Karban Amir, Feldman Tzah, Waterman Matti, Leiba Ronit, Efrati Edna
Department of Internal Medicine C, Rambam Health Care Campus Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology Laboratory of Toxicology, Pharmacology and Pharmacogenetics, Israel Poison Information Center, Rambam Health Care Campus Department of Gastroenterology, Rambam Health Care Campus Epidemiologic Unit, Rambam Health Care Campus, Haifa, Israel.
Medicine (Baltimore). 2016 Dec;95(51):e5611. doi: 10.1097/MD.0000000000005611.
MTHFR C677T is a common gene polymorphism that has been shown to be associated with hyperhomocysteinemia. Studies on the role of MTHFR in inflammatory bowel diseases (IBD) have yielded conflicting results, perhaps due in part to genetic heterogeneity. The prevalence of the MTHFR C677T variant allele varies according to Jewish subpopulations: Ashkenazi vs non-Ashkenazi. The aim of this study was to examine the association between MTHFR C677T genotype and IBD in the different Jewish populations.DNA samples were assessed for the presence of the MTHFR C677T variant allele in 445 Jewish Israeli IBD patients: 338 with Crohn's disease [CD] (214 Ashkenazi and 124 non-Ashkenazi Jews) and 107 with ulcerative colitis [UC] (73 Ashkenazi and 34 non-Ashkenazi Jews), and in 347 healthy controls: 173 Ashkenazi and 174 Non-Ashkenazi Jews. Possible genotype-phenotype associations were investigated.We showed a significantly higher frequency of MTHFR 677T variant genotypes in non-Ashkenazi CD patients: Odds ratio of 1.86 for heterozygotes (CT) and 2.89 for homozygotes (TT) compared to non-Ashkenazi healthy controls. No significant association was found for UC in non-Ashkenazi patients or for CD or UC in Ashkenazi patients.Our findings suggest that the MTHFR 677T variant may contribute to the risk of CD in non-Ashkenazi but not Ashkenazi Jews. This may result from genetic heterogeneity and highlights the complexity of the genetic etiology of IBD.
亚甲基四氢叶酸还原酶(MTHFR)C677T是一种常见的基因多态性,已被证明与高同型半胱氨酸血症有关。关于MTHFR在炎症性肠病(IBD)中的作用的研究结果相互矛盾,这可能部分归因于基因异质性。MTHFR C677T变异等位基因的患病率因犹太亚群体而异:阿什肯纳兹犹太人与非阿什肯纳兹犹太人。本研究的目的是检验不同犹太人群中MTHFR C677T基因型与IBD之间的关联。对445名以色列犹太IBD患者的DNA样本进行评估,以检测MTHFR C677T变异等位基因的存在:338例克罗恩病(CD)患者(214例阿什肯纳兹犹太人和124例非阿什肯纳兹犹太人)和107例溃疡性结肠炎(UC)患者(73例阿什肯纳兹犹太人和34例非阿什肯纳兹犹太人),以及347名健康对照者:173例阿什肯纳兹犹太人和174例非阿什肯纳兹犹太人。研究了可能的基因型-表型关联。我们发现,非阿什肯纳兹CD患者中MTHFR 677T变异基因型的频率显著更高:与非阿什肯纳兹健康对照者相比,杂合子(CT)的优势比为1.86,纯合子(TT)的优势比为2.89。在非阿什肯纳兹患者的UC中或阿什肯纳兹患者的CD或UC中未发现显著关联。我们的研究结果表明,MTHFR 677T变异可能是非阿什肯纳兹犹太人而非阿什肯纳兹犹太人患CD风险的一个因素。这可能是由于基因异质性导致的,并突出了IBD遗传病因的复杂性。