Department of Clinical Pharmacy, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Cardiovascular Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
BMC Cardiovasc Disord. 2021 Jun 4;21(1):275. doi: 10.1186/s12872-021-02088-1.
One of the most common causes of death in the world is coronary artery disease (CAD). Estrogen, the most important early sex hormones in women, plays an important role in the risk reduction of cardiovascular disease (CVD). Expression of estrogen as well as its receptors including estrogen receptor alpha (ER1) and estrogen receptor beta (ER2) might have an association with the severity or the complexity of CAD. Since most articles have focused on the relationship between ER1 gene polymorphism and CAD, in this study, we aimed to evaluate the association of two ER2 gene polymorphisms, rs4986938 (AluI) and rs1256049 (RsaI), with the severity of CAD.
148 patients with confirmed CAD who underwent elective percutaneous coronary intervention (PCI) were included in this study. Blood samples were collected before coronary angiography and ER2 gene polymorphisms were analyzed by the PCR-RFLP method. The STNTAX Score (SS), grading system for CAD complexity, was evaluated by an interventional cardiologist who was blinded to other data.
110 men and 38 women were participated in this study. Our results revealed a statistically significant relationship between SS and rs4986938 polymorphism of ER2 in men. In contrast, there was no association between rs1256049 genotypes and SS after performing regression analysis.
Besides to the estrogen level, the genetic variation of its receptors might play an important role in the severity or the complexity of CAD. According to our results, rs4986938 polymorphism of ER2 gene may assert a pivotal role in the severity of CAD in men; however, this assumption needs to be proved in studies with a larger population.
冠状动脉疾病(CAD)是世界上最常见的死亡原因之一。雌激素是女性最重要的早期性激素,在降低心血管疾病(CVD)风险方面发挥着重要作用。雌激素及其受体(包括雌激素受体α(ER1)和雌激素受体β(ER2))的表达可能与 CAD 的严重程度或复杂性有关。由于大多数文章都集中在 ER1 基因多态性与 CAD 之间的关系上,因此在本研究中,我们旨在评估两种 ER2 基因多态性,rs4986938(AluI)和 rs1256049(RsaI)与 CAD 严重程度的相关性。
本研究纳入了 148 例经选择性经皮冠状动脉介入治疗(PCI)证实的 CAD 患者。在冠状动脉造影前采集血样,并通过 PCR-RFLP 方法分析 ER2 基因多态性。由一名介入心脏病学家评估 STNTAX 评分(SS),这是一种 CAD 复杂性的分级系统,该介入心脏病学家对其他数据不知情。
本研究共纳入 110 名男性和 38 名女性。我们的结果表明,SS 与 ER2 基因 rs4986938 多态性在男性中存在统计学显著关系。相比之下,在进行回归分析后,rs1256049 基因型与 SS 之间没有关联。
除了雌激素水平外,其受体的遗传变异可能在 CAD 的严重程度或复杂性中发挥重要作用。根据我们的结果,ER2 基因 rs4986938 多态性可能在男性 CAD 的严重程度中起关键作用;然而,这一假设需要在更大人群的研究中得到证实。