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dc.contributor.authorGuijarro, L.G.
dc.contributor.authorCano-Martínez, D.
dc.contributor.authorToledo-Lobo, M.V.
dc.contributor.authorRuiz-Llorente, L.
dc.contributor.authorChaparro, M.
dc.contributor.authorGuerra, I.
dc.contributor.authorIborra, M.
dc.contributor.authorCabriada, J.L.
dc.contributor.authorBujanda, L.
dc.contributor.authorTaxonera, C.
dc.contributor.authorGarcía-Sánchez, V.
dc.contributor.authorMarín-Jiménez, I.
dc.contributor.authorBarreiro de Acosta, Manuel 
dc.contributor.authorVera, I.
dc.contributor.authorMartín-Arranz, M.D.
dc.contributor.authorMesonero, F.
dc.contributor.authorSempere, L.
dc.contributor.authorGomollón, F.
dc.contributor.authorHinojosa, J.
dc.contributor.authorZoullas, S.
dc.contributor.authorMonserrat, J.
dc.contributor.authorMenor-Salvan, C.
dc.contributor.authorAlvarez-Mon, M.
dc.contributor.authorGisbert, J.P.
dc.contributor.authorOrtega, M.A.
dc.contributor.authorHernández-Breijo, B.
dc.date.accessioned2025-08-25T12:40:26Z
dc.date.available2025-08-25T12:40:26Z
dc.date.issued2022
dc.identifier.citationGuijarro LG, Cano-Martínez D, Toledo-Lobo MV, Ruiz-Llorente L, Chaparro M, Guerra I, et al. Evaluation of AIF-1 (Allograft Inflammatory Factor-1) as a Biomarker of Crohn's Disease Severity. Biomedicines. 2022;10(3).
dc.identifier.issn2227-9059
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/628972f9ffc02649ba306004*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20497
dc.description.abstractBackground: Recently, increased tissue levels of AIF-1 have been shown in experimental colitis, supporting its role in intestinal inflammation. Therefore, we studied the levels of AIF-1 in Crohn's disease (CD). Methods: This study included 33 patients with CD (14 men and 19 women) who participated in the PREDICROHN project, a prospective multicenter study of the Spanish Group of Inflammatory bowel disease (GETECCU). Results: This article demonstrates declines with respect to baseline levels of serum AIF-1 in Crohn's disease (CD) patients after 14 weeks of treatment with anti-TNFs. Furthermore, in patients with active CD (HB ? 5), serum AIF-1 levels were significantly higher than those in patients without activity (HB ? 4). The study of serum AIF-1 in the same cohort, revealed an area under the ROC curve (AUC) value of AUC = 0.66 (p = 0.014), while for the CRP (C-reactive protein), (AUC) value of 0.69 (p = 0.0066), indicating a similar ability to classify CD patients by their severity. However, the combination of data on serum levels of AIF-1 and CRP improves the predictive ability of these analyses for classifying CD patients as active (HB ? 5) or inactive (HB ? 4). When we used the odds ratio (OR) formula, we observed that patients with CRP > 5 mg/L or AIF-1 > 200 pg/mL or both conditions were 13 times more likely to show HB ? 5 (active CD) than were those with both markers below these thresholds. Conclusion: The development of an algorithm that includes serum levels of AIF-1 and CRP could be useful for assessing Crohn's disease severity.en
dc.description.sponsorshipThis research has been funded by grants from: Asociacion Espanola de Gastroenterologia (AEG), Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa (GETECCU), Instituto de Salud Carlos III (FIS12/02557 and PI13/00041) and Universidad de Alcala (32/2013, 22/2014, 26/2015) and B2017/BMD-3804 MITIC-CM (Comunidad de Madrid) and Halekulani S.L.en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleEvaluation of AIF-1 (Allograft Inflammatory Factor-1) as a Biomarker of Crohn's Disease Severity*
dc.typeArticleen
dc.authorsophosGuijarro, B. L. G.
dc.authorsophosCano-Martínez, D.
dc.authorsophosToledo-Lobo, M. V.
dc.authorsophosRuiz-Llorente, L.
dc.authorsophosChaparro, M.
dc.authorsophosGuerra, I.
dc.authorsophosIborra, M.
dc.authorsophosCabriada, J. L.
dc.authorsophosBujanda, L.
dc.authorsophosTaxonera, C.
dc.authorsophosGarcía-Sánchez, V.
dc.authorsophosMarín-Jiménez, I.
dc.authorsophosAcosta, M. B.
dc.authorsophosVera, I.
dc.authorsophosMartín-Arranz, M. D.
dc.authorsophosMesonero, F.
dc.authorsophosSempere, L.
dc.authorsophosGomollón, F.
dc.authorsophosHinojosa, J.
dc.authorsophosZoullas, S.
dc.authorsophosMonserrat, J.
dc.authorsophosMenor-Salvan, C.
dc.authorsophosAlvarez-Mon, M.
dc.authorsophosGisbert, J. P.
dc.authorsophosOrtega, M. A.
dc.authorsophosHernández, Breijo
dc.identifier.doi10.3390/biomedicines10030727
dc.identifier.sophos628972f9ffc02649ba306004
dc.issue.number3
dc.journal.titleBiomedicines*
dc.page.initialnull
dc.relation.projectIDAsociacion Espanola de Gastroenterologia (AEG); Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa (GETECCU); Instituto de Salud Carlos III [FIS12/02557, PI13/00041]; Universidad de Alcala [32/2013, 22/2014, 26/2015]; Comunidad de Madrid [B2017/BMD-3804 MITIC-CM]; Halekulani S.L
dc.relation.publisherversionhttps://www.mdpi.com/2227-9059/10/3/727/pdf?version=1648022117;https://mdpi-res.com/d_attachment/biomedicines/biomedicines-10-00727/article_deploy/biomedicines-10-00727-v2.pdf?version=1648022117es
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number10


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