Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/221585
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dc.contributor.authorJiménez Blanco, Marta-
dc.contributor.authorCrespo Leiro, María G.-
dc.contributor.authorGarcía Cosío, María Dolores-
dc.contributor.authorGómez Bueno, Manuel-
dc.contributor.authorLópez Vilella, Raquel-
dc.contributor.authorOrtiz Bautista, Carlos-
dc.contributor.authorFarrero, Marta-
dc.contributor.authorZegrí Reiriz, Isabel-
dc.contributor.authorDíaz Molina, Beatriz-
dc.contributor.authorGarcía Romero, Elena-
dc.contributor.authorRangel Sousa, Diego-
dc.contributor.authorSalterain, Nahikari-
dc.contributor.authorGarrido Bravo, Iris-
dc.contributor.authorSegovia Cubero, Javier-
dc.date.accessioned2025-06-17T09:47:21Z-
dc.date.available2025-06-17T09:47:21Z-
dc.date.issued2024-11-19-
dc.identifier.issn1557-3117-
dc.identifier.urihttps://hdl.handle.net/2445/221585-
dc.description.abstractBACKGROUND: There is a long-standing need for a noninvasive biomarker that allows monitoring of cardiac allograft rejection, avoiding the need for periodic endomyocardial biopsies (EMB). METHODS: Multicenter, observational, prospective study, performed between 2019 and 2023 (NCT 04973943). All patients underwent 7 per-protocol surveillance EMB during the first postheart transplantation year. Donor-derived cell-free DNA (dd-cfDNA) levels were determined before each EMB, using Next Generation Sequencing Technology (Allonext assay, Eurofins Genome). The primary end-point was the association between dd-cfDNA levels and the presence of acute cellular rejection (ACR) in EMB. RESULTS: The study included 206 patients from 12 centers, with 1,090 pairs of EMB/dd-cfDNA determinations available for analysis. EMB with ACR (n = 49) were associated with dd-cfDNA levels significantly higher than those without, median 0.189% (interquartilic range 0.05-0.70) vs 0.095% (0.04-0.23), p = 0.013. A dd-cfDNA threshold of 0.10% showed a negative predictive value for ACR of 97%. A statistically significant association between N-terminal prohormone of brain (NTProBNP) and dd-cfDNA was also found, with an increase of 0.007% dd-cfDNA (95% confidence interval 0.003-0.011) for every 500 units of NTproBNP, p 0.001. The combination of both biomarkers for diagnosis of ACR showed an area under the receiver operating characteristic (ROC) curve of 0.681, and this combined approach was significantly better than dd-cfDNA alone (area under the ROC curve 0.603), p = 0.016. Using a cut-off point of 0.10% for dd-cfDNA and 1,000 UI/ml for NTproBNP, negative predictive value increased to 98.1%. CONCLUSIONS: dd-cfDNA may be a useful biomarker to rule out significant ACR in a low-risk population. However, a dd-cfDNA value above normal threshold does not correlate robustly with the presence of disease. The combination with NTproBNP, a readily available biomarker, increased the discrimination power of dd-cfDNA alone. CLINICAL TRIAL NOTATION: Donor-derived Cell-Free DNA as a New Biomarker in Cardiac Acute Rejection, NCT 04973943. J Heart Lung Transplant 2025;44:560-569 (c) 2024 The Authors. Published by Elsevier Inc. on behalf of International Society for Heart and Lung Transplantation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).-
dc.format.extent10 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier BV-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.healun.2024.11.009-
dc.relation.ispartofThe Journal of Heart and Lung Transplantation, 2024, vol. 44, num. 4, p. 560-569-
dc.relation.urihttps://doi.org/10.1016/j.healun.2024.11.009-
dc.rightscc-by-nc-nd (c) Jiménez Blanco et al., 2024-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationMarcadors bioquímics-
dc.subject.classificationTrasplantament cardíac-
dc.subject.classificationRebuig (Biologia)-
dc.subject.otherBiochemical markers-
dc.subject.otherHeart transplantation-
dc.subject.otherGraft rejection-
dc.titleDonor-derived cell-free DNA as a new biomarker for cardiac allograft rejection: A prospective study (FreeDNA-CAR)-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2025-06-06T11:30:52Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid39577511-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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