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Evaluation of Errfi1 +808 T/G Variant and Its Mrna Expression in Coronary Artery In-Stent Restenosis Publisher



Mehrpooya M1 ; Asgarbeik S2 ; Vahidi A1 ; Amoli MM1 ; Hosseini SK3
Authors
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Authors Affiliations
  1. 1. Metabolic Disorders Research Cente, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Cardiovascular Disorders, Division of Interventional Cardiology, Tehran University of Medical Sciences, Tehran, Iran

Source: Gene Reports Published:2021


Abstract

Background: One of the common treatments in cardiovascular disease as the first cause of death in the world is stent implantation. In-Stent Restenosis (ISR) is the major drawback of stent implantation. As there are several lines of evidence suggesting genetic factors involved in ISR, in this study we evaluated the potential role of +808T/G polymorphism in ERRFI1 and its quantitative expression in the development of ISR. Material and methods: Individuals with ISR (n = 41) cases and Non-ISR (n = 51) controls, participated in this study. ERRFI1 gene expression in fresh un-stimulated PBMCs was determined in each group using quantitative real-time PCR. DNA extraction from the whole blood was performed using the phenol-chloroform method. The frequency of genotypes was determined by the PCR-RFLP technique. Results: In spite of the higher amount of ERRFI1 expression in the control group (non-ISR), there were no statistically significant differences between ISR and non-ISR groups (p > 0.05). The expression of ERRFI1 was significantly different between ISR and Non-ISR groups only in patients with diabetes (p < 0.05). A significant association was observed between +808T/G variant and ISR in patients with metabolic syndrome (p < 0.05). Conclusions: The result of this study is suggesting that ERRFI1 gene expression may be associated with ISR in patients with diabetes. Therefore, ERRFI1 can be regarded as a target gene for therapeutic approaches. In addition, our data suggest a protective role for ERRFI1+808 T/G variant in the development of ISR in patients with metabolic syndrome. © 2021