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Predictive Role of Cytokine Gene Polymorphisms for the Development of Femoral Head Osteonecrosis

机译:细胞因子基因多态性在股骨头坏死发展中的预测作用。

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摘要

Introduction: Osteonecrosis (ON) is a multifactorial disease that leads to hip destruction. Lately, much focus has been at femoral head preservation with nonsurgical methods. In this study we examined the polymorphisms of IL-1α, IL-1R, IL-1RA, IL-4Rα, IL-1β, IL-12, γIFN, TGF-β, TNF-a, IL-2, IL-4, IL-6 and IL-10 genes for evaluation of their contribution in ON. Material and methods: DNA was extracted from 112 ON patients and 438 healthy donors. Analysis of the polymorphisms was completed using the PCR-SSP method. Statistical analysis was performed using the χ2 test to compare the genotype and allelic frequency distribution. Results: The CT and GA genotypes of the IL-1α (-889) and TNF-a (-238) genes were found higher in the patients (51.8% and 10.8%, respectively) compared to the healthy donors (39.7% and 2.1%, respectively). In TGF-β codon 25, the G to C polymorphism in the homozygous state was found in 1.8% of the patients and the C allele frequency was 8.9%, whereas the G allele frequency was 91.1%. Also, at the IL-10 (-1082) gene the GG genotype was 16.2% in the controls whereas in the patients was 7.2%. Conclusions: Based on the above, we showed that certain genotypes of the IL-1α, TGF-β, IL-10 and TNF-a genes could be related in the pathogenesis of a complicated disease, such as osteonecrosis. The presence of one of the above mentioned polymorphisms or the simultaneous carriage of more than one may further increase the risk for osteonecrosis, especially in those at high risk, such as patients receiving corticosteroids.
机译:简介:骨坏死(ON)是导致髋关节破坏的多因素疾病。近来,许多焦点集中在用非手术方法保存股骨头上。在这项研究中,我们研究了IL-1α,IL-1R,IL-1RA,IL-4Rα,IL-1β,IL-12,γIFN,TGF-β,TNF-α,IL-2,IL-4的多态性, IL-6和IL-10基因,用于评估它们在ON中的作用。材料和方法:从112位ON患者和438位健康供体中提取DNA。使用PCR-SSP方法完成了多态性分析。使用χ 2 检验进行统计分析,以比较基因型和等位基因频率分布。结果:与健康供体(分别为39.7%和2.1)相比,患者中IL-1α(-889)和TNF-a(-238)基因的CT和GA基因型更高(分别为51.8%和10.8%)。 %, 分别)。在TGF-β密码子25中,在1.8%的患者中发现纯合状态的G至C多态性,C等位基因频率为8.9%,而G等位基因频率为91.1%。同样,在IL-10(-1082)基因上,对照组的GG基因型为16.2%,而患者为7.2%。结论:基于以上所述,我们表明IL-1α,TGF-β,IL-10和TNF-a基因的某些基因型可能与诸如骨坏死等复杂疾病的发病机制有关。上述多态性之一的存在或同时携带一种以上可能会进一步增加骨坏死的风险,尤其是在那些高风险人群中,例如接受皮质类固醇的患者。

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