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
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引用次数: 0
摘要
导言:艾滋病病毒感染与炎症性肠病(IBD)并存的情况并不常见。有关 HIV 对 IBD 病程及其治疗的影响的数据很少。本研究旨在描述同时感染 HIV 的 IBD 患者的 IBD 表型、治疗要求和机会性感染(OIs)的发生率:病例对照、回顾性研究包括全国炎症性肠病遗传与环境决定因素研究登记中所有被诊断为 IBD 的 HIV 阳性患者。将艾滋病毒血清学呈阳性的患者(HIV-IBD)与对照组(艾滋病毒血清阴性)进行比较,按照 IBD 诊断年份、年龄、性别和 IBD 类型进行 1:3 匹配:共纳入了 364 名患者(91 名 HIV-IBD 患者和 273 名 IBD 对照组患者)。在整个队列中,58%患有溃疡性结肠炎,35%患有克罗恩病(CD),7%属于未分类的IBD。与对照组相比,HIV-IBD 组的溃疡性结肠炎患者直肠炎的比例和 CD 患者结肠部位的比例明显较高,但肠道外表现较少。在治疗方面,HIV-IBD 组患者较少使用非生物制剂疗法(37.4% vs 57.9%;P = 0.001)和生物制剂疗法(26.4% vs 42.1%;P = 0.007)。相反,与对照组相比,HIV-IBD 患者无论使用哪种非生物制剂治疗,都会出现更多的 OI。在多变量分析中,HIV 感染(几率比 4.765,95% 置信区间 (CI)2.48-9.14;P < 0.001)和合并症≥1(OR 2.445,95% CI 1.23-4.85;P = 0.010)是发生 OI 的风险因素,而 CD 具有保护作用(OR 0.372,95% CI 0.18-0.78;P = 0.009):讨论:HIV 感染似乎与侵袭性较低的 IBD 表型以及较少使用非生物制剂疗法和生物制剂有关,但却会增加罹患 OI 的风险。
HIV Infection Is Associated With a Less Aggressive Phenotype of Inflammatory Bowel Disease: A Multicenter Study of the ENEIDA Registry.
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.