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Association of a Mirna-Binding Site Polymorphism in Il-16 Gene With Disease Risk and Clinical Characteristics of Rheumatoid Arthritis and Systemic Lupus Erythematosus Publisher Pubmed



Zeinalzadeh S1 ; Kheradmand N2 ; Rasouli G3 ; Esmaeilzadeh E1 ; Pakzad B4 ; Behroozi J5, 6 ; Chamanara M7, 8 ; Zoshk MY9 ; Ehtesham N1 ; Sabet MN10
Authors
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Authors Affiliations
  1. 1. Fetal Health Research Center, Hope Generation Foundation, Tehran, Iran
  2. 2. Department of Medical Genetics and Molecular Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
  3. 3. Faculty of Basic Sciences, Central Tehran Branch, Islamic Azad University, Isfahan, Iran
  4. 4. Division of Rheumatology, Department of Internal Medicine, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran
  5. 5. Research Center for Cancer Screening and Epidemiology, AJA University of Medical Sciences, Tehran, Iran
  6. 6. Department of Genetics and Advanced Medical Technology, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran
  7. 7. Toxicology Research Center, Aja University of Medical Sciences, Tehran, Iran
  8. 8. Department of Pharmacology, School of Medicine, Aja University of Medical Sciences, Tehran, Iran
  9. 9. Trauma Research Center, Aja University of Medical Sciences, Tehran, Iran
  10. 10. School of Medicine, Aja University of Medical Science, Tehran, Iran

Source: Clinical Rheumatology Published:2022


Abstract

Introduction: /objectives. Single nucleotide polymorphisms (SNPs) located at the 3′-UTR region of the target genes of microRNAs (miRNAs) can dysregulate their expression via disrupting the binding site of miRNAs. Interleukin-16 (IL-16) is involved in the pathogenesis of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). In the current study, we assessed the possible association between rs1131445 polymorphism in IL-16 gene with risk and clinical characteristics of RA and SLE in the Iranian population. Methods: In this case–control study, 120 patients with RA, 120 patients with SLE, and 120 unrelated healthy subjects were collected to estimate rs1131445 (T > C) polymorphism in IL-16 gene using real-time PCR high-resolution melting (HRM) method. Results: Our results demonstrated considerable associations between TC genotype and C allele of rs1131445 with enhanced risk of RA (ORfor TC genotype = 3.01; 95%CI [1.667–5.526], P < 0.001; ORfor C allele = 1.96; 95%CI [1.314–2.941], P < 0.001). Besides, there was a marginal association between CC genotype and increased risk of RA (P: 0.031). However, there was an insignificant correlation between genotypes and allele frequencies of rs1131445 with incidence risk of SLE (P > 0.05). Moreover, stratification analysis indicated that the C allele in rs1131445 was linked with disease activity–associated laboratory parameters such as CRP and ESR in both RA and SLE patients, as well as the higher incidence of neurological symptoms in SLE subjects (P < 0.05). Conclusion: These results proposed a significant association between IL-16 polymorphism and augmented risk of RA and clinical characteristics of RA and SLE. © 2022, The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).
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