Role of Salmonella enterica exposure in Chilean Crohn's disease patients

To study the association between exposure to Salmonella enterica (SE) and Crohn's disease (CD) and its clinical implications in Chilean patients. Ninety-four unrelated Chilean CD patients from CAREI (Active Cohort Registry of Inflammatory Bowel Disease) presenting to a single inflammatory bowel...

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Published inWorld journal of gastroenterology : WJG Vol. 19; no. 35; pp. 5855 - 5862
Main Authors Alvarez-Lobos, Manuel, Pizarro, Daniela P, Palavecino, Christian E, Espinoza, Abner, Sebastián, Valentina P, Alvarado, Juan C, Ibañez, Patricio, Quintana, Carlos, Díaz, Orlando, Kalergis, Alexis M, Bueno, Susan M
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Co., Limited 21.09.2013
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Summary:To study the association between exposure to Salmonella enterica (SE) and Crohn's disease (CD) and its clinical implications in Chilean patients. Ninety-four unrelated Chilean CD patients from CAREI (Active Cohort Registry of Inflammatory Bowel Disease) presenting to a single inflammatory bowel disease (IBD) unit of a University Hospital were prospectively included in this study. A complete clinical evaluation, including smoking history, was performed at the initial visit, and all the important data of clinical evolution of CD were obtained. Blood samples from these CD patients and 88 healthy sex- and age-matched control subjects were analyzed for exposure to SE and for their NOD2/CARD15 gene status using the presence of anti-Salmonella lipopolysaccharide antibodies [immunoglobulin-G type (IgG)] and polymerase chain reaction (PCR), respectively. We also evaluated exposure to SE in 90 sex- and age-matched patients without CD, but with known smoking status (30 smokers, 30 non-smokers, and 30 former smokers). CD patients comprised 54 females and 40 males, aged 35.5 ± 15.2 years at diagnosis with a mean follow-up of 9.0 ± 6.8 years. CD was inflammatory in 59 patients (62.7%), stricturing in 24 (25.5%) and penetrating in 15 (15.5%). Thirty cases (31.9%) had lesions in the ileum, 29 (30.8%) had ileocolonic lesions, 32 (34.0%) had colonic lesions and 23 (24.4%) had perianal disease. Sixteen CD patients (17%) were exposed to SE compared to 15 (17%) of 88 healthy control subjects (P = 0.8). Thirty-one CD patients (32.9%) were smokers, and 7 (7.4%) were former smokers at diagnosis. In the group exposed to SE, 10 of 16 patients (62.5%) were active smokers compared to 21 of 78 patients (26.9%) in the unexposed group (P = 0.01). On the other hand, 10 of 31 smoking patients (32%) were exposed to SE compared to 5 of 56 nonsmoking patients (9%), and one of the seven former smokers (14%) (P = 0.01). In the group of 90 patients without CD, but whose smoking status was known, there was no difference in exposure to SE [3 of 30 smokers (10%), 5 of 30 non-smokers (16%), and 5 of 30 former smokers (16%); P = 0.6]. There were no differences in disease severity between CD patients with and those without anti-SE IgG antibodies, estimated as the appearance of stricturing [2 (12.5%) vs 22 (28.2%); P = 0.2] or penetrating lesions [2 (12.5%) vs 13 (16.6%); P = 1.0]; or the need for immunosuppressants [11 (68.7%) vs 55 (70.5%); P = 1.0], anti-tumor necrosis factor therapy [1 (6.2%) vs 7 (8.9%); P = 1.0], hospitalization [13 (81.2%) vs 58 (74.3%); P = 0.7], or surgery [3 (18.7%) vs 12 (15.3%); P = 0.3), respectively]. No other factors were associated with SE, including NOD2/CARD15 gene status. Seventeen CD patients (18%) had at least one mutation of the NOD2/CARD15 gene. Our study found no association between exposure to SE and CD. We observed a positive correlation between SE exposure and cigarette smoking in Chilean patients with CD, but not with disease severity.
Bibliography:Author contributions: Alvarez-Lobos M and Pizarro DP contributed equally to this work; Alvarez-Lobos M, Kalergis AM and Bueno SM designed the research; Alvarez-Lobos M, Pizarro DP, Palavecino CE, Espinoza A, Sebastian VP, Alvarado JC, Ibañez P, Quintana C, Díaz O and Bueno SM performed the research; Díaz O contributed new reagents and analytic tools; Alvarez-Lobos M, Pizarro DP, Alvarado JC, Ibañez P, Quintana C, Kalergis AM and Bueno SM analyzed the data; Alvarez-Lobos M, Pizarro DP, Ibañez P, Kalergis AM and Bueno SM wrote the paper and provided financial support for this work.
Correspondence to: Susan M Bueno, PhD, Millennium Institute on Immunology and Immunotherapy, Department of Molecular Genetics and Microbiology, School of Biological Sciences, Pontificia Universidad Católica de Chile, Avenida Libertador Bernardo OHiggins 340, Santiago 8331150, Chile. sbueno@bio.puc.cl
Telephone: +56-2-26862842 Fax: +56-2-26862185
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v19.i35.5855