Sousa João Adriano, Mendonça Maria Isabel, Serrão Marco, Borges Sofia, Henriques Eva, Freitas Sónia, Tentem Margarida, Santos Marina, Freitas Pedro, Ferreira António, Guerra Graça, Drumond António, Palma Reis Roberto
Centro de Investigação Dra Maria Isabel Mendonça, Hospital Dr Nélio Mendonça, SESARAM, EPERAM, Funchal, Madeira, Portugal.
Hospital Santa Cruz, Centro Hospitalar Lisboa Ocidental, CHLO, Carnaxide, Portugal.
Clin Med Insights Cardiol. 2021 Jul 3;15:11795468211029244. doi: 10.1177/11795468211029244. eCollection 2021.
Evidence points epicardial adipose tissue (EAT) as an emerging cardiovascular risk marker. Whether genetic polymorphisms linked with atherosclerosis are associated with higher EAT is still unknown. We aim to assess the role of genetic burden of atherosclerosis and its association to EAT in a cohort of asymptomatic individuals without coronary disease. A total of 996 participants were prospectively enrolled in a single Portuguese center. EAT volume was measured by Cardiac Computed Tomography and participants were distributed into 2 groups, above and below median EAT. SNPs were genotyped and linked to their respective pathophysiological axes. A multiplicative genetic risk score (mGRS) was constructed, representing the genetic burden of the studied SNPs. To evaluate the association between genetics and EAT, we compared both groups by global mGRS, mGRS by functional axes, and SNPs individually. Individuals above-median EAT were older, had a higher body mass index (BMI) and higher prevalence of hypertension, metabolic syndrome, diabetes, and dyslipidemia. They presented higher GRS, that remained an independent predictor of higher EAT volumes. The group with more EAT consistently presented higher polymorphic burden across numerous pathways. After adjustment, age, BMI, and mGRS of each functional axis emerged as independently related to higher EAT volumes. Amongst the 33 SNPs, MTHFR677 polymorphism emerged as the only significant and independent predictor of higher EAT volumes. Patients with higher polymorphism burden for atherosclerosis present higher EAT volumes. We present the first study in a Portuguese population, evaluating the genetic profile of EAT through GWAS and GRS, casting further insight into this complicated matter.
有证据表明,心外膜脂肪组织(EAT)是一种新出现的心血管风险标志物。与动脉粥样硬化相关的基因多态性是否与较高的EAT相关仍不清楚。我们旨在评估动脉粥样硬化遗传负担在一组无冠心病的无症状个体中的作用及其与EAT的关联。共有996名参与者前瞻性地纳入了葡萄牙的一个单一中心。通过心脏计算机断层扫描测量EAT体积,并将参与者分为两组,EAT高于和低于中位数。对单核苷酸多态性(SNP)进行基因分型,并将其与各自的病理生理轴联系起来。构建了一个乘法遗传风险评分(mGRS),代表所研究SNP的遗传负担。为了评估遗传学与EAT之间的关联,我们通过总体mGRS、按功能轴的mGRS以及逐个SNP对两组进行了比较。EAT高于中位数的个体年龄更大,体重指数(BMI)更高,高血压、代谢综合征、糖尿病和血脂异常的患病率更高。他们的GRS更高,这仍然是EAT体积较大的独立预测因素。EAT较多的组在众多途径中始终呈现出更高的多态性负担。调整后,每个功能轴的年龄、BMI和mGRS与EAT体积较大独立相关。在33个SNP中,MTHFR677多态性是EAT体积较大的唯一显著且独立的预测因素。动脉粥样硬化多态性负担较高的患者EAT体积较大。我们在葡萄牙人群中进行了第一项研究,通过全基因组关联研究(GWAS)和GRS评估EAT的基因特征,对这一复杂问题有了更深入的了解。