Scolaro Bruno Lorenzo, dos Santos Emily, Ferreira Leslie Ecker, França Paulo Henrique Condeixa de, Kleinubing Harry, Kotze Paulo Gustavo, Pinho Mauro de Souza Leite
Universidade da Região de Joinville - UNIVILLE, Joinville, SC, Brasil.
Departamento de Medicina da Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brasil.
Arq Gastroenterol. 2014 Apr-Jun;51(2):97-101. doi: 10.1590/s0004-28032014000200005.
Crohn's disease is characterized by a chronic and debilitating inflammatory disorder of the gastrointestinal tract. Several factors may contribute to its development. From extensive studies of the human genome, the polymorphism T300A of the gene ATG16L1 (autophagy-related 16-like 1) has been related to increased risk of developing this disease.
Analyze the role of polymorphism T300A (rs2241880) in patients with Crohn's disease.
238 samples from (control group) and 106 samples from patients with Crohn's disease recruited at five Southern Brazilian reference centers were evaluated. The genotyping consisted of the amplification via Polymerase Chain Reaction of the genomic segment encompassing T300A, followed by Restriction Fragment Length Polymorphism analysis. The amplicons and fragments were separated by agarose gel electrophoresis and confirmed under ultraviolet light.
The genotype AG was more prevalent among patients and controls (50% vs 44.8%), followed by genotypes AA (26.4% vs 35.1%) and GG (23.6% vs 20.1%). The frequency of the allele G of the polymorphism T300A was higher in the group of patients with Crohn's disease (48.6%) than in controls (42.4%), although not reaching statistical significance.
It was not possible to confirm the increased susceptibility on development of Crohn's disease conferred by polymorphism T300A.
克罗恩病的特征是胃肠道慢性衰弱性炎症性疾病。有几个因素可能导致其发病。通过对人类基因组的广泛研究,自噬相关16样蛋白1(ATG16L1)基因的T300A多态性与患此病的风险增加有关。
分析T300A(rs2241880)多态性在克罗恩病患者中的作用。
对巴西南部五个参考中心招募的238份(对照组)样本和106份克罗恩病患者样本进行了评估。基因分型包括通过聚合酶链反应扩增包含T300A的基因组片段,随后进行限制性片段长度多态性分析。扩增子和片段通过琼脂糖凝胶电泳分离,并在紫外线下确认。
基因型AG在患者和对照组中更为普遍(50%对44.8%),其次是基因型AA(26.4%对35.1%)和GG(23.6%对20.1%)。T300A多态性的等位基因G在克罗恩病患者组中的频率(48.6%)高于对照组(42.4%),尽管未达到统计学显著性。
无法证实T300A多态性会增加患克罗恩病的易感性。