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骨保护素基因多态性与墨西哥梅斯蒂索人群的亚临床动脉粥样硬化相关。

Osteoprotegerin Gene Polymorphisms Are Associated with Subclinical Atherosclerosis in the Mexican Mestizo Population.

作者信息

Cazarín-Santos Benny Giovanni, Pérez-Hernández Nonanzit, Posadas-Sánchez Rosalinda, Vargas-Alarcón Gilberto, Pérez-Méndez Óscar, Rodríguez-Silverio Juan, Roque-Ramírez Bladimir, Borgonio-Cuadra Verónica Marusa, Rodríguez-Pérez José Manuel

机构信息

Departamento de Biología Molecular, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, Mexico.

Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional, Mexico City 11340, Mexico.

出版信息

Diagnostics (Basel). 2022 Jun 10;12(6):1433. doi: 10.3390/diagnostics12061433.

Abstract

Subclinical atherosclerosis (SA) is the presence of coronary calcification in the absence of cardiovascular symptoms, and it usually progresses to atherosclerotic disease. Studies have shown an association of osteoprotegerin gene (OPG) variants with calcification process in cardiovascular diseases; however, to this day there are no studies that evaluate individuals in the asymptomatic stage of atherosclerotic disease. Therefore, the purpose of this study was to analyze the association of four genetic variants and haplotypes of the OPG gene with the development of SA, through TaqMan genotyping assays. We also aimed to identify potential response elements for transcription factors in these genetic variants. The study included 1413 asymptomatic participants (1041 were controls and 372 were individuals with SA). The rs3102735 polymorphism appeared as a protective marker (OR = 0.693; 95% CI = 0.493−0.974; pheterozygote = 0.035; OR = 0.699; 95% CI = 0.496−0.985; pcodominant 1 = 0.040) and two haplotypes were associated with SA, one as a decreased risk: GACC (OR = 0.641, 95% CI = 0.414−0.990, p = 0.045) and another as an increased risk: GACT (OR = 1.208, 95% CI = 1.020−1.431, p = 0.029). Our data suggest a lower risk of SA in rs3102735 C carriers in a representative sample of Mexican mestizo population.

摘要

亚临床动脉粥样硬化(SA)是指在无心血管症状的情况下出现冠状动脉钙化,且通常会发展为动脉粥样硬化疾病。研究表明骨保护素基因(OPG)变体与心血管疾病的钙化过程有关;然而,迄今为止,尚无研究评估处于动脉粥样硬化疾病无症状阶段的个体。因此,本研究的目的是通过TaqMan基因分型检测分析OPG基因的四种遗传变体和单倍型与SA发生发展的关联。我们还旨在确定这些遗传变体中潜在的转录因子反应元件。该研究纳入了1413名无症状参与者(1041名对照者和372名SA患者)。rs3102735多态性表现为一种保护性标志物(OR = 0.693;95% CI = 0.493−0.974;杂合子p = 0.035;OR = 0.699;95% CI = 0.496−0.985;共显性1 p = 0.040),并且两种单倍型与SA相关,一种为风险降低:GACC(OR = 0.641,95% CI = 0.414−0.990,p = 0.045),另一种为风险增加:GACT(OR = 1.208,95% CI = 1.020−1.431,p = 0.029)。我们的数据表明,在墨西哥混血人群的代表性样本中,rs3102735 C携带者患SA的风险较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47dd/9221599/4ee5d7c69bda/diagnostics-12-01433-g001.jpg

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