Publicação
Serum dipeptidyl peptidase 4 : a predictor of disease activity and prognosis in inflammatory bowel disease
| dc.contributor.author | Pinto Lopes, Pedro | |
| dc.contributor.author | Afonso, Joana | |
| dc.contributor.author | Pinto Lopes, Rui | |
| dc.contributor.author | Rocha, Cátia | |
| dc.contributor.author | Lago, Paula | |
| dc.contributor.author | Gonçalves, Raquel | |
| dc.contributor.author | Tavares de Sousa, Helena | |
| dc.contributor.author | Macedo, Guilherme | |
| dc.contributor.author | Camila Dias, Cláudia | |
| dc.contributor.author | Magro, Fernando | |
| dc.date.accessioned | 2020-10-28T12:09:09Z | |
| dc.date.available | 2020-10-28T12:09:09Z | |
| dc.date.issued | 2020 | |
| dc.description | © 2020 Crohn’s & Colitis Foundation. Published by Oxford University Press. All rights reserved. This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model. | pt_PT |
| dc.description | A correction has been published: Inflammatory Bowel Diseases, Volume 26, Issue 6, June 2020, Page e56, https://doi.org/10.1093/ibd/izaa058 | pt_PT |
| dc.description.abstract | Background: Serum dipeptidyl peptidase 4 (DPP-4) has drawn particular interest as a biomarker in inflammatory bowel disease (IBD), as this protease inactivates several peptides that participate in the inflammatory cascade. Methods: Two prospectively recruited cohorts consisting of 195 patients (101 had Crohn’s disease [CD] and 94 had ulcerative colitis [UC]) were evaluated using clinical indexes and followed up to assess for treatment escalation. Sixty-eight patients underwent endoscopic evaluation at baseline. In the second cohort of 46 biologically treated patients, treatment response was assessed. Serum DPP-4, C-reactive protein (CRP), and fecal calprotectin levels were quantified at baseline and during follow-up. Results: Median DPP-4 levels were significantly lower in active IBD patients when compared with remitters (CD: 1043 [831–1412] vs 1589 [1255–1956] ng/mL; P < 0.001; UC: 1317 [1058–1718] vs 1798 [1329–2305] ng/mL; P = 0.001) and healthy controls (2175 [1875–3371] ng/mL). In fact, DPP-4 was able to distinguish clinical and endoscopic activity from remission, with areas under the curve (AUC) of 0.81/0.93 (CD) and 0.71/0.79 (UC), along with the need for treatment escalation, with comparable AUCs of 0.79 (CD) and 0.77 (UC). Furthermore, DPP-4 levels were higher in responders to treatment and more pronounced among UC (1467 [1301–1641] vs 1211 [1011–1448] ng/mL; P < 0.001) than CD patients (1385 [1185–1592] vs 1134 [975–1469] ng/mL; P = 0.015). Conclusions: Our results suggest that serum DPP-4 can be used as a noninvasive biomarker of IBD activity and biological treatment response and a predictor of treatment escalation, particularly when combined with other biomarkers. | pt_PT |
| dc.description.sponsorship | This work was supported by the Portuguese IBD Study Group (Grupo de Estudo da Doença Inflamatória Intestinal [GEDII]) and a research grant from Janssen-Cilag Pharmaceuticals. C.R. would like to acknowledge funding from “Fundação para a Ciência e Tecnologia (FCT),” Portugal, under grant number PDE/BDE/114583/2016 | pt_PT |
| dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
| dc.identifier.citation | Inflammatory Bowel Diseases, Volume 26, Issue 11, November 2020, pp. 1707–1719 | pt_PT |
| dc.identifier.doi | 10.1093/ibd/izz319 | pt_PT |
| dc.identifier.eissn | 1536-4844 | |
| dc.identifier.issn | 1078-0998 | |
| dc.identifier.uri | http://hdl.handle.net/10451/44691 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.publisher | Oxford University Press | pt_PT |
| dc.relation | Novo título: “Anti-drug Antibodies” Anti-TNF pharmacokinetics: In vitro model | |
| dc.relation.publisherversion | https://academic.oup.com/ibdjournal | pt_PT |
| dc.subject | Biomarkers | pt_PT |
| dc.subject | Dipeptidyl peptidase 4 | pt_PT |
| dc.subject | Inflammatory bowel disease | pt_PT |
| dc.title | Serum dipeptidyl peptidase 4 : a predictor of disease activity and prognosis in inflammatory bowel disease | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.awardTitle | Novo título: “Anti-drug Antibodies” Anti-TNF pharmacokinetics: In vitro model | |
| oaire.awardURI | info:eu-repo/grantAgreement/FCT//PDE%2FBDE%2F114583%2F2016/PT | |
| oaire.citation.endPage | 1719 | pt_PT |
| oaire.citation.issue | 11 | pt_PT |
| oaire.citation.startPage | 1707 | pt_PT |
| oaire.citation.title | Inflammatory Bowel Diseases | pt_PT |
| oaire.citation.volume | 26 | pt_PT |
| person.familyName | Pinto Lopes | |
| person.familyName | Afonso | |
| person.givenName | Pedro | |
| person.givenName | Joana | |
| person.identifier.orcid | 0000-0001-8450-8642 | |
| person.identifier.orcid | 0000-0001-9941-0613 | |
| person.identifier.rid | A-4395-2016 | |
| person.identifier.scopus-author-id | 35338892800 | |
| project.funder.identifier | http://doi.org/10.13039/501100001871 | |
| project.funder.name | Fundação para a Ciência e a Tecnologia | |
| rcaap.rights | restrictedAccess | pt_PT |
| rcaap.type | article | pt_PT |
| relation.isAuthorOfPublication | 9e9c2bcc-fd99-402e-ab9d-e3dda2d5f637 | |
| relation.isAuthorOfPublication | 7b999928-1a2d-435f-adf4-764aaccc9a4e | |
| relation.isAuthorOfPublication.latestForDiscovery | 9e9c2bcc-fd99-402e-ab9d-e3dda2d5f637 | |
| relation.isProjectOfPublication | 4b777985-b651-476e-9f51-4960b5b4e98a | |
| relation.isProjectOfPublication.latestForDiscovery | 4b777985-b651-476e-9f51-4960b5b4e98a |
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