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Immigrant IBD Patients in Spain Are Younger, Have More Extraintestinal Manifestations and Use More Biologics Than Native Patients

Abstract

Background: Previous studies comparing immigrant ethnic groups and native patients with IBD have yielded clinical and phenotypic differences. To date, no study has focused on the immigrant IBD population in Spain.

Methods: Prospective, observational, multicenter study comparing cohorts of IBD patients from ENEIDA-registry who were born outside Spain with a cohort of native patients.

Results: We included 13,524 patients (1,864 immigrant and 11,660 native). The immigrants were younger (45 ± 12 vs. 54 ± 16 years, < 0.001), had been diagnosed younger (31 ± 12 vs. 36 ± 15 years, < 0.001), and had a shorter disease duration (14 ± 7 vs. 18 ± 8 years, < 0.001) than native patients. Family history of IBD (9 vs. 14%, < 0.001) and smoking (30 vs. 40%, < 0.001) were more frequent among native patients. The most prevalent ethnic groups among immigrants were Caucasian (41.5%), followed by Latin American (30.8%), Arab (18.3%), and Asian (6.7%). Extraintestinal manifestations, mainly musculoskeletal affections, were more frequent in immigrants (19 vs. 11%, < 0.001). Use of biologics, mainly anti-TNF, was greater in immigrants (36 vs. 29%, < 0.001). The risk of having extraintestinal manifestations [OR: 2.23 (1.92-2.58, < 0.001)] and using biologics [OR: 1.13 (1.0-1.26, = 0.042)] was independently associated with immigrant status in the multivariate analyses.

Conclusions: Compared with native-born patients, first-generation-immigrant IBD patients in Spain were younger at disease onset and showed an increased risk of having extraintestinal manifestations and using biologics. Our study suggests a featured phenotype of immigrant IBD patients in Spain, and constitutes a new landmark in the epidemiological characterization of immigrant IBD populations in Southern Europe.

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References
1.
Windsor J, Kaplan G . Evolving Epidemiology of IBD. Curr Gastroenterol Rep. 2019; 21(8):40. DOI: 10.1007/s11894-019-0705-6. View

2.
Juyal G, Amre D, Midha V, Sood A, Seidman E, Thelma B . Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians. Aliment Pharmacol Ther. 2007; 26(10):1325-32. DOI: 10.1111/j.1365-2036.2007.03524.x. View

3.
Bodiwala V, Marshall T, Das K, Brant S, Seril D . Comparison of Disease Phenotypes and Clinical Characteristics Among South Asian and White Patients with Inflammatory Bowel Disease at a Tertiary Referral Center. Inflamm Bowel Dis. 2020; 26(12):1869-1877. DOI: 10.1093/ibd/izaa019. View

4.
Kedia S, Ahuja V . Epidemiology of Inflammatory Bowel Disease in India: The Great Shift East. Inflamm Intest Dis. 2018; 2(2):102-115. PMC: 5988149. DOI: 10.1159/000465522. View

5.
Paredes Mendez J, Otoya Moreno G, Mestanza Rivas Plata A, Lazo Molina L, Acuna Ordonez K, Arenas Gamio J . [Epidemiological and clinical characteristics of inflammatory bowel disease in a tertiary referral hospital in Lima-Peru]. Rev Gastroenterol Peru. 2016; 36(3):209-218. View