Xie Lin, Li Wei, Ye Wei-Ming, Xiao Yao, Ke Wu-Jian, Niu Jian-Jun, Yang Tian-Ci
Center of Clinical Laboratory, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Department of Hospital Infection Management, School of Medicine, Zhongshan Hospital of Xiamen University, Xiamen University, Xiamen, China.
Clin Infect Dis. 2023 Aug 14;77(3):472-479. doi: 10.1093/cid/ciad158.
Laboratory tests to diagnose neurosyphilis using cerebrospinal fluid (CSF) are currently disadvantageous as a lumbar puncture is required, which may result in patients with neurosyphilis missing an opportunity for early diagnosis. Thus, blood biomarker candidates that are more convenient and minimally invasive to collect for diagnosing neurosyphilis is urgently needed.
This observational study aimed to analyze serum ubiquitin C-terminal hydrolase-L1 (UCH-L1), glial fibrillary acidic protein (GFAP), and neurofilament light chain (NF-L) levels in 153 patients without human immunodeficiency virus (HIV) and to evaluate their diagnostic performance in neurosyphilis compared with CSF.
Serum UCH-L1, GFAP, and NF-L levels were significantly higher in patients with neurosyphilis compared with patients with uncomplicated syphilis or non-syphilis. For the diagnosis of neurosyphilis, serum UCH-L1, GFAP, and NF-L revealed sensitivities of 90.20%, 80.40%, and 88.24%, and specificities of 92.16%, 78.43%, and 80.39%, respectively, at cutoff levels of 814.50 pg/mL, 442.70 pg/mL, and 45.19 pg/mL, respectively. In patients with syphilis, serum UCH-L1, GFAP, and NF-L levels correlated strongly or moderately with those in the CSF, with similar or better diagnostic performance than those in the CSF. The testing algorithms' sensitivity and specificity increased to 98.04% and 96.08%, respectively, when subjected to parallel and combination testing, respectively.
To avoid lumbar puncture, each serum UCH-L1, GFAP, and NF-L is a good entry point and biomarker candidate for the diagnosis of neurosyphilis among patients without HIV. These proteins used in concerto can further improve the diagnostic sensitivity and specificity.
目前,使用脑脊液(CSF)诊断神经梅毒的实验室检测存在劣势,因为需要进行腰椎穿刺,这可能导致神经梅毒患者错过早期诊断的机会。因此,迫切需要更方便且微创的血液生物标志物候选物来诊断神经梅毒。
这项观察性研究旨在分析153例无人类免疫缺陷病毒(HIV)患者的血清泛素C末端水解酶-L1(UCH-L1)、胶质纤维酸性蛋白(GFAP)和神经丝轻链(NF-L)水平,并与脑脊液相比评估它们在神经梅毒中的诊断性能。
与单纯梅毒或非梅毒患者相比,神经梅毒患者的血清UCH-L1、GFAP和NF-L水平显著更高。对于神经梅毒的诊断,血清UCH-L1、GFAP和NF-L在截断水平分别为814.50 pg/mL、442.70 pg/mL和45.19 pg/mL时,敏感性分别为90.20%、80.40%和88.24%,特异性分别为92.16%、78.43%和80.39%。在梅毒患者中,血清UCH-L1、GFAP和NF-L水平与脑脊液中的水平强烈或中度相关,诊断性能与脑脊液相似或更好。当进行平行和联合检测时,检测算法的敏感性和特异性分别提高到98.04%和96.08%。
为避免腰椎穿刺,血清UCH-L1、GFAP和NF-L中的每一种都是诊断无HIV患者神经梅毒的良好切入点和生物标志物候选物。这些蛋白联合使用可进一步提高诊断敏感性和特异性。