldwide. Single nucleotide polymorphisms (SNPs) within related genes are candidate susceptible factors for the disorder. Rs107822 within MiR219-1 and rs1625579 within MiR137 were genotyped in 589 cases and 622 controls to investigate the possible association between the loci and schizophrenia in a Chinese population. Our results showed significant association between rs107822 and the disorder in allele (C vs. T: adjusted OR = 0.773, 95%CI = 0.655-0.912), co-dominant (TC vs. TT: adjusted OR = 0.734, 95%CI = 0.571-0.943; CC vs. TT: adjusted OR = 0.655, 95%CI = 0.459-0.936), dominant (TC + CC vs. TT: adjusted OR = 0.707, 95%CI = 0.559-0.895), and recessive (CC vs. TC + TT: adjusted OR = 0.724, 95%CI = 0.524-0.999) models, respectively. Meanwhile, negative associations were also observed between rs107822 and the disorder in male and female subgroups, and genotype CC of the locus was significantly associated with a lower positive symptom score of PANSS compared to genotype TT carrier in the cases group. However, we didn't observe a significant association between rs1625579 and the disorder. These findings indicate that rs107822 within MiR219-1 might be involved in pathogenesis of schizophrenia and that genotypes TC, CC and allele C of the locus are protective factors for schizophrenia in a Chinese population.

摘要

精神分裂症是一种最常见的严重影响全球人类健康的精神障碍。相关基因内的单核苷酸多态性(SNPs)是该疾病的候选易感因素。在一个中国人群中,我们对 589 例病例和 622 例对照进行了 MiR219-1 内的 rs107822 和 MiR137 内的 rs1625579 基因分型,以探讨这些基因座与精神分裂症之间的可能关联。我们的结果显示,rs107822 与该疾病在等位基因(C 对 T:调整后的 OR = 0.773,95%CI = 0.655-0.912)、共显性(TC 对 TT:调整后的 OR = 0.734,95%CI = 0.571-0.943;CC 对 TT:调整后的 OR = 0.655,95%CI = 0.459-0.936)、显性(TC + CC 对 TT:调整后的 OR = 0.707,95%CI = 0.559-0.895)和隐性(CC 对 TC + TT:调整后的 OR = 0.724,95%CI = 0.524-0.999)模型中均存在显著关联。同时,我们还观察到 rs107822 与男性和女性亚组疾病之间存在负相关,与病例组 TT 携带者相比,该基因座 CC 基因型与 PANSS 阳性症状评分较低显著相关。然而,我们没有观察到 rs1625579 与疾病之间存在显著关联。这些发现表明,MiR219-1 内的 rs107822 可能参与了精神分裂症的发病机制,并且该基因座的 TC、CC 和等位基因 C 是中国人群精神分裂症的保护因素。

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