首页> 外文OA文献 >Genetska podloga aseptičke nestabilnosti totalne endoproteze zgloba kuka Genetic background of aseptic instability after total hip arthroplasty.
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Genetska podloga aseptičke nestabilnosti totalne endoproteze zgloba kuka Genetic background of aseptic instability after total hip arthroplasty.

机译:全髋关节置内假体无菌性不稳定的遗传背景全髋关节置换术后无菌性不稳定的遗传背景。

摘要

Total hip arthroplasty (THA) has dramatically improved the treatment of an entire range of hip joint diseases. On the other hand, however, it has favored the development of a new disease - periprosthetic osteolysis with a consequent instability of THA. Aseptic instability is the major late complication of THA and the main reason of its malfunction. Molecular and cellular mechanisms of this complication have been thoroughly studied. The importance of prosthetic materials and design have been clearly demonstrated. However, existence of individual susceptibility to development of this complication that is determined neither by endoprothesis properties nor by demographic or morbidity characteristics of a patient has also been recognized. In the recent years, several smaller studies have tried to define the "genetic background of the individual susceptibility" towards the development of aseptic instability. All these studies followed the same logic - they searched for a link between the complication and genes coding for mediators of inflammation and/or bone remodeling, particularly those with known polymorphisms that influence expression/activity. Several associations have been found indicating, at least theoretically, a potential of developing a system of relatively reliable individual risk prediction, which in turn could result in individualized choice of prosthetic material, postoperative therapy programs and medication therapy. However, this research is at an early stage and future efforts should be focused on a) identification of genetic markers - reliable predictors and b) identification of functional links between particular genetic markers and aseptic instability. It is impossible to meet these goals without application of techniques of proteomic analysis.
机译:全髋关节置换术(THA)大大改善了整个髋关节疾病的治疗范围。但是,另一方面,它有利于发展一种新的疾病-假体周围骨溶解,从而导致THA不稳定。无菌不稳定是THA的主要晚期并发症,也是THA故障的主要原因。已经对这种并发症的分子和细胞机制进行了深入研究。假体材料和设计的重要性已得到明确证明。然而,也已经认识到个体对这种并发症发展的易感性,既不由内用假体的性质也不由患者的人口统计学或发病率特征决定。近年来,几项较小的研究试图为无菌不稳定性的发展定义“个体易感性的遗传背景”。所有这些研究都遵循相同的逻辑-他们在并发症和编码炎症和/或骨骼重塑介体的基因之间寻找联系,特别是那些具有已知多态性的基因会影响表达/活性。已经发现一些协会,至少在理论上表明有发展相对可靠的个人风险预测系统的潜力,这反过来又可能导致假体材料,术后治疗方案和药物治疗的个性化选择。但是,这项研究仍处于早期阶段,未来的工作应集中在a)遗传标记的鉴定-可靠的预测因子和b)特定遗传标记与无菌不稳定性之间的功能联系上。如果不应用蛋白质组学分析技术,就不可能实现这些目标。

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