AI Article Synopsis

  • - A study investigated the association of the CCR6 gene variant rs3093024 with rheumatoid arthritis (RA) in 500 Pakistani individuals (250 RA patients and 250 healthy controls), finding significant differences in genotype and allele frequencies between the two groups.
  • - The results indicated that the A variant of rs3093024 is linked to increased RA risk, while the G variant appears to be protective; a particular focus was placed on the increased AA genotype in patients compared to AG + GG genotypes.
  • - Bioinformatics analysis suggested that the rs3093024 variant could affect gene splicing, potentially impacting the gene's function, leading to recommendations for larger studies and functional research to better understand these findings.

Article Abstract

C-C Chemokine receptor 6 (CCR6), an important protein in inflammatory and immunological responses, has been previously reported to be associated with rheumatoid arthritis (RA). Therefore, in order to replicate these findings, a case-control study was conducted on 500 subjects (including 250 RA patients and 250 healthy controls) of Pakistani origin. The aim of this study was to determine the association of rs3093024 variant with RA and identify its role in splicing events using bioinformatics tools. The clinical and demographic characteristics of the patients were collected using a well-designed questionnaire. The genotype frequencies of rs3093024 variant were determined using tetra-primer ARMS-PCR (amplification of refractory mutation system-polymerase chain reaction) method. A significant difference was found between rs3093024 genotype frequencies [ = 0.0016,  = 12.915]. Similarly, a significant difference in the allele frequencies between RA patients and healthy controls was also observed [ = 0.0003 and OR (95% CI) = 0.63 (0.49-0.80)]. The stratification of patients showed that there was a significant increase in AA genotype against AG + GG in patients [ = 0.0014, OR (95% CI) = 2.0 (1.32-3.02)]. Furthermore, using bioinformatics analysis, it was found that rs3093024 variant might create a potential splicing enhancer motif (SF2/ASF (IgM-BRCA1) with score of 77.92; Threshold 70.53), which might have important impact on the product of this gene. This study suggests that the A variant of rs3093024 variant is significantly associated with RA-risk and its G variant is protective in Pakistani population but a multi-cohort large sized population study is needed to elucidate these results. Moreover, functional studies are needed to highlight the effects of this polymorphism on the function of gene.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715036PMC
http://dx.doi.org/10.1016/j.sjbs.2020.08.045DOI Listing

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