Shirodaria S, Smith J, McKay I J, Kennett C N, Hughes F J
Department of Adult Oral Health, St Bartholomew's and the Royal London School of Medicine and Dentistry, Queen Mary and Westfield College, University of London, UK.
J Dent Res. 2000 Nov;79(11):1864-9. doi: 10.1177/00220345000790110801.
Interleukin-1 (IL-1) is a potent stimulator of bone resorption and is strongly implicated in the destruction due to bystander damage seen in periodontal disease. Recent studies suggest that polymorphisms of the (IL-1) gene complex may be significant risk factors for a number of chronic inflammatory diseases. The severity of periodontal disease has been positively associated with carriage of allele 2 at position -889 of the IL-1A gene in conjunction with allele 2 of the IL-1B gene at position +3953. In this study, we tested the hypothesis that allele 2 of the IL-1A gene at position -889 might act to elevate levels of IL-1alpha protein in patients with periodontal disease. Since levels of IL-1alpha protein are low in healthy individuals, we used a group of patients with severe periodontal disease to investigate if levels of IL-1alpha protein in gingival crevicular fluid can be correlated to patient genotype. IL-1alpha levels were measured by enzyme immunoassay in 46 patients with severe periodontal disease. These patients were genotyped by PCR and allele-specific restriction digests. The carriage rate for allele 2 in the diseased population was 68%. Overall, the carriage of allele 2 was associated with almost a four-fold increase in IL-1alpha protein levels. Differences were most pronounced in non-smokers, while heavy smokers showed reduced levels of IL-1alpha protein regardless of genotype. These results suggest a mechanism whereby this genetic polymorphism acts to modulate IL-1alpha protein production and may influence the pathogenesis of periodontal disease by affecting the extent of IL-1-associated bystander damage.
白细胞介素-1(IL-1)是骨吸收的强效刺激因子,在牙周病中因旁观者损伤导致的组织破坏中起重要作用。近期研究表明,IL-1基因复合体的多态性可能是多种慢性炎症性疾病的重要危险因素。牙周病的严重程度与IL-1A基因-889位点的2等位基因以及IL-1B基因+3953位点的2等位基因携带情况呈正相关。在本研究中,我们检验了以下假设:-889位点的IL-1A基因2等位基因可能会使牙周病患者的IL-1α蛋白水平升高。由于健康个体中IL-1α蛋白水平较低,我们使用一组重度牙周病患者来研究龈沟液中IL-1α蛋白水平是否与患者基因型相关。通过酶免疫测定法测量了46例重度牙周病患者的IL-1α水平。这些患者通过聚合酶链反应(PCR)和等位基因特异性限制性酶切进行基因分型。患病群体中2等位基因的携带率为68%。总体而言,2等位基因的携带与IL-1α蛋白水平几乎四倍的升高相关。差异在非吸烟者中最为明显,而重度吸烟者无论基因型如何,IL-1α蛋白水平均降低。这些结果提示了一种机制,即这种基因多态性通过调节IL-1α蛋白的产生来影响牙周病的发病机制,可能通过影响IL-1相关的旁观者损伤程度来实现。