The P268S and M863V Polymorphisms of the NOD2/CARD15 Gene in Crohn's Disease and Ulcerative Colitis

Diler S. B., POLAT F., Yaras S.

CYTOLOGY AND GENETICS, cilt.53, sa.5, ss.424-429, 2019 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 53 Sayı: 5
  • Basım Tarihi: 2019
  • Doi Numarası: 10.3103/s0095452719050074
  • Dergi Adı: CYTOLOGY AND GENETICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.424-429
  • Anahtar Kelimeler: ulcerative colitis, Crohn's disease, NOD2, CARD15 gene, single nucleotide polymorphism, RFLP, INFLAMMATORY-BOWEL-DISEASE, NOD2 GENE, ASSOCIATION, MUTATIONS, CARD15, ASHKENAZI, GERMAN, HETEROGENEITY, GENOTYPE, JEWS
  • Kocaeli Üniversitesi Adresli: Evet

Özet

We aimed to determine P268S and M863V polymorphisms in NOD2/CARD15 genes associated with an increased risk of developing Crohn's disease (CD) and ulcerative colitis (UC) and to establish correlations between P268S and M863V genotypes in Turkish population. This study included 152 healthy controls and 138 patients (62 CD and 76 UC) with IBD. Our results, the P268S CC genotype was prevalent on patients and controls (45 vs. 66%), followed by genotypes CT (48 vs. 28%) and TT (7 vs. 6%) in CD. The prevalence of genotypes of CC (wild-type), CT (heterozygous mutant) and TT (homozygous mutant) profiles for the P268S polymorphism were 68, 25 and 7% respectively in UC patients, and 66, 28 and 6% respectively in healthy control groups. We were found in wild-type M863V in all subjects and no other mutant band. P268S polymorphism may be associated with CD susceptibility in Turkish population, whereas there is not associated between M863V polymorphisms and patients with IBD in Turkish population.