Single nucleotide polymorphisms in cytokine genes and their association with primary Sjögren's syndrome in Saudi patients: A cross-sectional study.
Bashaer AlqahtaniMaha DaghestaniMohammed A OmairFahidah M AlenziEsam H AlhamadYusra TashkandyNashwa OthmanArjumand WarsyRabih HalwaniPublished in: Saudi medical journal (2023)
The CT genotype at -31 (rs1143627) in the IL-1β gene was not associated with a high risk of pSS development in the Saudi population, in contrast to what has been verified in other ethnicities. However, the C allele in rs10488631 in IRF-5 and the A allele in rs12583006 in BAFF were associated.
Keyphrases
- end stage renal disease
- genome wide
- ejection fraction
- newly diagnosed
- chronic kidney disease
- computed tomography
- contrast enhanced
- magnetic resonance
- dendritic cells
- physical activity
- genome wide identification
- magnetic resonance imaging
- saudi arabia
- dna methylation
- rheumatoid arthritis
- disease activity
- image quality
- dual energy
- bioinformatics analysis
- patient reported