class='kwd-title'>Keywords: Acute coronary syndr'/> The association of megalin and cubilin genetic variants with serum levels of 25-hydroxvitamin D and the incidence of acute coronary syndrome in Egyptians: A case control study
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The association of megalin and cubilin genetic variants with serum levels of 25-hydroxvitamin D and the incidence of acute coronary syndrome in Egyptians: A case control study

机译:埃及人megalin和cubulin基因变异与血清25-羟维生素D水平和急性冠状动脉综合征发生率的关系:病例对照研究

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摘要

class="kwd-title">Keywords: Acute coronary syndrome, Cubilin, Egyptians, Megalin, Polymorphisms, Vitamin D receptor class="head no_bottom_margin" id="ab010title">AbstractMegalin and cubilin are two receptors that mediate endocytosis of 25-hydroxyvitamin D (25(OH)D) for its final activation by hydroxylation. The aim of the present study was to evaluate the association of polymorphisms in megalin (rs2075252 and rs4668123) and cubilin (rs1801222 and rs12766939) with the circulating serum levels of 25(OH)D and with the early incidence of acute coronary syndrome (ACS) in Egyptians. The study included 328 subjects; 185 ACS patients aged between 27 and 60 years, and 143 healthy age-matched controls. Genotyping of cubilin rs12766939 Single Nucleotide Polymorphism (SNP) was performed using Real-Time Polymerase Chain Reaction (qPCR) and for megalin rs4668123 and rs2075252 and cubilin rs1801222 by Polymerase Chain Reaction- Restriction Fragment Length Polymorphism (PCR-RFLP). 25(OH)D levels were measured by Ultra Performance Liquid Chromatography- Tandem Mass Spectroscopy (UPLC-MS/MS). Results showed that vitamin D deficiency was highly linked to ACS incidence (P < 0.0001). The megalin rs4668123 CC, cubilin rs1801222 GG and cubilin rs12766939 GG + GA genotypes are associated with a higher ACS incidence and can be considered risk factors, according to Chi-squared test (P = 0.0003, 0.0442, 0.013 respectively). Conversely, the megalin rs2075252 SNP was not associated with increased ACS incidence. However, after performing multiple logistic regression analysis, only the megalin rs4668123 SNP was considered an independent ACS risk factor. Furthermore, the megalin rs4668123 CC genotype was associated with lower 25(OH)D levels (P = 0.0018). In conclusion, megalin rs4668123 (CC) was linked to lower 25(OH)D levels and can be considered an independent risk factor for incidence of ACS.
机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>关键字:急性冠脉综合征,西比林,埃及人,Megalin,多态性,维生素D受体 class =“ head no_bottom_margin“ id =” ab010title“>摘要麦加林和cubilin是介导25-羟基维生素D(25(OH)D)的内吞作用的两个受体,其通过羟基化作用最终活化。本研究的目的是评估megalin(rs2075252和rs4668123)和cubilin(rs1801222和rs12766939)多态性与循环血清25(OH)D水平和急性冠状动脉综合征(ACS)的早期发病率之间的关系在埃及人中。这项研究包括328个受试者。 185位年龄在27至60岁之间的ACS患者和143位年龄匹配的健康对照者。使用实时聚合酶链反应(qPCR)对Cubilin rs12766939单核苷酸多态性(SNP)进行基因分型,对megalin rs4668123和rs2075252和cubilin rs1801222进行聚合酶链反应-限制性片段长度多态性(PCR-RFLP)。通过超高效液相色谱-串联质谱法(UPLC-MS / MS)测量25(OH)D水平。结果表明,维生素D缺乏与ACS的发生密切相关(P <0.0001)。根据卡方检验,megalin rs4668123 CC,cubilin rs1801222 GG和cubilin rs12766939 GG + GA基因型与较高的ACS发病率相关,并且可以视为危险因素(分别为P = 0.0003、0.0442、0.013)。相反,megalin rs2075252 SNP与ACS发生率增加无关。但是,在执行多元逻辑回归分析后,仅将巨蛋白rs4668123 SNP视为独立的ACS危险因素。此外,megalin rs4668123 CC基因型与较低的25(OH)D水平相关(P = 0.0018)。总之,megalin rs4668123(CC)与较低的25(OH)D水平相关,可以认为是ACS发生的独立危险因素。

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