miR-618 rs2682818 C>A 多态性与静脉畸形易感性之间的相关性。

IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xi Lin, Zijian Chen, Guitao Wu, Hua Jiang, Zhenyin Liu
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引用次数: 0

摘要

静脉畸形是最常见的先天性血管畸形,发病率很高。以往的研究证实,miRNA 功能区内的多种多态性与肿瘤易感性有关。我们研究了中国南方人群(1113 名患者和 1158 名对照)中 miR-618 rs2682818 C>A 与静脉畸形发病风险之间的相关性。研究采用实时荧光定量 PCR 技术对 miR-618 rs2682818 C>A 进行 TaqMan 基因分型。miR-618 rs2682818 多态性与静脉畸形的易感性无关(CA/AA vs. CC:调整比值比 [AOR] = 1.00,95% 置信区间 [CI] = 0.81-1.25,p = 0.994;AA vs. CC/CA:AOR = 1.10,95% CI = 0.73-1.65,p = 0.646)。对静脉畸形不同亚型的分层分析表明,rs2682818 C>A 多态性基因型在这些亚型中没有显著差异。我们的研究结果表明,miR-618 rs2682818 C>A 多态性与静脉畸形的易感性无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation between the miR-618 rs2682818 C>A polymorphism and venous malformation susceptibility

Venous malformations are the most common congenital vascular malformations, and the incidence rate is high. Previous studies have confirmed that a variety of polymorphisms within the miRNA functional region are associated with tumor susceptibility. We examined the correlation between miR-618 rs2682818 C>A and risk of developing venous malformation in a southern Chinese population (1113 patients and 1158 controls). TaqMan genotyping of miR-618 rs2682818 C>A was conducted utilizing real-time fluorescent quantitative PCR. The miR-618 rs2682818 polymorphism was not correlated with susceptibility to venous malformation (CA/AA vs. CC: adjusted odds ratio [AOR] = 1.00, 95% confidence interval [CI] = 0.81–1.25, p = 0.994; AA vs. CC/CA: AOR = 1.10, 95% CI = 0.73–1.65, p = 0.646). Stratified analysis of different subtypes of venous malformation revealed that there was no significant difference in the rs2682818 C>A polymorphism genotypes across these subtypes. Our results indicate that miR-618 rs2682818 C>A polymorphism is not correlated with the susceptibility to venous malformation.

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来源期刊
Biotechnology and applied biochemistry
Biotechnology and applied biochemistry 工程技术-生化与分子生物学
CiteScore
6.00
自引率
7.10%
发文量
117
审稿时长
3 months
期刊介绍: Published since 1979, Biotechnology and Applied Biochemistry is dedicated to the rapid publication of high quality, significant research at the interface between life sciences and their technological exploitation. The Editors will consider papers for publication based on their novelty and impact as well as their contribution to the advancement of medical biotechnology and industrial biotechnology, covering cutting-edge research in synthetic biology, systems biology, metabolic engineering, bioengineering, biomaterials, biosensing, and nano-biotechnology.
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