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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1093/ecco-jcc/jjae178</dc:identifier><dc:language>eng</dc:language><dc:creator>López De-La-Cruz, Julia</dc:creator><dc:creator>Gomollón, Fernando</dc:creator><dc:creator>Louro, Javier</dc:creator><dc:creator>López Pérez, Juan</dc:creator><dc:creator>Nocito Colon, María Mercedes</dc:creator><dc:creator>Gallego Llera, Beatriz</dc:creator><dc:creator>García-Mateo, Sandra</dc:creator><dc:creator>Martínez-Domínguez, Samuel J</dc:creator><dc:creator>Aso Gonzalvo, María Concepción</dc:creator><dc:creator>Gargallo-Puyuelo, Carla J</dc:creator><dc:title>Impact of HLADQA1*05 and HLADQA1*03 on Safety and Loss of Response to Anti-Tumor Necrosis Factor in Patients With Inflammatory Bowel Disease</dc:title><dc:identifier>ART-2024-142601</dc:identifier><dc:description>Background: HLADQA1*05 is recently associated with heightened immunogenicity to anti-tumor necrosis factor (TNFα). We aimed to determine whether HLADQ1*05 is a risk factor for primary non-response, loss of response (LOR), or adverse events (AE) to first-line anti-TNFα in patients with inflammatory bowel disease.              
Methods: We performed a retrospective observational study enrolling biologic naïve patients with Crohn’s disease and ulcerative colitis who initiated adalimumab or infliximab from 2000 to 2021. HLA-DQA1 genotype was determined in all patients and immunogenicity in 98 patients.
Results: We enrolled 408 patients who started first-line infliximab (n = 211) and adalimumab (n = 197), with a mean follow-up of 7.6 years. Primary response at Week 24 occurred in 347 (85.0%), LOR in 133 (38.3%), and AE in 93 (22.8%). The HLADQA1*05 was identified in 185 (43.3%) patients. In multivariate analyses, no risk factors were identified for primary response. HLADQA1*05 was an independent risk factor for LOR (adjusted hazard ratio [aHR] = 1.80, 95% CI = 1.21-2.67) and immunogenicity (aOR = 3.44, 95% CI = 1.12-11.92). HLADQA1*03 was a protective factor against LOR (aHR = 0.42, 95% CI = 0.20-0.88). Stratified analysis by anti-TNF type showed that HLADQA1*05 increased the risk of LOR to infliximab but not to adalimumab and HLADQA1*03 decreased the risk of LOR to adalimumab but not to infliximab. Female sex, infliximab, and the co-presentation of at least one allele of the HLADQA1*03 and HLADQA1*05 were risk factors for AE.
Conclusions: HLADQA1*05 is associated with a higher risk of LOR and immunogenicity, particularly to infliximab. HLADQA1*03 seems to play a protective role against LOR, particularly adalimumab. Female sex and infliximab are risk factors for AE.</dc:description><dc:date>2024</dc:date><dc:source>http://zaguan.unizar.es/record/150543</dc:source><dc:doi>10.1093/ecco-jcc/jjae178</dc:doi><dc:identifier>http://zaguan.unizar.es/record/150543</dc:identifier><dc:identifier>oai:zaguan.unizar.es:150543</dc:identifier><dc:identifier.citation>Journal of Crohn's &amp; colitis 20 (2024), 1-10</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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