Early life factors are associated with risk for eosinophilic esophagitis diagnosed in adulthood

Author:

Dellon Evan S12ORCID,Shaheen Olivia1,Koutlas Nathaniel T1,Chang Audrey O1,Martin Lisa J34,Rothenberg Marc E56,Jensen Elizabeth T256

Affiliation:

1. Center for Esophageal Diseases and Swallowing, University of North Carolina School of Medicine, Chapel Hill, NC, USA

2. Center for Gastrointestinal Biology and Disease, Division of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, USA

3. Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA

4. Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati OH, USA

5. Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, OH, USA

6. Wake Forest School of Medicine, Department of Epidemiology and Prevention, Winston-Salem, NC, USA

Abstract

SUMMARY Early life exposures have been associated with pediatric eosinophilic esophagitis (EoE), but it is unknown if a similar association is present in adults. We aimed to assess the association between early life risk factors and development of EoE in adulthood. To do this, we conducted a case–control study which was nested within a prospective cohort study of adults undergoing outpatient endoscopy. Cases of EoE were diagnosed per consensus guidelines; controls did not meet these criteria. Subjects and their mothers were contacted to collect information on four key early life exposures: antibiotics taken during the first year of life, Cesarean delivery, preterm delivery (≤37 weeks’ gestation), and neonatal intensive care unit (NICU) admission. We calculated the odds of EoE given in each exposure and assessed agreement between subjects and their mothers. For the 40 cases and 40 controls enrolled, we observed a positive association between each of the early life exposures and development of EoE (antibiotics in infancy, OR = 4.64, 95% CI = 1.63–13.2; Cesarean delivery, OR = 3.08, 95% CI = 0.75–12.6; preterm delivery, OR = 2.92, 95% CI = 0.71–12.0; NICU admission, OR = 4.00, 95% CI = 1.01–15.9). Results were unchanged after adjusting for potential confounders, though only early antibiotic use had CIs that did not cross 1.0. Moderate to strong agreement was observed between 54 subject–mother pairs (antibiotics, K = 0.44, P = 0.02; Cesarean delivery, K = 1.0, P < 0.001; preterm delivery, K = 0.80, P < 0.001; NICU, K = 0.76, P < 0.001). In sum, antibiotics in infancy was significantly associated with increased risk of EoE diagnosed in adulthood, while positive trends were seen with other early life factors such as Cesarean delivery, preterm delivery, and NICU admission. This may indicate persistent effects of early life exposures and merits additional study into conserved pathogenic mechanisms.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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