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白细胞介素-1 基因座多态性与动脉粥样硬化和主动脉瘤血管疾病患者的慢性牙周炎。

Polymorphisms in the interleukin-1 gene locus and chronic periodontitis in patients with atherosclerotic and aortic aneurysmal vascular diseases.

机构信息

Department of Oral Biology, Faculty of Dentistry, University of Oslo, Oslo, Norway.

出版信息

Scand J Immunol. 2014 May;79(5):338-45. doi: 10.1111/sji.12166.

DOI:10.1111/sji.12166
PMID:24612355
Abstract

Chronic periodontitis (CP) and atherosclerotic and aortic aneurysmal vascular diseases (VD) are inflammatory conditions that share a number of predisposing factors. They have a complex genetic heritability and may share genetic risk factors, but a well-defined relationship is still not determined. In addition, distinct genetic patterns of predisposition have been associated with these diseases. Here, we investigated the association of polymorphisms in the IL-1 gene locus with CP in a case-case study analysing VD patients with or without CP. Seventy-four patients with VD of whom 36 had CP were genotyped for single nucleotide polymorphisms in the IL1A -889 (rs1800587), IL1B +3954 (rs1143634) and IL1B at -511 (rs16944) genes and for VNTR polymorphisms in the IL1RN gene. A significantly higher frequency (17%) for allele 1 (four repeats) of the IL1RN VNTR gene was found among the VD patients with CP compared to those without CP. In addition, the frequency of the IL1RN VNTR genotypes 1/1 (4/4 repeats) and 2/2 (2/2 repeats) were significantly higher and lower, respectively, in VD patients with CP. These findings suggest an association of genetic polymorphisms in the IL1-gene locus with risk for CP in patients with VD. The carriage of the risk genotypes, the development and the subsequent influence of CP on systemic health may constitute an additional burden in the pathogenesis of VD. This emphasizes the importance of effective periodontal treatment in patients with VD.

摘要

慢性牙周炎(CP)和动脉粥样硬化性及主动脉瘤性血管疾病(VD)是具有共同诱发因素的炎症性疾病。它们具有复杂的遗传遗传性,可能具有共同的遗传风险因素,但尚未确定明确的关系。此外,与这些疾病相关的具有独特遗传倾向性的基因模式也已被确定。在此,我们通过分析患有或不患有 CP 的 VD 患者的病例对照研究,调查了 IL-1 基因座多态性与 CP 的相关性。对 74 名 VD 患者(其中 36 名患有 CP)进行了 IL1A-889(rs1800587)、IL1B+3954(rs1143634)和 IL1B-511(rs16944)基因的单核苷酸多态性以及 IL1RN 基因中的 VNTR 多态性的基因分型。在患有 CP 的 VD 患者中,IL1RN VNTR 基因的等位基因 1(4 个重复)的频率(17%)显著高于不患有 CP 的患者。此外,IL1RN VNTR 基因型 1/1(4/4 个重复)和 2/2(2/2 个重复)的频率在患有 CP 的 VD 患者中分别显著更高和更低。这些发现提示 IL1 基因座中的遗传多态性与 VD 患者的 CP 风险相关。携带风险基因型、CP 的发展以及随后对全身健康的影响可能在 VD 的发病机制中构成额外的负担。这强调了在 VD 患者中进行有效牙周治疗的重要性。

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