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印度人群代谢综合征中的基因多态性与氧化型低密度脂蛋白水平

Gene Polymorphism and Oxidized LDL Levels in Metabolic Syndrome in Indian Population.

作者信息

Jamatia Elvia, Lali Pramod, Koner B C, Dhanwal D K, Masroor Mirza, Krishnamurthy Kritika, Singh Aditi

机构信息

Department of Biochemistry, Maulana Azad Medical College, New Delhi, India.

Department of Medicine, Maulana Azad Medical College, New Delhi, India.

出版信息

Indian J Endocrinol Metab. 2018 Jul-Aug;22(4):530-534. doi: 10.4103/ijem.IJEM_112_18.

Abstract

OBJECTIVE

Metabolic syndrome (MetS) is associated with abnormal lipid profile and high cardiovascular risk. There is an increased prevalence of coronary artery disease and Type 2 Diabetes Mellitus in India. Oxidized Low Density Lipoprotein Receptor 1(OLR1), a cell surface endocytosis receptor recognize, internalize and degrade oxidized LDL (oxLDL) in vascular endothelium and plays a role in the pathogenesis of atherosclerosis. The aim was to explore the association of OLR1 gene polymorphism and measure the serum levels of ox-LDL in patients with MetS in Indian population.

MATERIALS AND METHODS

Forty cases fulfilling the IDF diagnostic criteria for MetS and 40 healthy controls having similar age and sex ratio were genotyped for OLR1 gene (SNP: IVS4-73C>T , rs3736234) by RFLP-PCR. Serum ox-LDL was estimated by ELISA.Their BP, BMI and waist circumference were measured. Fasting Plasma glucose, Serum Triglyceride and HDL-C were measured.

RESULTS

Serum oxLDL was significantly higher in MetS cases as compared to controls (p < 0.0001). Odds ratio of T allele of above OLR1 SNP among subjects with MetS was 14.79 (95%CI: 1.80-121.2, p < 0.05). But no association was found between the SNP and serum ox-LDL levels. People having TT allele had higher BMI compared to those having CC allele.

CONCLUSION

Ox LDL, being more atherogenic might contribute in the pathogenesis of MetS. The intronic SNP: IVS4-73 C>T of OLR1 gene increases the risk of developing MetS by a yet unknown mechanism that is independent of rise in ox-LDL. This OLR1 SNP probably influences BMI.

摘要

目的

代谢综合征(MetS)与血脂异常及心血管疾病高风险相关。在印度,冠状动脉疾病和2型糖尿病的患病率呈上升趋势。氧化型低密度脂蛋白受体1(OLR1)是一种细胞表面内吞受体,可识别、内化并降解血管内皮中的氧化型低密度脂蛋白(oxLDL),在动脉粥样硬化的发病机制中发挥作用。本研究旨在探讨印度人群中MetS患者OLR1基因多态性的关联,并测定其血清ox-LDL水平。

材料与方法

选取40例符合国际糖尿病联盟(IDF)MetS诊断标准的患者及40例年龄和性别比例相似的健康对照,采用限制性片段长度多态性聚合酶链反应(RFLP-PCR)对OLR1基因(单核苷酸多态性:IVS4-73C>T,rs3736234)进行基因分型。采用酶联免疫吸附测定法(ELISA)检测血清ox-LDL水平。测量其血压、体重指数(BMI)和腰围。检测空腹血糖、血清甘油三酯和高密度脂蛋白胆固醇(HDL-C)水平。

结果

与对照组相比,MetS患者血清oxLDL水平显著升高(p<0.0001)。MetS患者中上述OLR1单核苷酸多态性T等位基因的比值比为14.79(95%置信区间:1.80-121.2,p<0.05)。但未发现该单核苷酸多态性与血清ox-LDL水平之间存在关联。与携带CC等位基因的人相比,携带TT等位基因的人BMI更高。

结论

oxLDL具有更强的致动脉粥样硬化作用,可能在MetS的发病机制中起作用。OLR1基因内含子单核苷酸多态性IVS4-73 C>T通过一种尚不清楚的机制增加了发生MetS的风险,该机制独立于ox-LDL的升高。这种OLR1单核苷酸多态性可能影响BMI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f5/6085951/31c3ef9e9211/IJEM-22-530-g001.jpg

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