Cipriano Cara, Maiti Aparna, Hale Gregory, Jiranek William
Department of Orthopaedic Surgery, Virginia Commonwealth University, 1112 East Clay Street, McGuire Hall Annex, Richmond, VA 23298. E-mail address for C. Cipriano:
J Bone Joint Surg Am. 2014 Oct 15;96(20):1692-8. doi: 10.2106/JBJS.M.01295.
Toll-like receptors (TLRs) 1 and 6 are consistent molecular indicators of the host inflammatory response against bacterial infection. Our aims were to determine whether TLR elevation could be detected in infected periprosthetic tissues and to assess the utility of these biomarkers as tests for detecting a periprosthetic joint infection.
Fifty-nine patients undergoing revision total joint arthroplasty (twenty-seven hips and thirty-two knees) were prospectively evaluated for periprosthetic joint infection according to currently recommended diagnostic criteria. Nine patients were excluded because of insufficient work-up, leaving fifty available for study. Of these, twenty-one were categorized as infected and twenty-nine as noninfected. Periprosthetic tissues were collected intraoperatively, and total RNA was extracted by standard techniques. Expression of TLR messenger RNAs was assessed by first-strand complementary DNA synthesis from 1 μg of total RNA followed by real-time PCR (polymerase chain reaction). Results were normalized relative to the housekeeping gene GAPDH (glyceraldehyde 3-phosphate dehydrogenase). Expression of TLRs 1, 6, and 10 in the infected and noninfected groups was compared with use of the Student t test. The receiver operating characteristic curve, area under the curve (AUC), sensitivity, specificity, positive likelihood ratio (LR+), and negative likelihood ratio (LR-) were calculated to determine the accuracy of each TLR for predicting periprosthetic joint infection at its optimal diagnostic threshold.
Mean TLR1 mRNA expression was significantly elevated in infected compared with noninfected samples (0.600 compared with 0.005, p = 0.0003); the same was true of TLR6 (0.208 compared with 0.0165, p = 0.0059) but not of TLR10 (0.00019 compared with 0.00014, p = 0.6238). The AUC was 0.995 for TLR1, 0.883 for TLR6, and 0.546 for TLR10. The optimal threshold for diagnosing periprosthetic joint infection was 0.0924 for TLR1 (sensitivity = 95.2%, specificity = 100%, LR+ = 13.80, LR- = 0.91) and 0.0215 for TLR6 (sensitivity = 85.7%, specificity = 82.8%, LR+ = 4.98, LR- = 0.83).
In our pilot study, TLR1 expression in periprosthetic tissues most accurately predicted periprosthetic joint infection. This measure of the host response may be particularly helpful in detecting culture-negative infections and avoiding false positives resulting from contamination.
Diagnostic Level III. See Instructions for Authors for a complete description of levels of evidence.
Toll样受体(TLR)1和6是宿主针对细菌感染的炎症反应的一致性分子指标。我们的目的是确定在感染的假体周围组织中是否能检测到TLR升高,并评估这些生物标志物作为检测假体周围关节感染的测试方法的效用。
根据目前推荐的诊断标准,对59例行翻修全关节置换术的患者(27例髋关节和32例膝关节)进行前瞻性评估,以确定是否存在假体周围关节感染。9例患者因检查不充分被排除,剩余50例可供研究。其中,21例被归类为感染,29例为未感染。术中收集假体周围组织,采用标准技术提取总RNA。通过从1μg总RNA进行第一链互补DNA合成,随后进行实时聚合酶链反应(PCR)来评估TLR信使RNA的表达。结果相对于管家基因甘油醛-3-磷酸脱氢酶(GAPDH)进行标准化。使用Student t检验比较感染组和未感染组中TLR1、6和10的表达。计算受试者工作特征曲线、曲线下面积(AUC)、敏感性、特异性、阳性似然比(LR+)和阴性似然比(LR-),以确定每个TLR在其最佳诊断阈值下预测假体周围关节感染的准确性。
与未感染样本相比,感染样本中TLR1信使RNA的平均表达显著升高(分别为0.600和0.005,p = 0.0003);TLR6也是如此(分别为0.208和0.0165,p = 0.0059),但TLR10并非如此(分别为0.00019和0.00014,p = 0.6238)。TLR1的AUC为0.995,TLR6为0.883,TLR10为0.546。诊断假体周围关节感染的最佳阈值,TLR1为0.0924(敏感性 = 95.2%,特异性 = 100%,LR+ = 13.80,LR- = 0.91),TLR6为0.0215(敏感性 = 85.7%,特异性 = 82.8%,LR+ = 4.98,LR- = 循环冗余校验)。
在我们的初步研究中,假体周围组织中TLR1的表达最准确地预测了假体周围关节感染。这种宿主反应的测量方法可能对检测培养阴性感染以及避免因污染导致的假阳性特别有帮助。
诊断性III级。有关证据水平的完整描述,请参阅作者须知。