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Association of integrin-ß2 polymorphism and expression with the risk of rheumatoid arthritis and osteoarthritis in Egyptian patients.
Selim, Aliaa M; Elsabagh, Yumn A; El-Sawalhi, Maha M; Ismail, Nabila A; Senousy, Mahmoud A.
Afiliación
  • Selim AM; Department of Biochemistry, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt. aliaa.mohamed@pharma.cu.edu.eg.
  • Elsabagh YA; Department of Rheumatology and Clinical Immunology, Internal Medicine, Kasr Al- Ainy, Faculty of Medicine, Cairo University, Cairo, Egypt.
  • El-Sawalhi MM; Department of Biochemistry, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt. maha.elsawalhi@pharma.cu.edu.eg.
  • Ismail NA; Department of Biochemistry, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt.
  • Senousy MA; Department of Biochemistry, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt.
BMC Med Genomics ; 16(1): 204, 2023 08 29.
Article en En | MEDLINE | ID: mdl-37644537
BACKGROUND: The genetic architecture of rheumatoid arthritis (RA) and osteoarthritis (OA) are still unclear. Although RA and OA have quite different causes, they share synovial inflammation, risk factors, and some disease-associated genes, including the integrin subunit ß2 (ITGB2)/CD18 gene involved in extracellular matrix interactions and immune cell signaling. However, the functional role of ITGB2 genetic variants, its circulating expression pattern, and their clinical usefulness in RA and OA remain unexplored. Our study appraised the association of ITGB2 rs2070946 single nucleotide polymorphism with the vulnerability to RA and OA and its influence on ITGB2 mRNA expression, along with the potential of serum ITGB2 expression in RA and OA diagnosis. METHODS: This study included 70 RA patients, 70 primary OA patients, and 60 healthy volunteers. Genotyping and gene expression analysis were performed using qPCR. Bioinformatics analysis was employed to construct the protein-protein interaction (PPI) network of ITGB2. RESULTS: Serum ITGB2 mRNA expression was upregulated in both RA and OA compared to healthy controls. ITGB2 rs2070946 was associated with escalating risk of both diseases. RA patients harboring the rs2070946 CC or TC + CC genotypes had higher serum ITGB2 expression than the TT genotype carriers. Likewise, OA patients having the minor homozygote CC genotype had higher serum ITGB2 expression than those carrying the TT, TC or TT + TC genotypes. Serum ITGB2 expression showed profound diagnostic potential for RA and OA in receiver-operating characteristic analysis. In RA, serum ITGB2 expression positively correlated with rheumatoid factor and disease activity score 28 (DAS28). The ITGB2-PPI network enriched in cell-cell adhesion, ICAM-3 receptor activity, T-cell activation, leukocyte adhesion, complement binding, and NF-κB, tumor necrosis factor, and interleukin signaling pathways. CONCLUSION: These findings embrace the impact of ITGB2 rs2070946 as a novel genetic biomarker of both RA and OA, which could alter the ITGB2 expression. Serum ITGB2 expression could aid in timely diagnosis of RA and OA.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteoartritis / Artritis Reumatoide Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Africa Idioma: En Revista: BMC Med Genomics Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteoartritis / Artritis Reumatoide Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Africa Idioma: En Revista: BMC Med Genomics Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Reino Unido