dc.contributor.author | Botana Rial, María Isabel | |
dc.contributor.author | Vázquez Iglesias, Lorena | |
dc.contributor.author | Casado Rey, Pedro | |
dc.contributor.author | Páez de la Cadena Tortosa, María | |
dc.contributor.author | Andrade Olivié, María Amalia | |
dc.contributor.author | Abal Arca, José | |
dc.contributor.author | García Nimo, Laura | |
dc.contributor.author | Ferreiro Fernández, Lucía | |
dc.contributor.author | Valdés Cuadrado, Luis | |
dc.contributor.author | San José, María Esther | |
dc.contributor.author | Rodríguez Berrocal, Francisco Javier | |
dc.contributor.author | Fernández Villar, Alberto | |
dc.date.accessioned | 2021-05-11T07:01:21Z | |
dc.date.available | 2021-05-11T07:01:21Z | |
dc.date.issued | 2020-03-30 | |
dc.identifier.citation | Scientific Reports, 10(1): 5679(2020) | spa |
dc.identifier.issn | 20452322 | |
dc.identifier.uri | http://hdl.handle.net/11093/2120 | |
dc.description.abstract | Discriminating between malignant pleural effusion (MPE) and benign pleural effusion (BPE) remains difficult. Thus, novel and efficient biomarkers are required for the diagnosis of pleural effusion (PE). The aim of this study was to validate calprotectin as a diagnostic biomarker of PE in clinical settings. A total of 425 patients were recruited, and the pleural fluid samples collected had BPE in 223 cases (53.7%) or MPE in 137 patients (33%). The samples were all analysed following the same previously validated clinical laboratory protocols and methodology. Calprotectin levels ranged from 772.48 to 3,163.8 ng/mL (median: 1,939 ng/mL) in MPE, and 3,216–24,000 ng/mL in BPE (median: 9,209 ng/mL; p < 0.01), with an area under the curve of 0.848 [95% CI: 0.810–0.886]. For a cut-off value of ≤ 6,233.2 ng/mL, we found 96% sensitivity and 60% specificity, with a negative and positive predictive value, and negative and positive likelihood ratios of 96%, 57%, 0.06, and 2.4, respectively. Multivariate analysis showed that low calprotectin levels was a better discriminator of PE than any other variable [OR 28.76 (p < 0.0001)]. Our results confirm that calprotectin is a new and useful diagnostic biomarker in patients with PE of uncertain aetiology which has potential applications in clinical practice because it may be a good complement to cytological methods. | en |
dc.description.sponsorship | Instituto de Salud Carlos III | Ref. PI13/01538 | spa |
dc.description.sponsorship | Xunta de Galicia | Ref. CN/2014 | spa |
dc.description.sponsorship | Asociación Española de Endoscopia Respiratoria y Neumología Intervencionista | Ref. 2015 | spa |
dc.description.sponsorship | Sociedade Galega de Patoloxía Respiratoria | Ref. 2014 | spa |
dc.description.sponsorship | Fundación Biomédica Galicia Sur | spa |
dc.language.iso | eng | en |
dc.publisher | Scientific Reports | spa |
dc.rights | Attribution 4.0 International (CC BY 4.0) | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.title | Validation of calprotectin as a novel biomarker for the diagnosis of pleural effusion: a multicentre trial | en |
dc.type | article | spa |
dc.rights.accessRights | openAccess | spa |
dc.identifier.doi | 10.1038/s41598-020-62388-y | |
dc.identifier.editor | http://www.nature.com/articles/s41598-020-62388-y | spa |
dc.publisher.departamento | Química Física | spa |
dc.publisher.grupoinvestigacion | NanoBioMateriais Funcionais | spa |
dc.publisher.grupoinvestigacion | Biomarcadores Moleculares | spa |
dc.subject.unesco | 2302.21 Biología Molecular | spa |
dc.subject.unesco | 2409 Genética | spa |
dc.subject.unesco | 32 Ciencias Médicas | spa |
dc.subject.unesco | 3207.13 Oncología | spa |
dc.date.updated | 2021-05-05T11:57:03Z | |
dc.computerCitation | pub_title=Scientific Reports|volume=10|journal_number=1|start_pag=5679|end_pag=8 | spa |
dc.references | We would like to thank Publibeca SEPAR 2016, Cecilia Mouronte-Roibás, and Ana Priegue Carrera at the Pulmonary Department, Hospital Álvaro Cunqueiro, EOXI Vigo, Spain, and the PneumoVigoI+I Research Group, Heath Research Institute, Galicia Sur, Spain. This project was funded by grant PI13/01538 (FIS-FEDER), from the Xunta de Galicia (CN/2014), AEER (2015), and SOGAPAR (2014). Lorena Vázquez was supported by funding from the Fundación Biomédica Galicia Sur and with SEPAR integrated research programs (PII Neumología Intervencionista 2015). | spa |