Gene polymorphisms of angiotensin-converting enzyme and angiotensinogen and risk of idiopathic ischemic stroke

被引:15
|
作者
Isordia-Salas, Irma [1 ]
Santiago-German, David [2 ]
Carolina Cerda-Mancillas, Megan [1 ]
Hernandez-Juarez, Jesus [1 ]
Bernabe-Garcia, Mariela [3 ]
Leanos-Miranda, Alfredo [4 ]
Antonio Alvarado-Moreno, Jose [1 ]
Majluf-Cruz, Abraham [1 ]
机构
[1] Inst Mexicano Seguro Social, Unidad Invest Med Trombosis Hemostasia & Aterogen, HGR 1 Dr Carlos Mac Gregor Sanchez Navarro, Gabriel Mancera 222, Ciudad Real 03100, Spain
[2] Inst Mexicano Seguro Social, Serv Urgencies, HGR 1 Dr Carlos Mac Gregor Sanchez Navarro, Gabriel Mancera 222, Ciudad Real 03100, Spain
[3] Inst Mexicano Seguro Social, Hosp Pediat, Unidad Invest Med Nutr, Cuauthemoc 330, Ciudad Real 06720, Spain
[4] Inst Mexicano Seguro Social, Unidad Invest Med Med Reprod, UMAE HGO 4, Ave Rio Magdalena 289, Ciudad Real 01090, Spain
关键词
I/D; M235T; T174M; Genetic risk; Idiopathic ischemic stroke; MYOCARDIAL-INFARCTION; T174M POLYMORPHISM; ALDOSTERONE SYSTEM; I/D POLYMORPHISM; INSERTION/DELETION POLYMORPHISM; CEREBROVASCULAR-DISEASE; PLASMA ANGIOTENSINOGEN; BRAIN INFARCTION; HEART-DISEASE; ACE GENE;
D O I
10.1016/j.gene.2018.11.080
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective: 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. Materials and methods: 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. Results: 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. Conclusions: 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.
引用
收藏
页码:163 / 170
页数:8
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