Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/207276
Title: Combining neutrophil and macrophage biomarkers to detect active disease in ANCA vasculitis: a combinatory model of calprotectin and urine CD163.
Author: Anton Pampols, Paula
Martínez Valenzuela, Laura
Fernandez Lorente, Loreto
Quero Ramos, Maria
Gómez Preciado, Francisco
Martín Capón, Irene
Morandeira-Rego, Francisco
Manrique Escola, Joaquín
Fulladosa, Xavier
Cruzado, Josep Ma.
Torras Ambròs, Joan
Draibe, Juliana
Keywords: Vasculitis
Marcadors bioquímics
Diagnòstic
Vasculitis
Biochemical markers
Diagnosis
Issue Date: 7-Dec-2022
Publisher: Oxford University Press
Abstract: Background: CD163 and calprotectin have been proposed as biomarkers of active renal vasculitis. This study aimed to determine whether the combination of serum/urine calprotectin (s/uCalprotectin) and urinary soluble CD163 (suCD163) increases their individual performance as activity biomarkers. Methods: We included 138 patients diagnosed with ANCA vasculitis (n = 52 diagnostic phase, n = 86 remission). The study population was divided into the inception (n = 101) and the validation cohorts (n = 37). We determined the s/uCalprotectin and suCD163 concentration using enzyme-linked immunoassay at the diagnostic or at the remission phase. Receiver operating characteristic (ROC) curves were conducted to assess the biomarkers' classificatory values. We elaborated a combinatorial biomarker model in the inception cohort. The ideal cutoffs were used in the validation cohort to confirm the model's accuracy in the distinction between active disease and remission. We added the classical ANCA vasculitis activity biomarkers to the model to increase the classificatory performance. Results: The concentrations of sCalprotectin and suCD163 were higher in the diagnostic compared with the remission phase (P = .013 and P < .0001). According to the ROC curves, sCalprotectin and suCD163 were accurate biomarkers to discern activity [area under the curve 0.73 (0.59-0.86), P = .015 and 0.88 (0.79-0.97), P < .0001]. The combinatory model with the best performance in terms of sensitivity, specificity and likelihood ratio included sCalprotectin, suCD163 and haematuria. Regarding the inception and the validation cohort, we obtained a sensitivity, specificity and likelihood ratio of 97%, 90% and 9.7, and 78%, 94% and 13, respectively. Conclusions: In patients with ANCA vasculitis, a predictive model combining sCalprotectin, suCD163 and haematuria could be useful in detecting active kidney disease.
Note: Reproducció del document publicat a: https://doi.org/10.1093/ckj/sfac257
It is part of: Clinical Kidney Journal, 2022, vol. 16, num.4, p. 693-700
URI: http://hdl.handle.net/2445/207276
Related resource: https://doi.org/10.1093/ckj/sfac257
ISSN: 2048-8505
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Clíniques)

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