Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.
Department of Rheumatism and Immunity, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Genes Immun. 2017 Jan;18(1):42-47. doi: 10.1038/gene.2016.48. Epub 2016 Dec 29.
It is known that ankylosing spondylitis (AS) and inflammatory bowel disease (IBD) shared a common genetic component. The gist of current study is to assess the role of IBD-associated autophagy gene IRGM on AS susceptibility in a Chinese Han population. A total of 1270 unrelated subjects (643 AS and 627 controls) were enrolled. Two tag single-nucleotide polymorphisms (SNPs) (rs10065172 and rs4958846) were selected and were genotyped by iMLDR Assay technology. Genotypes and haplotype analysis were conducted by using SPSS 16.0 and haploview 4.2 software. Among two tag SNPs of IRGM, no correlation was observed between rs10065172 and AS susceptibility. For rs4958846, genotype and allelic frequencies were marginally discrepant between female cases and controls before, not after, Bonferroni correction (P=0.049; P=0.031). Logistic regression analysis revealed that carriers with CT+TT or CT genotype had a significantly decreased risk for developing AS among female subjects when compared with CC genotype (OR=0.514, 95% CI=0.301-0.876, P=0.014; OR=0.518, 95% CI=0.297-0.902, P=0.020, respectively). Additionally, a risk haplotype rs4958846-rs10065172 (OR=2.093, 95% CI=1.301-3.368) and a protective haplotype rs4958846-rs10065172 (OR=0.652, 95% CI=0.441-0.964) were also identified to be associated with female AS. IBD-associated IRGM gene is also associated with AS susceptibility in the Chinese female population, indicating that autophagy pathway may involve in AS genetic predisposition.
已知强直性脊柱炎(AS)和炎症性肠病(IBD)具有共同的遗传成分。本研究的主旨是评估 IBD 相关自噬基因 IRGM 在中国汉族人群中对 AS 易感性的作用。共纳入 1270 名无关个体(643 例 AS 和 627 例对照)。选择了两个标记单核苷酸多态性(SNP)(rs10065172 和 rs4958846),并通过 iMLDR 检测技术进行了基因分型。使用 SPSS 16.0 和 haploview 4.2 软件进行基因型和单倍型分析。在 IRGM 的两个标记 SNP 中,rs10065172 与 AS 易感性之间没有相关性。对于 rs4958846,在 Bonferroni 校正之前,女性病例和对照组之间的基因型和等位基因频率存在差异,但校正后无差异(P=0.049;P=0.031)。Logistic 回归分析显示,与 CC 基因型相比,女性患者中 CT+TT 或 CT 基因型携带者发生 AS 的风险显著降低(OR=0.514,95%CI=0.301-0.876,P=0.014;OR=0.518,95%CI=0.297-0.902,P=0.020)。此外,还鉴定出一个风险单倍型 rs4958846-rs10065172(OR=2.093,95%CI=1.301-3.368)和一个保护单倍型 rs4958846-rs10065172(OR=0.652,95%CI=0.441-0.964)与女性 AS 相关。IBD 相关的 IRGM 基因也与中国女性人群中的 AS 易感性相关,表明自噬途径可能参与 AS 的遗传易感性。