Department of Biochemistry, Faculty of Science, Ain Shams University, Cairo, Egypt.
Department of Internal Medicine and Rheumatology, Faculty of Medicine, Tanta University, Tanta, Egypt.
Saudi J Kidney Dis Transpl. 2021 Jan-Feb;32(1):19-29. doi: 10.4103/1319-2442.318522.
There is no single biomarker to detect lupus nephritis (LN) activity. Renal biopsy is still the gold standard method but it is invasive and mainly used in the initial assessment of the patients. Urinary tumor necrosis factor-like weak inducer of apoptosis (uTWEAK) and urinary monocyte chemo-attractant protein-1 (uMCP-1) can be secreted in the urine of active LN. The aim of the study is to assess the potential role of uTWEAK and uMCP-1 in lupus patients and to determine their correlation with disease activity. This is a case-control study conducted on a total of 114 subjects; 92 systemic lupus erythematosus (SLE) patients and 22 healthy volunteers. The patients were recruited from the rheumatology unit at the internal medicine department, Tanta University Hospital, Tanta, Egypt. The patients and controls were subjected to full history taking, complete clinical examination, routine laboratory tests, uTWEAK and uMCP-1 measurement, assessment of the disease activity using SLE Disease Activity Index (SLEDAI), and renal SLEDAI (rSLEDAI) scores. uTWEAK and uMCP-1 levels were higher in SLE with active nephritis group than those of other SLE groups and controls. There was a significant positive correlation between uTWEAK and uMCP-1 levels in lupus patients with proteinuria, anti-dsDNA, SLEDAI and r-SLEDAI and a negative correlation with C3 and C4. TWEAK showed a sensitivity of 80.43% and 100% and specificity of 50% and 100% in detecting lupus activity and LN activity, respectively. Furthermore, uMCP-1 showed a sensitivity of 82.6% and 100% and specificity of 50% and 100% in detecting lupus activity and LN activity, respectively. uTWEAK and uMCP-1 are new, easily obtained, accurate markers with high sensitivity and specificity in the detection of LN activity.
尚无单一的生物标志物可用于检测狼疮肾炎(LN)活动度。肾活检仍然是金标准方法,但它具有侵袭性,主要用于患者的初始评估。尿肿瘤坏死因子样弱凋亡诱导剂(uTWEAK)和尿单核细胞趋化蛋白-1(uMCP-1)可在活动期 LN 患者的尿液中分泌。本研究旨在评估 uTWEAK 和 uMCP-1 在狼疮患者中的潜在作用,并确定它们与疾病活动度的相关性。这是一项总共纳入 114 例受试者的病例对照研究;92 例系统性红斑狼疮(SLE)患者和 22 例健康志愿者。这些患者是从埃及坦塔大学医院内科风湿病科招募的。对患者和对照者进行详细的病史采集、全面的临床检查、常规实验室检查、uTWEAK 和 uMCP-1 测量、使用系统性红斑狼疮疾病活动指数(SLEDAI)和肾脏 SLEDAI(rSLEDAI)评分评估疾病活动度。SLE 伴活动性肾炎组的 uTWEAK 和 uMCP-1 水平高于其他 SLE 组和对照组。狼疮患者蛋白尿、抗 dsDNA、SLEDAI 和 r-SLEDAI 与 uTWEAK 和 uMCP-1 水平呈显著正相关,与 C3 和 C4 呈负相关。TWEAK 在检测狼疮活动度和 LN 活动度方面的敏感性分别为 80.43%和 100%,特异性分别为 50%和 100%。此外,uMCP-1 在检测狼疮活动度和 LN 活动度方面的敏感性分别为 82.6%和 100%,特异性分别为 50%和 100%。uTWEAK 和 uMCP-1 是新型、易于获得的、具有高灵敏度和特异性的准确标志物,可用于检测 LN 活动度。