rs780094和rs1260326葡萄糖激酶调节蛋白基因多态性与塞尔维亚急性缺血性脑卒中患者血脂异常的关系

Pub Date : 2022-01-01 DOI:10.2298/abs211126002b
J. Bašić, V. Milošević, Milica Živanović, Jasen Kundalić, M. Despotović, T. Jevtović-Stoimenov, I. Stojanovic
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引用次数: 0

摘要

尽管葡萄糖激酶调节蛋白基因(GCKR)的rs780094和rs1260326遗传变异可能与脂质谱失衡有关,但它们对急性缺血性卒中(AIS)风险的影响尚未确定。本研究旨在探讨GCKR单核苷酸多态性(snp) rs780094和rs1260326对AIS患者血脂参数的影响,并评价这些snp与AIS风险的相关性。在一项病例对照研究中,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对148名受试者进行GCKR rs780094和rs1260326 snp的筛选。根据血清总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)和甘油三酯(TG)浓度测定脂质谱。与对照组相比,AIS患者中rs780094T和rs1260326T等位基因的频率显著降低。与野生型携带者相比,rs780094TT基因型和rs1260326TT基因型与AIS风险降低相关。综上所述,本研究首次表明rs780094和rs1260326纯合次要等位基因携带者的AIS风险降低不是由血脂异常引起的,而可能是由于凝血因子糖基化不足引起的。
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Association of rs780094 and rs1260326 glucokinase regulatory protein gene polymorphisms with dyslipidemia in a group of Serbian acute ischemic stroke patients
Although genetic variations rs780094 and rs1260326 of the glucokinase regulatory protein gene (GCKR) could be associated with lipid profile imbalance, their influence on acute ischemic stroke (AIS) risk has not yet been established. The aim of this study was to investigate the influence of GCKR single nucleotide polymorphisms (SNPs) rs780094 and rs1260326 on lipid profile parameters in patients with AIS, and to evaluate the association of these SNPs with the risk of AIS. In a casecontrol study, a total of 148 subjects were screened for GCKR rs780094 and rs1260326 SNPs using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. The lipid profile was determined based on serum total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and triacylglycerol (TG) concentrations. The frequencies of the minor rs780094T allele and the minor rs1260326T allele were significantly lower in AIS patients compared to controls. The rs780094TT genotype and the rs1260326TT genotype were associated with decreased risk of AIS compared to wildtype carriers. In conclusion, this is the first study implying that decreased risk of AIS in rs780094 and rs1260326 homozygous minor allele carriers is not caused by dyslipidemia, but possibly by the lack of coagulation factor glycosylation.
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