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Published on: October 16, 2016
Association Between miR-155, Its Polymorphism and Ischemia-Modified Albumin in Patients with Rheumatoid Arthritis
Olfat G Shaker1, Omayma O Abdelaleem2, Nermeen A Fouad3
11 Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Abstract:
Rheumatoid arthritis (RA) is a chronic immune-mediated inflammatory disease. We aimed to measure the level of miR-155 and its genetic variant rs767649 in patients with RA and to evaluate their relationship with ischemia-modified albumin (IMA). The study was performed on 79 patients with RA (group I) and 78 healthy control participants (group II). Quantitative real-time polymerase chain reaction was used to assess the expression of serum miR-155 in addition to its functional variant rs767649. IMA levels were measured by enzyme-linked immunosorbent assay. Significant overexpression of miR-155 and higher levels of IMA were detected in patients with RA compared with those in controls (P < 0.0001). The fold change in miR-155 was significantly positively associated with IMA (r = 0.362, P = 0.001) in patients with RA. Significant differences in the frequency of miR-155 (rs767649) genotypes and alleles were noted between patients with RA and controls. MiR-155 and IMA levels were significantly associated with the genotype distribution of miR-155 (rs767649) in patients with RA and were higher in patients with the TT genotype. MiR-155 and its functional variant rs767649 might play an important role in susceptibility to the increased risk of RA, stressing the role of miR-155 as a therapeutic target in the treatment of RA. In addition, IMA levels were increased and correlated with miR-155 and its single nucleotide polymorphism rs767649 in Egyptian patients with RA.
Insights
MicroRNA-155 (miR-155) and ischemia-modified albumin (IMA) are elevated in rheumatoid arthritis (RA) patients. miR-155 and its genetic variant rs767649 are linked to RA risk and severity.
Area of Science:
- Immunology
- Genetics
- Biochemistry
Background:
- Rheumatoid arthritis (RA) is a chronic, immune-mediated inflammatory disease.
- Understanding the molecular mechanisms underlying RA pathogenesis is crucial for developing effective treatments.
- Biomarkers for RA risk and progression are actively sought.
Purpose of the Study:
- To quantify serum miR-155 levels and the miR-155 (rs767649) genetic variant in RA patients.
- To assess the association between miR-155, its genetic variant, and ischemia-modified albumin (IMA) in RA.
- To explore the potential role of miR-155 as a therapeutic target in RA.
Main Methods:
- Quantitative real-time polymerase chain reaction (qPCR) for miR-155 expression and rs767649 genotyping.
- Enzyme-linked immunosorbent assay (ELISA) for measuring IMA levels.
- Comparative analysis between 79 RA patients and 78 healthy controls.
Main Results:
- RA patients exhibited significantly higher miR-155 expression and IMA levels compared to controls (P < 0.0001).
- miR-155 fold change positively correlated with IMA levels (r=0.362, P=0.001) in RA patients.
- Significant differences in miR-155 (rs767649) genotype and allele frequencies were observed between RA patients and controls, with higher levels in the TT genotype.
Conclusions:
- miR-155 and its variant rs767649 may contribute to RA susceptibility and increased risk.
- IMA levels are elevated in RA and correlate with miR-155 and its genetic variant.
- miR-155 represents a potential therapeutic target for rheumatoid arthritis treatment.
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