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Lack of Association Between Monocyte Chemoattractant Protein-1 (Mcp-1) Gene Promoter Polymorphism and Behcet’S Disease With and Without Ocular Involvement in Iranian Population: A Case–Control Study Publisher Pubmed



Ghaffari Laleh M1 ; Bonyadi M1 ; Shahriyari E1 ; Jabbarpoor Bonyadi MH2 ; Soheilian M2 ; Yaseri M3
Authors
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Authors Affiliations
  1. 1. Faculty of Natural Sciences, Center of Excellence for Biodiversity, University of Tabriz, Tabriz, Iran
  2. 2. Ocular Tissue Engineering Research Center, Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Department of Biostatistics and Epidemiology, Tehran University of Medical Sciences, Tehran, Iran

Source: Current Eye Research Published:2022


Abstract

Purpose: This case-control study aimed to evaluate the possible association of MCP-1 − 2518A/G genetic polymorphism with Behcet’s disease (BD) in the Iranian patients. Materials and methods: This study was performed in 135 Behcet’s patients (51 ocular and 84 non-ocular) and 79 healthy individuals. Peripheral blood samples were genotyped for MCP-1 − 2518A/G using the PCR-RFLP technique. Results: The statistical analysis of MCP-1 − 2518A/G showed no significant differences in genotype/allele frequencies between Behcet’s patients and controls. There was no significant association in genotype/allele frequencies between either ocular or non-ocular BD patients and controls. Also, different genotype/allele frequencies between ocular and non-ocular BD were not statistically significant. Conclusions: In this study, with a threshold P-value of 0.05 and an estimated power of 0.81 to detect a significant association (odds ratio ≥1.2), we did not observe any association of this variant with Behcet's disease. © 2021 Taylor & Francis Group, LLC.