Validation of Calprotectin As a Novel Biomarker For The Diagnosis of Pleural Effusion: a Multicentre Trial.
Aged
Aged, 80 and over
Area Under Curve
Biomarkers, Tumor
/ analysis
Diagnosis, Differential
Female
Humans
Leukocyte L1 Antigen Complex
/ analysis
Male
Middle Aged
Pleura
/ pathology
Pleural Effusion
/ diagnosis
Pleural Effusion, Malignant
/ diagnosis
ROC Curve
Reproducibility of Results
Sensitivity and Specificity
Spain
/ epidemiology
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
30 03 2020
30 03 2020
Historique:
received:
15
01
2019
accepted:
08
03
2020
entrez:
2
4
2020
pubmed:
2
4
2020
medline:
2
12
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 32231227
doi: 10.1038/s41598-020-62388-y
pii: 10.1038/s41598-020-62388-y
pmc: PMC7105479
doi:
Substances chimiques
Biomarkers, Tumor
0
Leukocyte L1 Antigen Complex
0
Types de publication
Clinical Trial
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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