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Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study

机译:长期非编码RNA miR4300Hg多态性与术后恶心和呕吐相关:基因组 - 宽协会研究

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Genetic factors such as single-nucleotide polymorphisms (SNPs) play a key role in the development of postoperative nausea and vomiting (PONV). However, previous findings are not widely applicable to different populations because of population-specific genetic variation. We developed a Japanese-specific DNA microarray for high-throughput genotyping. The aim of the current study was to identify SNPs associated with PONV on a genome-wide scale using this microarray in a sample of Japanese surgical patients. Associations between 659,636 SNPs and the incidence of PONV 24?h after surgery in a limited sample of 24 female patients were assessed using the microarray. After imputation of genotypes at 24,330,529 SNPs, 78 SNPs were found to be associated with the incidence of PONV. We chose 4 of the 78 SNPs to focus on by in silico functional annotation. Finally, we genotyped these 4 candidate SNPs in 255 patients using real-time PCR to verify association with the incidence of PONV. The T C variant of rs11232965 in the long non-coding RNA MIR4300HG was significantly associated with reduced incidence of PONV among genotypes and between alleles (p = 0.01 and 0.007). We identified a novel SNP (rs11232965) in the long non-coding RNA MIR4300HG that is associated with PONV. The rs11232965-SNP variant (T C) is protective against the incidence of PONV. This study was registered at the UMIN Clinical Trials Registry (Identifier: UMIN000022903 , date of registration: June 27, 2016, retrospectively registered.
机译:单核苷酸多态性(SNPs)等遗传因素在术后恶心和呕吐(PONV)的发展中起着关键作用。然而,由于人群特异性遗传变异,之前的发现不广泛适用于不同的群体。我们开发了一种用于高通量基因分型的日本特异性DNA微阵列。目前研究的目的是在日本手术患者样本中使用这种微阵列,鉴定与PONV相关的SNP。使用微阵列评估了24例女性患者的有限样本后的659,636 snps和PONV24Ωh的发病率。在24,330,529处的基因型归咎于SNPS后,发现78个SNP与PONV的发生率有关。我们选择了78个SNP中的4个以在Silico功能注释中专注于。最后,在255名患者中使用实时PCR进行基因对这些4个候选SNP进行核对,以验证与PONV发病率的关联。长期非编码RNA miR4300HG中的T> C变体与基因型之间的痘痘和等位基因之间的痘痘发病率降低(P = 0.01和0.007)显着相关。我们在与PONV相关的长非编码RNA miR4300HG中鉴定了一种新型SNP(RS11232965)。 RS11232965-SNP变体(T> C)对PONV的发生率是保护性。本研究在Umin临床试验登记处注册(标识符:UMIN000022903,注册日期:2016年6月27日,回顾性地注册。

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