Ásta Dögg Jónasdóttir, Peter Hemmingsson, Angelina Schwarz, Magnus Söderberg, Annika Wernerson, Abdul Rashid Qureshi, Aleksandra Antovic, Iva Gunnarsson, Annette Bruchfeld
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Kidney biopsies from AAV patients were stained for TWEAK and its receptor fibroblast growth factor-inducible 14 (Fn14) using immunohistochemistry (IHC).</p><p><strong>Results: </strong>sTWEAK was measured in 74 patients and uTWEAK in 69 patients, 42 of whom had kidney involvement. uTWEAK-to-creatinine ratio (uTWEAK/Cr) was significantly higher at baseline compared with follow-up (median 7.21 vs 4.94 ng/mmol, <i>P</i> < .0001). Patients with kidney involvement had higher uTWEAK/Cr levels compared with those without (<i>P</i> = .03). A correlation was found between uTWEAK/Cr and BVAS (<i>P</i> = .006), albuminuria (<i>P</i> = .022) and crescentic changes (<i>P</i> = .03). sTWEAK levels were higher in patients at inclusion than at follow-up (<i>P</i> = .009) but no difference was found when comparing patients and controls, nor did sTWEAK correlate with BVAS. IHC staining showed a clear expression of TWEAK but a fainter pattern of Fn14 in kidney biopsies from AAV patients.</p><p><strong>Conclusions: </strong>uTWEAK/Cr correlated with BVAS, albuminuria and number of crescents in active AAV and may be a useful biomarker in assessing disease activity in patients with AAV, whereas sTWEAK level is not.</p>","PeriodicalId":10435,"journal":{"name":"Clinical Kidney Journal","volume":"18 5","pages":"sfaf086"},"PeriodicalIF":4.6000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12121554/pdf/","citationCount":"0","resultStr":"{\"title\":\"Urinary TWEAK reflects disease activity in ANCA-associated vasculitis.\",\"authors\":\"Ásta Dögg Jónasdóttir, Peter Hemmingsson, Angelina Schwarz, Magnus Söderberg, Annika Wernerson, Abdul Rashid Qureshi, Aleksandra Antovic, Iva Gunnarsson, Annette Bruchfeld\",\"doi\":\"10.1093/ckj/sfaf086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The aim of the study was to investigate urinary and serum tumour necrosis factor (TNF)-like weak inducer of apoptosis (TWEAK) as potential biomarkers in a longitudinal cohort of patients with ANCA-associated vasculitis (AAV).</p><p><strong>Methods: </strong>Patients with active AAV were included in the study. The Birmingham Vasculitis Score 2003 (BVAS) was used for assessment of disease activity and C-reactive protein (CRP), creatinine, albuminuria, and serum (s) and urinary (u) TWEAK levels were measured at baseline and 6-month follow-up. sTWEAK was measured in population-based controls for comparison. Kidney biopsies from AAV patients were stained for TWEAK and its receptor fibroblast growth factor-inducible 14 (Fn14) using immunohistochemistry (IHC).</p><p><strong>Results: </strong>sTWEAK was measured in 74 patients and uTWEAK in 69 patients, 42 of whom had kidney involvement. uTWEAK-to-creatinine ratio (uTWEAK/Cr) was significantly higher at baseline compared with follow-up (median 7.21 vs 4.94 ng/mmol, <i>P</i> < .0001). Patients with kidney involvement had higher uTWEAK/Cr levels compared with those without (<i>P</i> = .03). 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引用次数: 0
摘要
背景:该研究的目的是研究尿液和血清肿瘤坏死因子(TNF)样细胞凋亡弱诱导剂(TWEAK)作为anca相关性血管炎(AAV)患者纵向队列中的潜在生物标志物。方法:选取活动性AAV患者作为研究对象。2003年伯明翰血管炎评分(BVAS)用于评估疾病活动性,并在基线和6个月随访时测量c反应蛋白(CRP)、肌酐、蛋白尿、血清和尿TWEAK水平。在以人群为基础的对照中测量sTWEAK进行比较。采用免疫组化(IHC)方法对AAV患者肾活检进行TWEAK及其受体成纤维细胞生长因子诱导14 (Fn14)染色。结果:74例患者测量了sTWEAK, 69例患者测量了uTWEAK,其中42例患者有肾脏受累。基线时uTWEAK/肌酐比值(uTWEAK/Cr)显著高于随访时(中位值7.21 vs 4.94 ng/mmol, P < 0.0001)。肾脏受累患者的uTWEAK/Cr水平高于未受累患者(P = .03)。uTWEAK/Cr与BVAS (P = 0.006)、蛋白尿(P = 0.022)和新月形变化(P = 0.03)存在相关性。纳入时患者的sTWEAK水平高于随访时(P = 0.009),但在比较患者和对照组时没有发现差异,sTWEAK也与BVAS无关。在AAV患者的肾活检中,免疫组化染色显示明显的TWEAK表达,但Fn14的表达较弱。结论:uTWEAK/Cr与活动性AAV患者的BVAS、蛋白尿和新月数相关,可能是评估AAV患者疾病活动性的有用生物标志物,而sTWEAK水平则不是。
Urinary TWEAK reflects disease activity in ANCA-associated vasculitis.
Background: The aim of the study was to investigate urinary and serum tumour necrosis factor (TNF)-like weak inducer of apoptosis (TWEAK) as potential biomarkers in a longitudinal cohort of patients with ANCA-associated vasculitis (AAV).
Methods: Patients with active AAV were included in the study. The Birmingham Vasculitis Score 2003 (BVAS) was used for assessment of disease activity and C-reactive protein (CRP), creatinine, albuminuria, and serum (s) and urinary (u) TWEAK levels were measured at baseline and 6-month follow-up. sTWEAK was measured in population-based controls for comparison. Kidney biopsies from AAV patients were stained for TWEAK and its receptor fibroblast growth factor-inducible 14 (Fn14) using immunohistochemistry (IHC).
Results: sTWEAK was measured in 74 patients and uTWEAK in 69 patients, 42 of whom had kidney involvement. uTWEAK-to-creatinine ratio (uTWEAK/Cr) was significantly higher at baseline compared with follow-up (median 7.21 vs 4.94 ng/mmol, P < .0001). Patients with kidney involvement had higher uTWEAK/Cr levels compared with those without (P = .03). A correlation was found between uTWEAK/Cr and BVAS (P = .006), albuminuria (P = .022) and crescentic changes (P = .03). sTWEAK levels were higher in patients at inclusion than at follow-up (P = .009) but no difference was found when comparing patients and controls, nor did sTWEAK correlate with BVAS. IHC staining showed a clear expression of TWEAK but a fainter pattern of Fn14 in kidney biopsies from AAV patients.
Conclusions: uTWEAK/Cr correlated with BVAS, albuminuria and number of crescents in active AAV and may be a useful biomarker in assessing disease activity in patients with AAV, whereas sTWEAK level is not.
期刊介绍:
About the Journal
Clinical Kidney Journal: Clinical and Translational Nephrology (ckj), an official journal of the ERA-EDTA (European Renal Association-European Dialysis and Transplant Association), is a fully open access, online only journal publishing bimonthly. The journal is an essential educational and training resource integrating clinical, translational and educational research into clinical practice. ckj aims to contribute to a translational research culture among nephrologists and kidney pathologists that helps close the gap between basic researchers and practicing clinicians and promote sorely needed innovation in the Nephrology field. All research articles in this journal have undergone peer review.