Oliver J, Gómez-Garcia M, Vilchez J R, López-Nevot M A, Piñero A, Correro F, Nieto A, Martín J
Instituto de Parasitología y Biomedicina López Neyra, CSIC, Granada, Spain.
Tissue Antigens. 2006 Apr;67(4):326-30. doi: 10.1111/j.1399-0039.2006.00578.x.
To assess the influence of inducible and endothelial nitric oxide synthase gene (NOS2A and NOS3) polymorphisms in susceptibility to Crohn's disease (CD) and ulcerative colitis (UC). A total of 505 inflammatory bowel disease (IBD) patients (221 with UC and 284 with CD) and 332 ethnically matched controls were studied. Patients and controls were genotyped by polymerase chain reaction -based techniques for a multiallelic (CCTTT)(n) repeat and biallelic marker (TAAA)(n) in the promoter region of the NOS2A gene and for a T/C polymorphism at position -786 in the promoter region and a polymorphism in exon 7(298Glu/Asp) of the NOS3 gene. There was not association between NOS2A and NOS3 genotypes, alleles or haplotypes frequencies with UC, CD and controls. Our data suggest that NOS2A and NOS3 polymorphisms do not play a major role in IBD predisposition.
为评估诱导型和内皮型一氧化氮合酶基因(NOS2A和NOS3)多态性对克罗恩病(CD)和溃疡性结肠炎(UC)易感性的影响。共研究了505例炎症性肠病(IBD)患者(221例UC患者和284例CD患者)以及332名种族匹配的对照者。采用基于聚合酶链反应的技术对患者和对照者进行基因分型,检测NOS2A基因启动子区域的多等位基因(CCTTT)(n)重复序列和双等位基因标记(TAAA)(n),以及NOS3基因启动子区域第-786位的T/C多态性和第7外显子(298Glu/Asp)的多态性。NOS2A和NOS3的基因型、等位基因或单倍型频率与UC、CD及对照者之间均无关联。我们的数据表明,NOS2A和NOS3多态性在IBD易感性中不发挥主要作用。