Key result
TNFA -857C/T polymorphism shows no overall RA link but TT genotype marks anti-CCP-negative RA.
Why the study?
The association of the -857C/T SNP of the TNFA gene with rheumatoid arthritis and clinical parameters in different populations was unclear.
Is the TNFA -857C/T polymorphism associated with Rheumatoid Arthritis and anti-CCP levels in a Mexican population?
Case-Control (n=470)
Is the TNFA -857C/T polymorphism associated with Rheumatoid Arthritis and anti-CCP levels in a Mexican population?
The TT genotype of the TNFA -857C/T SNP is associated with lower anti-CCP levels and could serve as a candidate marker for anti-CCP-negative RA in the Mexican population.
May support TNFA polymorphism research in RA; leaves open clinical biomarker utility pending replication.
Rheumatoid arthritis (RA) is a chronic inflammatory disease whose association with SNPs has led to the identification of biomarkers in different populations. To determine the association of the -857C/T SNP of the TNFA gene with RA and clinical parameters, 233 RA patients and 237 healthy controls were included in this study. The -857C/T polymorphism was determined using the TaqMan® system and clinical features were also determined. We found that the -857C/T SNP was in Hardy-Weinberg equilibrium. Our results showed no association of the -857C/T SNP with RA; however, RA patients carrying the TT genotype showed lower anti-CCP levels than other groups. Therefore, the TT genotype could be a risk factor for developing anti-CCP-negative RA. Our results suggest that the T allele of the TNFA -857C/T SNP exerts an influence on anti-CCP levels and could be a candidate marker for anti-CCP-negative RA.
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Agraz‐Cibrián et al. (2019) conducted a case-control in Rheumatoid arthritis (n=470). TNFA -857C/T polymorphism vs. Healthy controls and non-TT genotypes was evaluated on Association of the -857C/T SNP of the TNFA gene with RA and clinical parameters. The TNFA -857C/T polymorphism showed no overall association with rheumatoid arthritis, but the TT genotype was associated with lower anti-CCP levels, suggesting a marker for anti-CCP-negative RA.
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