The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
Rheumatology Department of the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Clin Exp Immunol. 2018 Jul;193(1):95-102. doi: 10.1111/cei.13121. Epub 2018 Mar 30.
Previous studies show that endoplasmic reticulum-associated aminopeptidase (ERAP1/ERAP2) and runt-related transcription factor 3 (RUNX3) gene polymorphisms are associated with AS (ankylosing spondylitis) in European Caucasians. However, contradictory results were reported in different Asian populations. The purpose of this study was to determine whether eleven candidate single nucleotide polymorphisms (SNPs) in ERAP1/ERAP2 and six in RUNX3 genes confer susceptibility to AS with or without acute anterior uveitis (AAU) [AS AAU or AS AAU ] in Chinese Han. Therefore, a case-control association study was performed in 882 AS AAU , 884 AS AAU and 1727 healthy controls. Genotyping was performed using the iPLEXGold genotyping assay. A meta-analysis was performed to assess the association of polymorphisms of ERAP1 with AS susceptibility in Asian populations. No association was found between SNPs of ERAP1/ERAP2/RUNX3 and susceptibility of AS with or without AAU. A case-control study between patients with human leucocyte antigen HLA-B27-positive and healthy controls also failed to demonstrate an association of the tested SNP with AS with or without AAU. Moreover, a meta-analysis showed that there was no association of rs30187, rs27037, rs27980, rs27434 and rs27582 in ERAP1 with AS in Chinese Han. Taken together, 17 SNPs in ERAP1/ERAP2 and RUNX3 genes did not confer disease susceptibility to AS in Chinese Han.
先前的研究表明内质网相关氨肽酶 (ERAP1/ERAP2) 和 runt 相关转录因子 3 (RUNX3) 基因多态性与欧洲白种人中的 AS(强直性脊柱炎)有关。然而,不同的亚洲人群中报告了相互矛盾的结果。本研究的目的是确定 ERAP1/ERAP2 中的 11 个候选单核苷酸多态性 (SNP) 和 RUNX3 基因中的 6 个是否与中国汉族人群中有无急性前葡萄膜炎 (AAU) 的 AS (AS AAU 或 AS AAU) 易感性相关。因此,对 882 例 AS AAU、884 例 AS AAU 和 1727 例健康对照进行了病例对照关联研究。使用 iPLEXGold 基因分型检测进行基因分型。进行荟萃分析以评估 ERAP1 多态性与亚洲人群 AS 易感性的相关性。未发现 ERAP1/ERAP2/RUNX3 单核苷酸多态性与 AS 有无 AAU 的易感性之间存在关联。HLA-B27 阳性患者与健康对照者之间的病例对照研究也未能证明所检测 SNP 与 AS 有无 AAU 有关。此外,荟萃分析表明,ERAP1 中的 rs30187、rs27037、rs27980、rs27434 和 rs27582 与中国汉族人群的 AS 无关。综上所述,ERAP1/ERAP2 和 RUNX3 基因中的 17 个 SNP 并未赋予中国汉族人群 AS 的疾病易感性。