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IL1R 多态性与伊朗强直性脊柱炎 HLA-B27 阳性患者的相关性。

Association of IL1R polymorphism with HLA-B27 positive in Iranian patients with ankylosing spondylitis.

机构信息

Molecular Immunology Research Center, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Department of Immunology, School of Medicine, Tehran University of Medical Sciences.

出版信息

Eur Cytokine Netw. 2011 Dec;22(4):175-80. doi: 10.1684/ecn.2011.0293.

Abstract

Ankylosing spondylitis (AS) is one of the most common causes of inflammatory arthritis, with an estimated prevalence of 0.1-0.9%. Genetic factors have been strongly implicated in its aetiology, and heritability as assessed by twin studies has been estimated to be >90%. HLA- B27 is almost essential for inheritance of AS; it is not merely sufficient for explaining the pattern of familial recurrence of the disease. This study's purpose is to investigate the association of ankylosing spondylitis with single-nucleotide polymorphisms (SNPs) in the IL-1 family: IL-1a (-889C/T) rs1800587, IL-1b (-511C/T) rs16944, IL-1b (+3962C/T) rs1143634, IL-1R (Pst-1 1970C/T) rs2234650 and IL-1RA (Mspa-1 11100C/T) rs315952. 99 unrelated Iranian AS patients and 217 healthy control subjects were selected. Cytokine typing was performed by the polymerase chain reaction with sequence-specific primers assay. The allele and genotype frequencies of the polymorphisms were determined: The IL1α rs1800587, IL1β rs16944 and IL1β rs1143634 were not significantly associated with AS. Genotype frequencies at IL1R rs2234650 differed between cases and controls (χ(2)=8.85; p=0.01); the IL1R rs2234650 C/T and T/T genotypes were less common in AS patients than controls. The IL1R rs2234650 C/T genotype was inversely associated with AS comparing with the IL1R rs2234650 C/C genotype (OR=0.48; p=0.005). IL1R rs2234650 C/T genotype was less common in patients than controls (OR=0.37; p=0.02).Furthermore IL1R rs2234650 T allele was strongly associated with HLA-B2702 patients rather than HLA-B2705 but was not associated with HLA-B27 negative patients (OR=0.33; p=0.01). Polymorphisms of IL1α rs1800587, IL1β rs16944 and IL1β rs1143634 were not significantly associated with ankylosing spondylitis but inversely in this study IL1R rs2234650 was significantly associated and carriage of T allele in IL1R rs2234650 seems to be protective, while carriage of C allele result in two fold higher risk of developing AS.

摘要

强直性脊柱炎(AS)是最常见的炎症性关节炎病因之一,估计患病率为 0.1-0.9%。遗传因素在其发病机制中起重要作用,双胞胎研究评估的遗传度估计超过 90%。HLA-B27 几乎是 AS 遗传的必要条件;它不仅仅足以解释疾病家族复发的模式。本研究旨在探讨强直性脊柱炎与白细胞介素-1 家族中单核苷酸多态性(SNP)的关联:白细胞介素-1a(-889C/T)rs1800587、白细胞介素-1b(-511C/T)rs16944、白细胞介素-1b(+3962C/T)rs1143634、白细胞介素-1 受体(Pst-1 1970C/T)rs2234650 和白细胞介素-1 受体拮抗剂(Mspa-1 11100C/T)rs315952。选择了 99 名伊朗强直性脊柱炎患者和 217 名健康对照者。通过聚合酶链反应与序列特异性引物检测进行细胞因子分型。确定了多态性的等位基因和基因型频率:白细胞介素 1α rs1800587、白细胞介素 1β rs16944 和白细胞介素 1β rs1143634 与 AS 无显著相关性。IL1R rs2234650 的基因型频率在病例和对照组之间存在差异(χ(2)=8.85;p=0.01);AS 患者中 IL1R rs2234650 C/T 和 T/T 基因型比对照组少见。与 IL1R rs2234650 C/C 基因型相比,IL1R rs2234650 C/T 基因型与 AS 呈负相关(OR=0.48;p=0.005)。与对照组相比,IL1R rs2234650 C/T 基因型在患者中更为少见(OR=0.37;p=0.02)。此外,IL1R rs2234650 T 等位基因与 HLA-B2702 患者而非 HLA-B2705 患者密切相关,但与 HLA-B27 阴性患者无关(OR=0.33;p=0.01)。白细胞介素 1α rs1800587、白细胞介素 1β rs16944 和白细胞介素 1β rs1143634 的多态性与强直性脊柱炎无显著相关性,但在本研究中,IL1R rs2234650 呈显著相关性,IL1R rs2234650 中的 T 等位基因似乎具有保护作用,而 C 等位基因的携带则导致患强直性脊柱炎的风险增加两倍。

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