The P268S and M863V Polymorphisms of the NOD2/CARD15 Gene in Crohn's Disease and Ulcerative Colitis
Küçük Resim Yok
Tarih
2019
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Allerton Press Inc
Erişim Hakkı
info:eu-repo/semantics/closedAccess
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.
Açıklama
Anahtar Kelimeler
ulcerative colitis, Crohn's disease, NOD2, CARD15 gene, single nucleotide polymorphism, RFLP
Kaynak
Cytology and Genetics
WoS Q Değeri
Q4
Scopus Q Değeri
Q4
Cilt
53
Sayı
5
