Unidad de Investigación Médica en Trombosis, Hemostasia y Aterogénesis, H.G.R. No 1. Dr. "Carlos Mac Gregor Sánchez Navarro" Instituto Mexicano del Seguro Social, Gabriel Mancera No. 222, Colonia Del Valle, CP 03100 Ciudad de México, Mexico.
Servicio de Urgencias, H.G.R. No 1. Dr. "Carlos Mac Gregor Sánchez Navarro" Instituto Mexicano del Seguro Social, Gabriel Mancera No. 222, Colonia Del Valle, CP 03100 Ciudad de México, Mexico.
Gene. 2019 Mar 10;688:163-170. doi: 10.1016/j.gene.2018.11.080. Epub 2018 Dec 4.
The renin-angiotensin system (RAS) is a hormonal signaling mechanism implicated in the atherosclerosis and regulation of blood pressure. Angiotensin-converting enzyme (ACE) a key enzyme in the RAS, plays important roles in vascular remodeling atherosclerosis, and ischemic stroke. The aim of this study was to examine the possible contribution of the I/D in the ACE gene, M235T and T174M in the angiotensinogen (AGT) gene polymorphisms with ischemic stroke in young Mexican population.
A total of 224 patients with diagnosis of idiopathic ischemic stroke ≤45 years of age, and 224 controls matched by age and gender, were recruited from 2006 and 2016. The I/D, M235T and T174M polymorphisms were determined in all participants by PCR-RFLP.
There was a significant difference in the M235T genotype distribution (p = 0.01) and allele frequency between two groups (p = 0.01). Also, we found a significant difference in the T174M genotype distribution (p = 0.01) and the allele frequency between groups; (p = 0.02). In contrast, in I/D polymorphism, there was a similar genotype distribution; (p = 0.20) and allele distribution (p = 0.20). There were independent factors for ischemic stroke: M235T and T174M polymorphisms, smoking, hypertension, and familial history of atherothrombotic disease. The AGT levels were increased in the group of patients with stroke compared with the control group, but the AGT levels were not influenced by the allele or genotype in each polymorphism.
The M235T and T174M polymorphisms represented an increased risk for stroke in young Mexican individuals. In contrast, the I/D was not associated with in the same group of patients. The AGT levels were higher in the acute phase of stroke, but it was not determined by the polymorphisms.
肾素-血管紧张素系统(RAS)是一种与动脉粥样硬化和血压调节有关的激素信号机制。血管紧张素转换酶(ACE)是 RAS 的关键酶,在血管重塑、动脉粥样硬化和缺血性中风中发挥重要作用。本研究旨在探讨 ACE 基因中的 I/D、血管紧张素原(AGT)基因中的 M235T 和 T174M 多态性与年轻墨西哥人群缺血性中风的可能相关性。
2006 年至 2016 年期间,共招募了 224 名年龄≤45 岁的特发性缺血性中风患者和 224 名年龄和性别匹配的对照组。所有参与者均通过 PCR-RFLP 检测 I/D、M235T 和 T174M 多态性。
两组间 M235T 基因型分布(p=0.01)和等位基因频率存在显著差异。此外,我们还发现两组间 T174M 基因型分布(p=0.01)和等位基因频率存在显著差异(p=0.02)。相比之下,在 I/D 多态性中,基因型分布相似(p=0.20),等位基因分布也相似(p=0.20)。独立的缺血性中风危险因素包括:M235T 和 T174M 多态性、吸烟、高血压和动脉粥样硬化血栓性疾病家族史。与对照组相比,中风组的 AGT 水平升高,但每种多态性的等位基因或基因型均未影响 AGT 水平。
M235T 和 T174M 多态性增加了年轻墨西哥个体患中风的风险。相比之下,I/D 与同一组患者无关。中风急性期的 AGT 水平较高,但不能由多态性决定。