State Key Laboratory of Digestive Diseases, Institute of Digestive Diseases and Department of Medicine & Therapeutics, LKS Institute of Health Sciences, CUHK Shenzhen Research Institute, The Chinese University of Hong Kong, Hong Kong.
Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Hong Kong.
J Cell Mol Med. 2018 Apr;22(4):2368-2377. doi: 10.1111/jcmm.13530. Epub 2018 Feb 14.
The incidence of Crohn's disease is increasing in many Asian countries, but considerable differences in genetic susceptibility have been reported between Western and Asian populations. This study aimed to fine-map 23 previously reported Crohn's disease genes and identify their interactions in the Chinese population by Illumina-based targeted capture sequencing. Our results showed that the genetic polymorphism A>G at rs144982232 in MST1 showed the most significant association (P = 1.78 × 10 ; odds ratio = 4.87). JAK2 rs1159782 (T>C) was also strongly associated with Crohn's disease (P = 2.34 × 10 ; odds ratio = 3.72). Gene-gene interaction analysis revealed significant interactions between MST1 and other susceptibility genes, including NOD2, MUC19 and ATG16L1 in contributing to Crohn's disease risk. Main genetic associations and gene-gene interactions were verified using ImmunoChip data set. In conclusion, a novel susceptibility locus in MST1 was identified. Our analysis suggests that MST1 might interact with key susceptibility genes involved in autophagy and bacterial recognition. These findings provide insight into the genetic architecture of Crohn's disease in Chinese and may partially explain the disparity of genetic signals in Crohn's disease susceptibility across different ethnic populations by highlighting the contribution of gene-gene interactions.
克罗恩病在许多亚洲国家的发病率正在上升,但西方和亚洲人群之间的遗传易感性存在相当大的差异。本研究旨在通过基于 Illumina 的靶向捕获测序,对 23 个先前报道的克罗恩病基因进行精细定位,并鉴定其在中国人群中的相互作用。我们的研究结果表明,rs144982232 处的遗传多态性 A>G 与 MST1 表现出最显著的关联(P=1.78×10-8;优势比=4.87)。JAK2 rs1159782(T>C)也与克罗恩病强烈相关(P=2.34×10-8;优势比=3.72)。基因-基因相互作用分析显示,MST1 与其他易感性基因(包括 NOD2、MUC19 和 ATG16L1)之间存在显著的相互作用,这些基因共同影响克罗恩病的发病风险。使用 ImmunoChip 数据集验证了主要的遗传关联和基因-基因相互作用。总之,在 MST1 中确定了一个新的易感位点。我们的分析表明,MST1 可能与参与自噬和细菌识别的关键易感性基因相互作用。这些发现为中国人群克罗恩病的遗传结构提供了深入了解,通过强调基因-基因相互作用的贡献,可能部分解释了不同种族人群中克罗恩病易感性遗传信号的差异。