Role of Adiponectin Gene and Receptor Polymorphisms and Their mRNA Levels with Serum Adiponectin Level in Myocardial Infarction.

IF 2.6 Q2 GENETICS & HEREDITY Application of Clinical Genetics Pub Date : 2020-12-18 eCollection Date: 2020-01-01 DOI:10.2147/TACG.S282843
Amany A Saleh, Safaa I Tayel, Awny Gamal Shalaby, Sherin Sobhy El Naidany
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引用次数: 9

Abstract

Background and aim: Genetic factors are vital participants in the development and progression of myocardial infarction (MI). Adiponectin has been assumed to have a protective role in MI and adiponectin receptors variants could be a determinant for atherosclerosis. We aimed to evaluate the prevalence of ADIPOQ (rs2241766) and ADIPOR2 (rs10773989) polymorphisms and their association with mRNA levels and circulatory adiponectin levels in patients with MI.

Subjects and methods: A total of 220 participants were classified into two groups: group 1 included 120 patients with MI, and group 2 involved 100 healthy participants as controls. Genotyping of ADIPOQ (rs2241766) and ADIPOR2 (rs10773989) polymorphisms were analyzed using an allele discrimination assay with real-time PCR and their relative expression or mRNA levels were determined by real-time PCR. Serum adiponectin level was determined using an ELISA technique.

Results: The ADIPOQ rs2241766 GG genotype and G allele and the CC genotype and C allele of ADIPOR2 rs10773989 were significantly prevalent in patients with MI and associated with increased risk of MI. We detected a marked reduction in serum adiponectin, ADIPOQ and ADIPOR2 mRNA levels in patients than control. The GG genotype of ADIPOQ rs2241766 and the CC genotype of ADIPOR2 rs10773989 had the lowest levels of their mRNA and adiponectin level in both patients and controls.

Conclusion: Adiponectin gene and receptor variants are potentially related to MI risk; furthermore, their expressions were markedly depressed in MI which suggests their use as potential biomarkers for MI.

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心肌梗死中脂联素基因和受体多态性及其mRNA水平与血清脂联素水平的关系。
背景与目的:遗传因素是心肌梗死(MI)发生发展的重要因素。脂联素被认为在心肌梗死中具有保护作用,脂联素受体变异可能是动脉粥样硬化的决定因素。我们的目的是评估ADIPOQ (rs2241766)和ADIPOR2 (rs10773989)多态性的患病率及其与心肌梗死患者mRNA水平和循环脂联素水平的关系。对象和方法:总共220名参与者分为两组:组1包括120名心肌梗死患者,组2包括100名健康参与者作为对照。采用实时荧光定量PCR对ADIPOQ (rs2241766)和ADIPOR2 (rs10773989)多态性进行基因分型分析,实时荧光定量PCR检测其相对表达量或mRNA水平。采用ELISA技术测定血清脂联素水平。结果:ADIPOQ rs2241766 GG基因型和G等位基因以及ADIPOR2 rs10773989的CC基因型和C等位基因在心肌梗死患者中显著流行,并与心肌梗死风险增加相关。我们检测到患者血清脂联素、ADIPOQ和ADIPOR2 mRNA水平明显低于对照组。GG基因型ADIPOQ rs2241766和CC基因型ADIPOR2 rs10773989的mRNA和脂联素水平在患者和对照组中均最低。结论:脂联素基因和受体变异与心肌梗死风险有潜在关系;此外,它们在心肌梗死中的表达明显降低,这表明它们可以作为心肌梗死的潜在生物标志物。
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来源期刊
Application of Clinical Genetics
Application of Clinical Genetics Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
5.40
自引率
0.00%
发文量
20
审稿时长
16 weeks
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