Prenatal, Intrapartum, and Neonatal Factors Increase the Risk of Eosinophilic Esophagitis

Author:

Kurt Gencer1,Svane Helene M.L.1,Erichsen Rune12,Heide-Jørgensen Uffe1,Sørensen Henrik T.13,Dellon Evan S.3,Jensen Elizabeth T.345

Affiliation:

1. Department of Clinical Epidemiology, Aarhus University, Aarhus, Denmark;

2. Department of Surgery, Randers Regional Hospital, Randers, Denmark;

3. Center for Esophageal Diseases and Swallowing, Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA;

4. Department of Epidemiology and Prevention, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA;

5. Gastroenterology Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.

Abstract

INTRODUCTION: Early-life exposures have been associated with an increased risk of eosinophilic esophagitis (EoE); however, most studies to date have been conducted at referral centers and are subject to recall bias. By contrast, we conducted a nationwide, population-based and registry-based case-control study of prenatal, intrapartum, and neonatal exposures, using data collected prospectively through population-based Danish health and administrative registries. METHODS: We ascertained all EoE cases in Denmark (birth years 1997–2018). Cases were sex and age matched to controls (1:10) using risk-set sampling. We obtained data on prenatal, intrapartum, and neonatal factors, i.e., pregnancy complications, mode of delivery, gestational age at delivery, birthweight (expressed as a z-score), and neonatal intensive care unit (NICU) admission. We used conditional logistic regression to compute the crude and adjusted odds ratios (aOR) of EoE in relation to each prenatal, intrapartum, and neonatal factor, thus providing an estimate of incidence density ratios with 95% confidence intervals (CI). RESULTS: In the 393 cases and 3,659 population controls included (median age at index date, 11 years [interquartile range, 6–15]; 69% male), we observed an association between gestational age and EoE, peaking at 33 vs 40 weeks (aOR 3.6 [95% CI 1.8–7.4]), and between NICU admission and EoE (aOR 2.8 [95% CI 1.2–6.6], for a NICU hospitalization of 2–3 weeks vs no admission). In interaction analyses, we observed a stronger association between NICU admission and EoE in infants born at term than in preterm infants (aOR 2.0 [95% CI 1.4–2.9] for term infants and aOR 1.0 [95% CI 0.5–2.0] for preterm infants). We also observed an association between pregnancy complications and EoE (aOR 1.4 [95% CI 1.0–1.9]). Infants who were very growth restricted at birth had an increased rate of EoE (aOR 1.4 [95% CI: 1.0–1.9] for a z-score of −1.5 vs a z-score of 0). Mode of delivery was not associated with EoE. DISCUSSION: Prenatal, intrapartum, and neonatal factors, particularly preterm birth and NICU admission, were associated with development of EoE. Further research is needed to elucidate the mechanisms underlying the observed associations.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

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