Melicherčík Pavel, Klapková Eva, Kotaška Karel, Jahoda David, Landor Ivan, Čeřovský Václav
Department of Orthopaedics, First Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Úvalu 84, 150 06 Prague 5, Czech Republic.
Department of Medical Chemistry and Clinical Biochemistry, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Úvalu 84, 150 06 Prague 5, Czech Republic.
Diagnostics (Basel). 2020 Jan 9;10(1):33. doi: 10.3390/diagnostics10010033.
The α-defensins (AD) present in synovial fluid have been regarded as constituting the most accurate periprosthetic joint infection (PJI) biomarker. The methods most commonly used for estimating AD as a biomarker are the qualitative Synovasure PJI tests, based on the technique of lateral flow, and quantitative enzyme-linked immunosorbent assay (ELISA). Here, we propose a novel test based on detecting α-defensins in synovial fluid by high-performance liquid chromatography (HPLC). Synovial fluid was collected from 157 patients diagnosed with PJI, infectious arthritis (IA), arthrosis, reactive arthritis, and rheumatoid arthritis. AD concentrations in the fluid were determined by HPLC, and these same samples were used for additional diagnostic analyses. The results were statistically processed to calculate cutoff concentrations for PJI and IA. HPLC testing showed a sensitivity of 94% and a specificity of 92% for diagnosis of PJI, and a sensitivity of 97% and a specificity of 87% for diagnosis of IA. Using HPLC, we detected in synovial fluid a combination of three α-defensins: human neutrophil peptides HNP1, HNP2, and HNP3. All measured AD concentration values shown in this work refer to the sum of these three individual concentrations. Our study shows that the HPLC method meets the conditions for measuring precise concentrations of the sum of AD and can be recommended as part of a diagnostic array for PJI and IA diagnostics. By this method, we have verified that higher levels of AD in synovial fluid can also be seen in rheumatoid illnesses, crystal arthropathies, and reactive arthritis.
滑液中存在的α-防御素(AD)被认为是构成最准确的人工关节周围感染(PJI)生物标志物。最常用于将AD评估为生物标志物的方法是基于侧向流动技术的定性Synovasure PJI检测和定量酶联免疫吸附测定(ELISA)。在此,我们提出一种基于高效液相色谱(HPLC)检测滑液中α-防御素的新型检测方法。从157例被诊断为PJI、感染性关节炎(IA)、关节病、反应性关节炎和类风湿性关节炎的患者中收集滑液。通过HPLC测定滑液中的AD浓度,并将这些相同的样本用于其他诊断分析。对结果进行统计学处理以计算PJI和IA的临界浓度。HPLC检测显示诊断PJI的灵敏度为94%,特异性为92%,诊断IA的灵敏度为97%,特异性为87%。使用HPLC,我们在滑液中检测到三种α-防御素的组合:人中性粒细胞肽HNP1、HNP2和HNP3。本研究中所示的所有测量AD浓度值均指这三种单独浓度的总和。我们的研究表明,HPLC方法满足测量AD总和精确浓度的条件,可推荐作为PJI和IA诊断诊断阵列的一部分。通过这种方法,我们已经证实,在类风湿性疾病、结晶性关节病和反应性关节炎中也可以看到滑液中AD水平较高。