Department of Gastroenterology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China (mainland).
Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Guangzhou, Guangdong, China (mainland).
Med Sci Monit. 2019 Dec 17;25:9637-9650. doi: 10.12659/MSM.917244.
BACKGROUND Although 90 susceptibility loci of Crohn's disease (CD) have been confirmed in the Asian population, susceptibility genes for perianal fistula of CD (pCD) in this population remain unknown. This study explored susceptibility genes for CD and pCD in the Han population from South China. MATERIAL AND METHODS In total, 490 patients diagnosed with CD between July 2012 and June 2016 at the Sixth Affiliated Hospital of Sun Yat-sen University were included and divided into the CD group (n=240) and the pCD group (n=250). The healthy control group was composed of 260 volunteers. Peripheral blood samples were taken, and single nucleotide polymorphism (SNP) locus sequencing was used to screen for susceptibility loci. SNPs were sequenced using matrix-assisted laser desorption ionization time-of-flight mass spectrometry. RESULTS Nine SNPs in TNFSF1 on chromosome 9 were associated with CD. Among them, the rs6478106 locus is a risk locus for CD. The distribution frequency of the T allele of the rs6478106 SNP was significantly different between cases and controls (32.49% versus 18.27%, P<0.001). Rs72553867, located in the IRGM gene on chromosome 5, rs4409764, located in the NKX2-3 gene on chromosome 10, and rs3731772, located in the AOX1 gene on chromosome 2, were susceptibility factors for pCD. Nine SNPs located in TNFSF15 on chromosome 9 were related to CD in Han individuals from Southern China. CONCLUSIONS The rs6478106 T allele is associated with the risk of CD in the investigated population. SNPs rs72553867 (IRGM gene), rs4409764 (NKX2-3 gene), and rs3731772 (AOX1 gene) increase the risk of pCD.
虽然亚洲人群中已经确定了 90 个克罗恩病(CD)的易感基因,但该人群中 CD 肛周瘘的易感基因仍不清楚。本研究旨在探讨中国南方汉族人群 CD 和 pCD 的易感基因。
共纳入 2012 年 7 月至 2016 年 6 月在中山大学附属第六医院确诊的 490 例 CD 患者,分为 CD 组(n=240)和 pCD 组(n=250)。健康对照组由 260 名志愿者组成。采集外周血样本,进行单核苷酸多态性(SNP)位点测序,筛选易感基因。SNP 采用基质辅助激光解吸电离飞行时间质谱法测序。
9 号染色体上的 TNFSF1 中的 9 个 SNP 与 CD 相关。其中,rs6478106 位点是 CD 的风险位点。rs6478106 SNP 的 T 等位基因在病例组和对照组之间的分布频率差异有统计学意义(32.49%比 18.27%,P<0.001)。rs72553867 位于 5 号染色体上的 IRGM 基因,rs4409764 位于 10 号染色体上的 NKX2-3 基因,rs3731772 位于 2 号染色体上的 AOX1 基因,是 pCD 的易感因素。9 个位于 9 号染色体上的 TNFSF15 的 SNP 与中国南方汉族人群的 CD 相关。
在本研究人群中,rs6478106 T 等位基因与 CD 的发病风险相关。SNP rs72553867(IRGM 基因)、rs4409764(NKX2-3 基因)和 rs3731772(AOX1 基因)增加了 pCD 的风险。