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Association of macrophage migration inhibitory factor gene polymorphisms with chronic periodontitis in a South Eastern Iranian population

机译:伊朗东南部人群巨噬细胞迁移抑制因子基因多态性与慢性牙周炎的关系

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Background: Macrophage migration inhibitory factor (MIF) is a key proinflammatory mediator. It plays a vital role in immune response against the oral disease. MIF is a regulator of innate immunity, and bacterial antigens can stimulate serum level of this protein. In experimental gingivitis, the expression level of MIF increases and this increment positively correlates with oral plaque index. The single nucleotide polymorphisms in the gene encoding the MIF protein can control the function of MIF. The aim of the present study was a clarification of the associations between MIF?173 G/C, MIF 95 bp, and 189 bp insertion/deletion (I/D) polymorphisms and chronic periodontitis (CP) compared with healthy controls. Materials and Methods: This case–control study was carried out on 210 CP patients and 100 normal subjects. MIF?173 G/C and MIF 95 bp and 189 bp I/D polymorphisms were genotyped, using polymerase chain reaction–restriction fragment-length polymorphism (PCR-RFLP) and PCR, respectively. Allele and genotype frequencies of the variants were compared between patients and controls using Chi?square. test. The value of P < 0.05 was considered statistically significant. Results: The study findings showed that MIF?173 G/C polymorphism, especially the C allele increased the risk of CP. The 95?bp I/D polymorphism was not associated with CP and the 185?bp I/D variant was not polymorphic in our population. Conclusion: Therefore, MIF?137 G/C variant increased the risk of CP in the South East of the Iranian population. In other words, polymorphisms in MIF gene influence clinical outcome of CP infection and influence the susceptibility to disease. Further studies with larger sample sizes and different ethnicities are required to validate our findings. Key Words: Chronic periodontitis, gene, Macrophage Migration-Inhibitory Factors, migration inhibitory factor, polymorphism
机译:背景:巨噬细胞迁移抑制因子(MIF)是关键的促炎介质。它在针对口腔疾病的免疫反应中起着至关重要的作用。 MIF是先天免疫的调节剂,细菌抗原可以刺激该蛋白的血清水平。在实验性牙龈炎中,MIF的表达水平增加,并且这种增加与口腔菌斑指数呈正相关。编码MIF蛋白的基因中的单核苷酸多态性可以控制MIF的功能。本研究的目的是弄清MIF?173 G / C,MIF 95 bp和189 bp插入/缺失(I / D)多态性与慢性牙周炎(CP)之间的关联。材料和方法:本病例对照研究是针对210名CP患者和100名正常受试者进行的。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和PCR分别对MIF?173 G / C和MIF 95 bp和189 bp I / D多态性进行基因分型。使用卡方检验比较了患者和对照组之间变异的等位基因和基因型频率。测试。 P <0.05的值被认为具有统计学意义。结果:研究结果表明MIF?173 G / C多态性,特别是C等位基因增加了CP的风险。 95 bp I / D多态性与CP无关,而185 bp I / D变异体在我们的人群中也不具有多态性。结论:因此,MIF?137 G / C变异体增加了伊朗人口东南部CP的风险。换句话说,MIF基因的多态性会影响CP感染的临床结果并影响疾病的易感性。需要进行更大样本量和不同种族的进一步研究,以验证我们的发现。关键词:慢性牙周炎;基因;巨噬细胞迁移抑制因子;迁移抑制因子;多态性

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