Margalida Calafat, Carles Suria, Francisco Mesonero, Ruth de Francisco, Carmen Yagüe Caballero, Luisa de la Peña, Alejandro Hernández-Camba, Ainhoa Marcé, Beatriz Gallego, Noelia Martín-Vicente, Montserrat Rivero, Marisa Iborra, Iván Guerra, Marta Carrillo-Palau, Lucía Madero, Beatriz Burgueño, David Monfort, Gisela Torres, Marta Teller, Juan Ángel Ferrer Rosique, Pablo Vega Villaamil, Cristina Roig, Angel Ponferrada-Diaz, Elena Betoré Glaría, Yamile Zabana, Javier P Gisbert, David Busquets, Noelia Alcaide, Blau Camps, Jesús Legido, Maria González-Vivo, Marta Maia Bosca-Watts, Isabel Pérez-Martínez, Diego Casas Deza, Jordi Guardiola, Laura Arranz Hernández, Mercè Navarro, Carla J Gargallo-Puyuelo, Fiorella Cañete, Míriam Mañosa, Eugeni Domènech
{"title":"HIV Infection Is Associated With a Less Aggressive Phenotype of Inflammatory Bowel Disease: A Multicenter Study of the ENEIDA Registry.","authors":"Margalida Calafat, Carles Suria, Francisco Mesonero, Ruth de Francisco, Carmen Yagüe Caballero, Luisa de la Peña, Alejandro Hernández-Camba, Ainhoa Marcé, Beatriz Gallego, Noelia Martín-Vicente, Montserrat Rivero, Marisa Iborra, Iván Guerra, Marta Carrillo-Palau, Lucía Madero, Beatriz Burgueño, David Monfort, Gisela Torres, Marta Teller, Juan Ángel Ferrer Rosique, Pablo Vega Villaamil, Cristina Roig, Angel Ponferrada-Diaz, Elena Betoré Glaría, Yamile Zabana, Javier P Gisbert, David Busquets, Noelia Alcaide, Blau Camps, Jesús Legido, Maria González-Vivo, Marta Maia Bosca-Watts, Isabel Pérez-Martínez, Diego Casas Deza, Jordi Guardiola, Laura Arranz Hernández, Mercè Navarro, Carla J Gargallo-Puyuelo, Fiorella Cañete, Míriam Mañosa, Eugeni Domènech","doi":"10.14309/ajg.0000000000002965","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The coexistence of HIV infection and inflammatory bowel disease (IBD) is uncommon. Data on the impact of HIV on IBD course and its management are scarce. The aim of this study was to describe the IBD phenotype, therapeutic requirements, and prevalence of opportunistic infections (OIs) in IBD patients with a coexistent HIV infection.</p><p><strong>Methods: </strong>Case-control, retrospective study includes all HIV-positive patients diagnosed with IBD in the Nationwide study on genetic and environmental determinants of inflammatory bowel disease registry. Patients with positive HIV serology (HIV-IBD) were compared with controls (HIV seronegative), matched 1:3 by year of IBD diagnosis, age, sex, and type of IBD.</p><p><strong>Results: </strong>A total of 364 patients (91 HIV-IBD and 273 IBD controls) were included. In the whole cohort, 58% had ulcerative colitis, 35% had Crohn's disease (CD), and 7% were IBD unclassified. The HIV-IBD group presented a significantly higher proportion of proctitis in ulcerative colitis and colonic location in CD but fewer extraintestinal manifestations than controls. Regarding treatments, nonbiological therapies (37.4% vs 57.9%; P = 0.001) and biologicals (26.4% vs 42.1%; P = 0.007), were used less frequently among patients in the HIV-IBD group. Conversely, patients with HIV-IBD developed more OI than controls, regardless of nonbiological therapy use. In the multivariate analysis, HIV infection (odds ratio 4.765, 95% confidence interval (CI) 2.48-9.14; P < 0.001) and having ≥1 comorbidity (OR 2.445, 95% CI 1.23-4.85; P = 0.010) were risk factors for developing OI, while CD was protective (OR 0.372, 95% CI 0.18-0.78; P = 0.009).</p><p><strong>Discussion: </strong>HIV infection seems to be associated with a less aggressive phenotype of IBD and a lesser use of nonbiological therapies and biologicals but entails a greater risk of developing OI.</p>","PeriodicalId":7608,"journal":{"name":"American Journal of Gastroenterology","volume":"120 2","pages":"431-439"},"PeriodicalIF":8.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Gastroenterology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14309/ajg.0000000000002965","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: The coexistence of HIV infection and inflammatory bowel disease (IBD) is uncommon. Data on the impact of HIV on IBD course and its management are scarce. The aim of this study was to describe the IBD phenotype, therapeutic requirements, and prevalence of opportunistic infections (OIs) in IBD patients with a coexistent HIV infection.
Methods: Case-control, retrospective study includes all HIV-positive patients diagnosed with IBD in the Nationwide study on genetic and environmental determinants of inflammatory bowel disease registry. Patients with positive HIV serology (HIV-IBD) were compared with controls (HIV seronegative), matched 1:3 by year of IBD diagnosis, age, sex, and type of IBD.
Results: A total of 364 patients (91 HIV-IBD and 273 IBD controls) were included. In the whole cohort, 58% had ulcerative colitis, 35% had Crohn's disease (CD), and 7% were IBD unclassified. The HIV-IBD group presented a significantly higher proportion of proctitis in ulcerative colitis and colonic location in CD but fewer extraintestinal manifestations than controls. Regarding treatments, nonbiological therapies (37.4% vs 57.9%; P = 0.001) and biologicals (26.4% vs 42.1%; P = 0.007), were used less frequently among patients in the HIV-IBD group. Conversely, patients with HIV-IBD developed more OI than controls, regardless of nonbiological therapy use. In the multivariate analysis, HIV infection (odds ratio 4.765, 95% confidence interval (CI) 2.48-9.14; P < 0.001) and having ≥1 comorbidity (OR 2.445, 95% CI 1.23-4.85; P = 0.010) were risk factors for developing OI, while CD was protective (OR 0.372, 95% CI 0.18-0.78; P = 0.009).
Discussion: HIV infection seems to be associated with a less aggressive phenotype of IBD and a lesser use of nonbiological therapies and biologicals but entails a greater risk of developing OI.
期刊介绍:
Published on behalf of the American College of Gastroenterology (ACG), The American Journal of Gastroenterology (AJG) stands as the foremost clinical journal in the fields of gastroenterology and hepatology. AJG offers practical and professional support to clinicians addressing the most prevalent gastroenterological disorders in patients.