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Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients

机译:中国精神分裂症患者抗精神病药诱导的窦性心动过缓的基因组

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Second-generation antipsychotics (SGAs) play a critical role in current treatment of schizophrenia (SCZ). It has been observed that sinus bradycardia, rare but in certain situations life threatening adverse drug reaction, can be induced by SGAs across different schizophrenia populations. However, the roles of genetic factors in this phenomenon have not been studied yet. In the present study, a genome-wide association study of single nucleotide polymorphisms (SNPs) was performed on Chinese Han SCZ patients to identify susceptibility loci that were associated with sinus bradycardia induced by SGAs. This study applied microarray to obtain genotype profiles of 88 Han Chinese SCZ patients. Our results found that there were no SNPs had genome-wide significant association with sinus bradycardia induced by SGAs. The top GWAS hit located in gene KIAA0247 , which mainly regulated by the tumor suppressor P53 and thus plays a role in carcinogenesis based on resent research and it should not be a susceptibility locus to sinus bradycardia induced by SGAs. Using gene-set functional analysis, we tested that if top 500 SNPs mapped genes were relevant to sinus bradycardia. The result of gene prioritization analysis showed CTNNA3 was strongly correlated with sinus bradycardia, hinting it was a susceptibility gene of this ADR. Our study provides a preliminary study of genetic variants associated with sinus bradycardia induced by SGAs in Han Chinese SCZ patients. The discovery of a possible susceptibility gene shed light on further study of this adverse drug reaction in Han Chinese SCZ patients.
机译:第二代抗精神病药(SGAS)在目前治疗精神分裂症(SCZ)中发挥着关键作用。已经观察到窦性计稀有但在某些情况下威胁不良药物反应,可以通过SGA诱导不同的精神分裂症种群。然而,尚未研究遗传因素在这种现象中的作用。在本研究中,对单一核苷酸多态性(SNP)的基因组 - 宽的关联研究是对中国汉族SCZ患者进行的,以鉴定与SGAS诱导的窦性心动过缓相关的易感位点。本研究应用了微阵列,以获得88例汉族SCZ患者的基因型谱。我们的结果发现,没有SNP与SGAS诱导的窦性心动过缓的基因组显着关系。位于基因Kiaa0247的顶部Gwas命中,主要由肿瘤抑制剂P53调节,从而在致癌基础上发挥作用,基于异构研究,不应该是SGAS诱导的窦性心动过缓的敏感性遗迹。使用基因集功能分析,我们测试了,如果前500个SNP映射基因与窦性心动过缓相关。基因优先化分析的结果显示CTNNA3与窦性心动过缓强烈相关,暗示它是该ADR的易感基因。我们的研究提供了与汉族中国SCZ患者中SGAS诱导的窦性心动过缓相关的遗传变异初步研究。发现可能易感性基因脱光的进一步研究汉族患者这种不良药物反应的研究。

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