Micro RNA-146a But Not IRAK1 is Associated with Rheumatoid Arthritis in the Tunisian Population

被引:21
|
作者
Ben Hassine, Hana [1 ]
Boumiza, Asma [1 ]
Sghiri, Rim [1 ]
Baccouche, Khadija [2 ]
Boussaid, Imen [1 ]
Atig, Ahlem [1 ]
Shakoor, Zahid [3 ]
Bouajina, Elyes [2 ]
Zemni, Ramzi [1 ]
机构
[1] Fac Med Sousse, Res Unit UR 807, Immunol Lab, Sousse, Tunisia
[2] Farhat Hached Hosp, Dept Rheumatol, Sousse, Tunisia
[3] King Khalid Hosp, Immunol Lab, Riyadh, Saudi Arabia
关键词
rheumatoid arthritis; IRAK1; miR-146a; rs3027898; rs2910164; KAPPA-B ACTIVATION; C-REACTIVE-PROTEIN; DEFECTIVE INTERLEUKIN-1; KINASE IRAK1; TARGET GENE; MICRORNA-146A; POLYMORPHISM; HAPLOTYPE; TRAF6; PADI4;
D O I
10.1089/gtmb.2016.0270
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Rheumatoid arthritis (RA) is characterized by the production of an array of proinflammatory cytokines through the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B) signaling pathway. The interleukin-1 receptor (IL-1R) and Toll-like receptors contain a common cytoplasmic motif the Toll/IL-1R (TIR) homology domain. This motif is required for NF-kappa B activation. IL-1R-associated kinase 1 (IRAK1) is a key adapter molecule recruited during the signaling cascade of the TIR. Its gene expression is regulated by the micro-RNA (miR)-146a. Objective: We investigated the role of the IRAK1 single-nucleotide polymorphism (SNP) rs3027898 (IRAK1 rs3027898) and the miR-146a SNP rs2910164 (miR-146a rs2910164) in Tunisian patients with RA and their association with C reactive protein (CRP), rheumatoid factor (RF), anticyclic citrullinated peptide (anti-CCP) antibodies, and erosion. Patients and Methods: In a cohort of 172 adult RA patients and 224 matched controls, IRAK1 rs3027898 genotyping was determined by mutagenically separated polymerase chain reaction (MS-PCR) with newly designed primers, and miR-146a rs2910164 genotyping was determined by restriction fragment length polymorphism PCR (RFLP-PCR). Results: The IRAK1 rs3027898A allele was detected in 67% of RA patients and 70% of controls indicating that it is not associated with RA in codominant, dominant, or recessive models even after stratification by age and gender. The miR-146a rs2910164 G allele was detected in 76% of RA patients and 68% of controls, thus the C allele confers some protection based on a dominant model [CC+GC (odds ratio (95% confidence interval) = 0.6 (0.3-0.9), p = 0.03)]. No association with CRP, RF, anti-CCP, or erosion was found for either SNPs. Conclusion: The IRAK1 rs3027898 was not associated with RA, whereas the C allele of miR-146a rs2910164 was found to be protective. Functional studies are required to investigate the exact role of miR-146a rs2910164 during RA.
引用
收藏
页码:92 / 96
页数:5
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