HIV infection is associated with a less aggressive phenotype of inflammatory bowel disease. A multicenter study of the ENEIDA registry.

医学 炎症性肠病 人类免疫缺陷病毒(HIV) 疾病 多中心研究 内科学 表型 临床表型 免疫学 随机对照试验 生物化学 化学 基因
作者
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,L Madero,Beatriz Burgueño-Gómez,David Monfort,Gisela Torres,Marta Teller,Juan Ángel Ferrer Rosique
出处
期刊:The American Journal of Gastroenterology [Lippincott Williams & Wilkins]
卷期号:120 (2): 431-439
标识
DOI:10.14309/ajg.0000000000002965
摘要

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. 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. 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). 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.
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