Song G G, Kim J-H, Lee Y H
Division of Rheumatology, Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, 126-1, Anam-dong 5 ga, Seongbuk-gu, 136-705, Seoul, South Korea.
Z Rheumatol. 2016 May;75(4):406-15. doi: 10.1007/s00393-014-1540-7.
The objective of this study was to determine whether interleukin-1 (IL-1) polymorphisms are associated with susceptibility to vasculitis.
A meta-analysis was conducted to investigate possible associations between IL-1A, IL-1B, and IL-1 receptor antagonist (IL1RN) polymorphisms and vasculitis.
A total of 17 studies involving 1384 vasculitis cases [Behçet's disease (BD), IgA vasculitis, anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), Kawasaki disease (KD), giant cell arteritis, and Takayasu's arteritis] and 2710 controls were included in the meta-analysis. This analysis showed an association between BD and the TT + TC genotypes of the IL-1A-889 C/T polymorphism in the entire study population [odds ratio (OR) = 0.623, 95 % CI = 0.395-0.981, p = 0.045), and a trend toward an association in a Turkish population (OR = 0.578, 95 % CI = 0.331-1.010, p = 0.054). A meta-analysis of the IL1RN polymorphism revealed no association with vasculitis in all study subjects (OR for IL1RN2 = 0.904, 95 % CI = 0.626-1.304, p = 0.588). However, stratification by ethnicity revealed a significant association between the IL1RN2 allele and vasculitis including AAV, BD, KD in Asians (OR = 2.393, 95 % CI = 1.429-4.006, p = 0.001), but not in Caucasian and Turkish populations (OR = 0.776, 95 % CI = 0.487-1.238, p = 0.288; OR = 0.914, 95 % CI = 0.667-1.252, p = 0.576, respectively). No association was found between vasculitis and the IL-1B-511 C/T polymorphism, or the IL-1B+3953 C/T polymorphism.
This meta-analysis suggests that the IL-1A-889 C/T polymorphism is associated with susceptibility to BD, and that the IL1RN*2 allele is associated with susceptibility to vasculitis including AAV, BD, and KD in Asians.
本研究的目的是确定白细胞介素-1(IL-1)基因多态性是否与血管炎易感性相关。
进行一项荟萃分析,以研究IL-1A、IL-1B和白细胞介素-1受体拮抗剂(IL1RN)基因多态性与血管炎之间可能存在的关联。
荟萃分析共纳入17项研究,涉及1384例血管炎病例[白塞病(BD)、IgA血管炎、抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)、川崎病(KD)、巨细胞动脉炎和高安动脉炎]和2710例对照。该分析显示,在整个研究人群中,BD与IL-1A - 889 C/T多态性的TT + TC基因型之间存在关联[比值比(OR)= 0.623,95%置信区间(CI)= 0.395 - 0.981,p = 0.045],在土耳其人群中存在关联趋势(OR = 0.578,95% CI = 0.331 - 1.010,p = 0.054)。对IL1RN基因多态性的荟萃分析显示,在所有研究对象中,其与血管炎无关联(IL1RN2的OR = 0.904,95% CI = 0.626 - 1.304,p = 0.588)。然而,按种族分层显示,IL1RN2等位基因与亚洲人中包括AAV、BD、KD在内的血管炎存在显著关联(OR = 2.393,95% CI = 1.429 - 4.006,p = 0.001),但在白种人和土耳其人群中无关联(OR分别为0.776,95% CI = 0.487 - 1.238,p = 0.288;OR = 0.914,95% CI = 0.667 - 1.252,p = 0.576)。未发现血管炎与IL-1B - 511 C/T多态性或IL-1B + 3953 C/T多态性之间存在关联。
这项荟萃分析表明,IL-1A - 889 C/T多态性与BD易感性相关,且IL1RN*2等位基因与亚洲人中包括AAV、BD和KD在内的血管炎易感性相关。