Fillerova Regina, Gallo Jiri, Radvansky Martin, Kraiczova Veronika, Kudelka Milos, Kriegova Eva
Department of Immunology, Faculty of Medicine and Dentistry, Palacky University & University Hospital, Olomouc, Czech Republic.
Deptartment of Orthopaedics, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
J Clin Microbiol. 2017 Sep;55(9):2686-2697. doi: 10.1128/JCM.00558-17. Epub 2017 Jun 21.
The timely and exact diagnosis of prosthetic joint infection (PJI) is crucial for surgical decision-making. Intraoperatively, delivery of the result within an hour is required. Alpha-defensin lateral immunoassay of joint fluid (JF) is precise for the intraoperative exclusion of PJI; however, for patients with a limited amount of JF and/or in cases where the JF is bloody, this test is unhelpful. Important information is hidden in periprosthetic tissues that may much better reflect the current status of implant pathology. We therefore investigated the utility of the gene expression patterns of 12 candidate genes (, -, -, -, and , , , , , , , and ) previously associated with infection for detection of PJI in periprosthetic tissues of patients with total joint arthroplasty (TJA) ( = 76) reoperated for PJI ( = 38) or aseptic failure ( = 38), using the ultrafast quantitative reverse transcription-PCR (RT-PCR) Xxpress system (BJS Biotechnologies Ltd.). Advanced data-mining algorithms were applied for data analysis. For PJI, we detected elevated mRNA expression levels of ( < 0.0001), ( < 0.0001), ( < 0.0001), ( = 0.02), and ( = 0.01) in comparison to those in tissues from aseptic cases. A feature selection algorithm revealed that the pattern was the most appropriate for detection/exclusion of PJI, achieving 94.5% sensitivity and 95.7% specificity, with likelihood ratios (LRs) for positive and negative results of 16.3 and 0.06, respectively. Taken together, the results show that gene expression detection by use of ultrafast qRT-PCR linked to an electronic calculator allows detection of patients with a high probability of PJI within 45 min after sampling. Further testing on a larger cohort of patients is needed.
人工关节感染(PJI)的及时准确诊断对于手术决策至关重要。术中需要在一小时内给出检测结果。关节液(JF)的α-防御素侧向免疫测定对于术中排除PJI很精确;然而,对于JF量有限的患者和/或JF为血性的情况,该检测毫无帮助。重要信息隐藏在假体周围组织中,这些组织可能能更好地反映植入物病理的当前状态。因此,我们使用超快定量逆转录聚合酶链反应(RT-PCR)Xxpress系统(BJS生物技术有限公司),研究了先前与感染相关的12个候选基因(, - , - , - ,以及 , , , , , , , )的基因表达模式在接受全关节置换术(TJA)( = 76)后因PJI( = 38)或无菌性失败( = 38)而再次手术的患者的假体周围组织中检测PJI的效用。应用先进的数据挖掘算法进行数据分析。与无菌病例的组织相比,对于PJI,我们检测到 ( < 0.0001)、 ( < 0.0001)、 ( < 0.0001)、 ( = 0.02)和 ( = 0.01)的mRNA表达水平升高。一种特征选择算法显示, 模式最适合检测/排除PJI,灵敏度达到94.5%,特异性达到95.7%,阳性和阴性结果的似然比(LRs)分别为16.3和0.06。综上所述,结果表明,通过使用与电子计算器相连的超快qRT-PCR进行 基因表达检测,能够在采样后45分钟内检测出极有可能患有PJI的患者。需要在更大规模的患者队列中进行进一步测试。