Fecal intestinal inflammatory biomarkers in piglets

Analytical validation of biomarker assays as indicators of intestinal inflammatory processes is essential for the diagnosis, prognosis and monitoring of intestinal health. In the context of porcine intestinal health, feces are a sample of choice for determining inflammatory molecules released into t...

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Detalhes bibliográficos
Autores: Pelegrí i Pineda, Anna|||0009-0000-9997-5622, Pato, Raquel|||0000-0001-7358-0382, Peña Roman, Raquel|||0000-0002-7193-9141, Suppi, Júlia, Llauradó Calero, Eudald|||0000-0003-1644-3116, Solà Oriol, David|||0000-0001-8365-340X, Bassols Teixidó, Anna Maria|||0000-0003-4213-2274, Saco Rodriguez, Yolanda|||0000-0002-2482-9820
Formato: artículo
Fecha de publicación:2025
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:322297
Acesso em linha:https://ddd.uab.cat/record/322297
https://dx.doi.org/urn:doi:10.1016/j.vas.2025.100523
Access Level:acceso abierto
Palavra-chave:Porcine
Biomarker
Feces
Non-invasive
Intestinal inflammation
Sample homogeneity
Descrição
Resumo:Analytical validation of biomarker assays as indicators of intestinal inflammatory processes is essential for the diagnosis, prognosis and monitoring of intestinal health. In the context of porcine intestinal health, feces are a sample of choice for determining inflammatory molecules released into the intestinal contents in pathological conditions. The advantage of this method is that it is non-invasive and samples can be collected easily, quickly and without causing stress. In this study, we validated the analytical procedures for measuring lipocalin-2 (LCN-2), myeloperoxidase (MPO) and adenosine deaminase (ADA) in porcine fecal samples. Validation was carried out by studying precision (intra- and inter-assay coefficients of variation), linearity under dilution, recovery, and the limits of detection and quantification. All three biomarkers fulfilled the required validation parameters. Furthermore, we analyzed the distribution of the three compounds and calprotectin (fCal) in the stools and found that all of them except LCN-2 were homogeneously distributed in the fecal sample. The stability of the compounds under different storage temperatures was assessed, and fCal was found to be the most stable parameter overall.