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dc.contributorUniversitat de Vic - Universitat Central de Catalunya. Facultat de Ciències, Tecnologia i Enginyeries
dc.contributorUniversitat de Vic - Universitat Central de Catalunya. Facultat de Medicina
dc.contributorUniversitat de Vic - Universitat Central de Catalunya. Grup de recerca en Reparació i Regeneració Tissular (TR2Lab)
dc.contributorInstitut de Recerca i Innovació en Ciències de la Vida i de la Salut a la Catalunya Central (IRIS-CC)
dc.contributor.authorBérgamo, Silvia
dc.contributor.authorTrapé, Jaume
dc.contributor.authorGonzález-García, Laura
dc.contributor.authorGonzález Fernández, Carolina
dc.contributor.authorVergara, Carme
dc.contributor.authorde la Torre, Noelia
dc.contributor.authorTrujillo, Gloria
dc.contributor.authorEstivill, Dolors
dc.contributor.authorAlvarez-González, Marco Antonio
dc.contributor.authorBosch Presegué, Laia
dc.contributor.authorOtero Viñas, Marta
dc.contributor.authorBergós, Carmen
dc.contributor.authorCatot, Silvia
dc.contributor.authorSant Masoliver, Francesc
dc.date.accessioned2024-01-24T16:50:08Z
dc.date.available2024-01-24T16:50:08Z
dc.date.created2023
dc.date.issued2023
dc.identifier.citationBérgamo, S., Trapé, J., González-García, L., González-Fernández, C., Vergara, C., de-la-Torre, N., Trujillo, G., Estivill, D., Álvarez-González, M. A., Bosch, L., Otero-Viñas, M., Bergós, C., Catot, S., Ruiz-Hidalgo, D., Ros, S., Sant, F. (2023). Utility of human epididymis protein 4 in the differential diagnosis of ascites. Clinical Biochemistry, 120, num: 110645. https://doi.org/10.1016/j.clinbiochem.2023.110645es
dc.identifier.issn0009-9120
dc.identifier.urihttp://hdl.handle.net/10854/7670
dc.description.abstractBackground and aims: Human epididymal protein 4 (HE4) may be a useful tool in the differential diagnosis of malignant ascites. The aim of this study was to evaluate the diagnostic utility of HE4 for detecting malignant ascites, taking into account the possible false positives identified with adenosine deaminase (ADA), C-reactive protein (CRP), % polynuclear cells (%PMN) and glomerular filtration rate (eGFR).Methods: Concentrations of HE4, ADA, %PMN and CRP were determined in 114 samples of peritoneal fluid and creatinine in serum in order to calculate eGFR.Results: Concentrations of HE4 presented significant differences (P = 0.028) in benign [median (interquartile range)] [582(372)] pmol/L) and malignant ascites ([8241(367)] pmol/L. Sensitivity was 21.2% and specificity 100%. Significant differences were also observed for HE4 between tumors of gynecological origin ([3165(8769)] pmol/L) and others ([665(663)] pmol/L), with a sensitivity of 67% and a specificity of 100%. Classifying according to possible false positives (ADA > 45U/L, CRP > 50 mg/L, %PMN > 90 and eGFR < 30 mL/ min/1.73 m(2)) at maximum specificity, a sensitivity of 33.3% was obtained for HE4, with a cut-off point of 2660 pmol/L. Without possible false positives (ADA < 45U/L, CRP < 50 mg/L, %PMN < 90 and eGFR >= 30 mL/min/ 1.73 m(2)), a sensitivity of 37.7% was obtained at 100% specificity for a cut-off point of 1041 pmol/L. Applying these criteria to the entire group, a sensitivity of 36.4% was obtained at maximum specificity.Conclusions: HE4 allows the identification of malignant ascites with moderate sensitivity at maximum specificity. HE4 levels can differentiate between tumors of gynecological origin and others. Classification according to possible false positives increases sensitivity without losing specificity.es
dc.formatapplication/pdfes
dc.format.extent8 p.es
dc.language.isoenges
dc.publisherPergamon-Elsevier Sciencees
dc.rightsAquest document està subjecte a aquesta llicència Creative Commonses
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.caes
dc.subject.otherErrors de diagnòstices
dc.subject.otherMarcadors tumoralses
dc.titleUtility of human epididymis protein 4 in the differential diagnosis of asciteses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.1016/j.clinbiochem.2023.110645
dc.rights.accessRightsinfo:eu-repo/semantics/closedAccesses
dc.type.versioninfo:eu-repo/publishedVersiones
dc.indexacioIndexat a WOS/JCRes
dc.indexacioIndexat a SCOPUSes


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