Suppr超能文献

新疆汉族和维吾尔族人群脂质代谢相关基因多态性与缺血性脑卒中的关联

The association of lipid metabolism relative gene polymorphisms and ischemic stroke in Han and Uighur population of Xinjiang.

作者信息

Yue Yun-Hua, Liu Ling-Yun, Hu Liang, Li You-Mei, Mao Jie-Ping, Yang Xiao-Ying, Dila Na-Mu

机构信息

Department of Neurology, Yangpu Hospital Tongji University School of Medicine, No. 450 Tengyue Road, Shanghai, 200090, China.

Department of Neurology, Friendship Hospital to Urumqi, Urumqi, 830049, China.

出版信息

Lipids Health Dis. 2017 Jun 17;16(1):120. doi: 10.1186/s12944-017-0491-9.

Abstract

BACKGROUND

The present study is aimed to evaluate difference of lipid metabolism related gene single nucleotide polymorphisms (SNPs) with ischemic stroke (IS) in Han and Uighur population of Xinjiang, China.

METHODS

Four hundred eight patients with ischemic stroke and 347 unrelated healthy individuals of age and sex matched were genotyped for Apolipoprotein A5 (ApoA5), lipoprotein lipase (LPL), Cholesteryl ester transfer protein (CETP) and low-density lipoprotein receptor (LDL-R) genes. Their mutation difference was analyzed by SNaP shot techniques. GeneMapper4.1 SPSS20.0 software was used for data management and analysis. Using a single locus analysis, the distribution difference of genotype loci in ischemic stroke cases and controls were detected to assess the genetic risk factors of ischemic stroke.

RESULTS

Significance differences of genotype distribution in ischemic stroke cases and controls were observed in LDLR rs688 in Han and Uighur population in recessive model from analysis of single gene locus. It also was found that dramatic difference of triglyceride (TG) of LPL rs328 and systolic blood pressure in CETP rs708277 of total population. In binary logistic regression analysis of total studied population, ischemic stroke was observed significantly associated with LDLR rs688 both addictive model (TT/CC, adjusted OR = 1.47, 95% CI = 1.04-2.07) and recessive model (TT/CT + CC, adjusted Odds ratio (OR) = 2.66, 95% Confidence Interval (CI) = 1.37-5.14). In Han population, ischemic stroke was observed significantly associated with rs688 both in addictive model (TT/CC, adjusted OR = 3.27, 95% CI = 1.06-10.05). In Uighur population, no significant association was found between gene polymorphisms and the risk of ischemic stroke. Combined analysis of multiple gene and loci, interaction effects of LDLR rs688 C/T, ApoA5 rs662799 A/G and CETP rs708272 C/T denoted a significant influence on IS susceptibility.

CONCLUSION

Single nucleotide polymorphisms of lipid metabolism relative gene were significantly associated with the morbidity of ischemic stroke in Han population. The interaction effects of rs688 C/T with ApoA5 rs662799 A/G and CETP rs708272 C/T promoted the occurrence of IS.

摘要

背景

本研究旨在评估中国新疆汉族和维吾尔族人群中脂质代谢相关基因单核苷酸多态性(SNP)与缺血性脑卒中(IS)的差异。

方法

对408例缺血性脑卒中患者和347例年龄、性别匹配的无血缘关系健康个体进行载脂蛋白A5(ApoA5)、脂蛋白脂肪酶(LPL)、胆固醇酯转运蛋白(CETP)和低密度脂蛋白受体(LDL-R)基因的基因分型。采用SNaP shot技术分析其突变差异。使用GeneMapper4.1和SPSS20.0软件进行数据管理和分析。通过单基因座分析,检测缺血性脑卒中病例组和对照组中基因型位点的分布差异,以评估缺血性脑卒中的遗传危险因素。

结果

单基因座分析显示,汉族和维吾尔族人群中,LDLR rs688在隐性模型下,缺血性脑卒中病例组和对照组的基因型分布存在显著差异。还发现,总体人群中LPL rs328的甘油三酯(TG)和CETP rs708277的收缩压存在显著差异。在总体研究人群的二元逻辑回归分析中,缺血性脑卒中与LDLR rs688在相加模型(TT/CC,校正OR = 1.47,95%CI = 1.04 - 2.07)和隐性模型(TT/CT + CC,校正比值比(OR) = 2.66,95%置信区间(CI) = 1.37 - 5.14)下均显著相关。在汉族人群中,缺血性脑卒中与rs688在相加模型(TT/CC,校正OR = 3.27,95%CI = 1.06 - 10.05)下也显著相关。在维吾尔族人群中,未发现基因多态性与缺血性脑卒中风险之间存在显著关联。多基因和多位点联合分析显示,LDLR rs688 C/T、ApoA5 rs662799 A/G和CETP rs708272 C/T的相互作用对IS易感性有显著影响。

结论

脂质代谢相关基因的单核苷酸多态性与汉族人群缺血性脑卒中的发病显著相关。rs688 C/T与ApoA5 rs662799 A/G和CETP rs708272 C/T的相互作用促进了IS的发生。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验