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dc.contributor.authorRodrigo Calabia, Emilio 
dc.contributor.authorQuintana, Luis F.
dc.contributor.authorVázquez-Sánchez, Teresa
dc.contributor.authorSánchez-Fructuoso, Ana
dc.contributor.authorBuxeda, Anna
dc.contributor.authorGavela, Eva
dc.contributor.authorCazorla, Juan M.
dc.contributor.authorCabello, Sheila
dc.contributor.authorBeneyto, Isabel
dc.contributor.authorLópez-Oliva, María O.
dc.contributor.authorDiekmann, Fritz
dc.contributor.authorGómez-Ortega, José M.
dc.contributor.authorCalva Romero, Natividad
dc.contributor.authorPérez-Sáez, María J.
dc.contributor.authorSancho, Asunción
dc.contributor.authorMazuecos, Auxiliadora
dc.contributor.authorEspí-Reig, Jordi
dc.contributor.authorJiménez, Carlos
dc.contributor.authorHernández, Domingo
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-02-29T17:30:40Z
dc.date.available2024-02-29T17:30:40Z
dc.date.issued2024
dc.identifier.issn2048-8505
dc.identifier.issn2048-8513
dc.identifier.urihttps://hdl.handle.net/10902/32004
dc.description.abstractBackground: Immunoglobulin A nephropathy (IgAN) is the most frequent recurrent disease in kidney transplant recipients and its recurrence contributes to reducing graft survival. Several variables at the time of recurrence have been associated with a higher risk of graft loss. The presence of clinical or subclinical inflammation has been associated with a higher risk of kidney graft loss, but it is not precisely known how it influences the outcome of patients with recurrent IgAN. Methods: We performed a multicentre retrospective study including kidney transplant recipients with biopsy-proven recurrence of IgAN in which Banff and Oxford classification scores were available. 'Tubulo-interstitial inflammation' (TII) was defined when 't' or 'i' were ≥2. The main endpoint was progression to chronic kidney disease (CKD) stage 5 or to death censored-graft loss (CKD5/DCGL). Results: A total of 119 kidney transplant recipients with IgAN recurrence were included and 23 of them showed TII. Median follow-up was 102.9 months and 39 (32.8%) patients reached CKD5/DCGL. TII related to a higher risk of CKD5/DCGL (3 years 18.0% vs 45.3%, log-rank 7.588, P = .006). After multivariate analysis, TII remained related to the risk of CKD5/DCGL (HR 2.344, 95% CI 1.119?4.910, P = .024) independently of other histologic and clinical variables. Conclusions: In kidney transplant recipients with IgAN recurrence, TII contributes to increasing the risk of CKD5/DCGL independently of previously well-known variables. We suggest adding TII along with the Oxford classification to the clinical variables to identify recurrent IgAN patients at increased risk of graft loss who might benefit from intensified immunosuppression or specific IgAN therapies.es_ES
dc.description.sponsorshipWork in this report was supported by Instituto de Salud Carlos III (RICORS2040: RD21/0005/0010 and RD21/0005/0012). Acknowledgements: The authors acknowledge the valuable contribution of all collaborators of the ‘Grupo de Trasplante Renal de la Sociedad Española de Nefrología’ (SENTRA).es_ES
dc.format.extent8 p.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rights© The Author(s) 2023. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.sourceClinical Kidney Journal, 2024, 17(1), 1-8es_ES
dc.subject.otherGraft losses_ES
dc.subject.otherIgA nephropathyes_ES
dc.subject.otherInflammationes_ES
dc.subject.otherKidney transplantationes_ES
dc.subject.otherRecurrencees_ES
dc.titleTubulo-interstitial inflammation increases the risk of graft loss after the recurrence of IgA nephropathyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1093/ckj/sfad259es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1093/ckj/sfad259
dc.type.versionpublishedVersiones_ES


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Mostrar el registro sencillo

© The Author(s) 2023. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.Excepto si se señala otra cosa, la licencia del ítem se describe como © The Author(s) 2023. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.