Preterm Birth and in Utero Exposure to Corticosteroids Are Associated With Increased Infection Risk in Children of Mothers With IBD

Author:

Vestergaard Thea12ORCID,Holm Meiltoft Ida1,Julsgaard Mette13ORCID,Bek Helmig Rikke4,Friedman Sonia5,Kelsen Jens12

Affiliation:

1. Department of Hepatology and Gastroenterology, Aarhus University Hospital , Aarhus , Denmark

2. Department of Clinical Medicine, Aarhus University , Aarhus , Denmark

3. Center for Molecular Prediction of Inflammatory Bowel Disease [PREDICT], Department of Clinical Medicine, Aalborg University , Copenhagen , Denmark

4. Department of Obstetrics and Gynecology, Aarhus University Hospital , Aarhus , Denmark

5. Tufts University School of Medicine, Division of Gastroenterology and Hepatology, Tufts Medical School , Boston, MA , USA

Abstract

Abstract Background Corticosteroids, thiopurines, and biologics may come into play during pregnancy in women with inflammatory bowel disease and potentially impact the developing fetal immune system. We aimed to assess the risk of serious infections in children stratified by in utero exposure to biologics and immunomodulators or concomitant treatment with corticosteroids. Methods All singleton IBD pregnancies between 2008 and 2022 at a tertiary IBD center in Denmark were included. Maternal and offspring demographics, maternal disease activity, antenatal medical treatment, and infant infections resulting in hospital admission were recorded after review of medical records. Results In 602 live births (99.0%), we registered exposure to antenatal treatment as follows: biological monotherapy (n = 61, 10.2%), thiopurines (n = 110, 17.9%), biologics and concomitant thiopurines (n = 63, 10.3%), and controls (ie, no treatment with biological and/or thiopurines; n = 369, 60.6%). Preterm delivery (<37 gestational weeks) and systemic steroid administration during the third trimester were associated with an increased risk of serious infection in the offspring immediately after birth (relative risk = 17.5; 95% confidence interval, 7.8-39.8; P < .001, and relative risk = 4.8; 95% confidence interval, 1.5-12.7; P = 0.003, respectively). Intra-uterine exposure to biologics or combination treatment were not associated with a statistically significant higher risk of serious infections compared with controls; however, combination treatment showed an inclination towards an increased risk across analyses. Conclusion Preterm birth and systemic corticosteroid administration late in pregnancy are significant risk factors for serious infections in the offspring of IBD mothers.

Funder

Aase og Ejnar Danielsens Fond

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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