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Early life exposures as risk factors for non-esophageal eosinophilic gastrointestinal diseases

医学 嗜酸性食管炎 怀孕 儿科 嗜酸性 内科学 疾病 病理 遗传学 生物
作者
Elizabeth T. Jensen,Xiangfeng Dai,Ellyn Kodroff,Mary Jo Strobel,Amy Zicarelli,Sarah A. O. Gray,Amanda Cordell,Chelsea Anderson,Girish Hiremath,Evan S. Dellon
出处
期刊:Clinics and Research in Hepatology and Gastroenterology [Elsevier]
卷期号:47 (7): 102170-102170 被引量:2
标识
DOI:10.1016/j.clinre.2023.102170
摘要

Early life exposures increase risk of eosinophilic esophagitis (EoE), but it is unknown whether they contribute to increased risk for non-EoE eosinophilic gastrointestinal diseases (EGIDs). We aimed to assess the association between prenatal, antenatal, and early life factors and non-EoE EGIDs.We conducted a case-control study based in EGID Partners, an online patient-centered research network. Adults (≥18 years) with non-EoE EGIDs, caregivers of children <18 years of age with an EGID, and non-EGID adult controls were eligible. Subjects completed our Early Life Exposure Questionnaire, detailing maternal and early childhood exposures. We assessed for associations between non-EoE EGIDs and early life exposures, focusing on exposures previously evaluated in association with EoE.We analyzed 61 non-EoE EGID cases and 20 controls. Of the EGID cases, 14 had eosinophilic gastritis, 19 had eosinophilic enteritis, 6 had eosinophilic colitis, and 22 had multiple areas affected; additionally, 30 had esophageal involvement. Relative to controls, EGID cases were more likely to have had antenatal/perinatal pregnancy-related complications (43% vs 13%; p = 0.02), NICU admission (20% vs 0%; p = 0.03), and antibiotics in infancy (43% vs 10%; p = 0.01). With adjustment for age at diagnosis, we observed increased odds of an EGID for pregnancy complications (aOR 3.83; 95% CI: 0.99-14.9) and antibiotic use in infancy (aOR 7.65; 95% CI: 1.28-45.7).Early life factors, including pregnancy complications, NICU admission, and antibiotics in infancy, were associated with development of non-EoE EGIDs. The impact of early life exposures on non-EoE EGID pathogenic mechanisms should be investigated.
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