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首页> 外文期刊>American Journal of Translational Research >GWAS-linked hot loci predict short-term functional outcome and recurrence of ischemic stroke in Chinese population
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GWAS-linked hot loci predict short-term functional outcome and recurrence of ischemic stroke in Chinese population

机译:GWAS联系的热点预测中国人口中缺血性卒中的短期功能结果和复发

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In the past decade, an increasing number of genome-wide association studies (GWASs) have been applied to ischemic stroke (IS) susceptibility and recovery. In our study, six GWAS-linked hot loci ( ALDH2 rs10744777, HDAC9 rs2107595, ABO rs532436, PATJ rs76221407, LOC105372028 rs1842681 and PTCH1 rs2236406) were selected, genotyped and analyzed in 982 IS patients from northern Chinese population, in order to explore their roles in stroke functional outcome and recurrence risk. We found that PTCH1 rs2236406 was significantly associated with functional outcome after stroke. Further logistic regression analysis revealed the variant genotype TC/CC of rs2236406 as an independent prognostic factor for poor stroke recovery in Chinese population. Meanwhile, we observed that GA/AA genotype of ABO rs532436 was statistically correlated with the increased risk of stroke recurrence, especially for patients with large-artery atherosclerosis. Moreover, multivariate Cox analysis identified ABO rs12342 as an independent predictor for IS recurrence. Further functional annotation analysis demonstrated that rs2236406 and rs2043211 were located in the transcriptionally active region, and could change the regulatory motif, transcription factor binding capacity and expression level of RP11-435O5.5 (antisense to PTCH1) and ABO, respectively. In summary, our results suggested that PTCH1 rs2236406 and ABO rs532436 may be novel genetic markers and potential therapeutic targets for stroke prognosis. More studies are required to confirm our findings and clarify the underlying molecular mechanisms.
机译:在过去十年中,越来越多的基因组关联研究(Gwass)已应用于缺血性卒中(是)易感性和恢复。在我们的研究中,选择了六个GWAS连接的热点(ALDH2 RS1074777,HDAC9 RS2107595,ABO RS532436,POC105372028 RS1842681和PTCH1 RS2236406),基因分型和982年分析,是来自北方人口的患者,以探索其角色中风功能结果和复发风险。我们发现PTCH1 RS2236406与中风后功能结果显着相关。进一步的逻辑回归分析显示,RS2236406的变体基因型TC / CC作为中国人群中风恢复不良的独立预后因素。同时,我们观察到ABO RS532436的GA / AA基因型与中风复发的风险增加,特别是对于大动脉动脉粥样硬化的患者有统计学相关。此外,多元COX分析将ABO RS12342鉴定为复发的独立预测因子。进一步的功能注释分析证明RS2236406和RS2043211位于转录有源区中,并且可以分别改变RP11-43505.5(反义对PTCH1)和ABO的调节基序,转录因子结合能力和表达水平。总之,我们的结果表明,PTCH1 RS2236406和ABO RS532436可以是新的遗传标记和潜在的卒中预后治疗靶标。需要更多的研究来确认我们的发现并澄清潜在的分子机制。

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