Aug 2026· Journal of Pediatric Gastroenterology and Nutrition - JPGN· 0 citations· 45 references
Medicine
TL;DR
This bi-national prospective cohort study found no support for the hypothesis that experiences of early-life adverse events increase the risk of inflammatory bowel disease (IBD).
Abstract
Objectives
The experience of childhood stressful or adverse life events is believed to imprint on immunological pathways and, therefore, might have lasting effects on inflammatory bowel disease (IBD) development. This study aimed to examine the association between experiences of early-life adverse events and later IBD risk.
Methods
We followed children in the Norwegian Mother, Father, and Child Cohort Study (MoBa) and All Babies in Southeast Sweden cohort (ABIS) from birth (1997-2009) and linked cohort data to national patient registers to identify IBD diagnoses through the end of 2024 and 2023, respectively. We included 111,293 participants with data on adverse life events reported during pregnancy, by age 1, or by age 3. Adverse life events included adverse maternal or familial events, such as divorce or loss of a family member, based on questionnaire data from the two prospective birth cohorts. Cox regression was used to estimate adjusted hazard ratios (aHRs) for IBD in children exposed versus unexposed to adverse maternal or family events, accounting for parental and child characteristics. Cohort-specific estimates were pooled using a random effects model.
Results
We identified 697 IBD events over 2,255,642 person-years of follow-up. Experience of maternal adverse events in pregnancy, reported by 22% of the mothers, was not associated with offspring IBD; pooled aHR 1.00 (95% confidence interval [CI] = 0.57-1.76), compared with no experience. Neither experience of adverse family events by age 1 year (pooled aHR 0.96, 95% CI = 0.80-1.15), nor by age 3 years (pooled aHR 0.99, 95% CI = 0.83-1.17) was associated with later IBD.
Conclusions
This bi-national prospective cohort study found no support for the hypothesis that experiences of early-life adverse events increase the risk of IBD.
Early-life exposure to pets or farm animals was not associated with offspring risk of IBD, suggesting that early-life animal exposure may not be a major determinant of disease development.
C. Balmer, Manasi Agrawal, A. V. Hansen et al.· Clinical Gastroenterology an...· 0 citations
Evidence of inequalities according to socioeconomic disadvantage and childhood adversity for multiple menstrual symptoms is found, although some associations were only observed in one generation and suggest that menstrual symptoms are disproportionately experienced by socially and socioeconomically disadvantaged women.
G. Sawyer, B. Farooq, K. Birnie et al.· medRxiv· 0 citations
Adverse childhood experiences (ACEs) are associated with deleterious health outcomes, including poorer cardiovascular health over the life course. This study assesses the association between cumulative ACE exposure and a composite set of select risk factors for cardiovascular disease measures among a sample of wo...
Alexander Testa, Karyn Fu, Jacqueline Lee et al.· BMC Public Health· 0 citations
BACKGROUND
Adverse childhood experiences (ACEs) are linked to long-term health risks, yet their association with chronic liver diseases (CLDs) and mediating roles of mental health, lifestyles, and socioeconomic status remain undefined. We aimed to investigate these associations.
METHODS
This prospective cohort study...
Objective To examine whether prospectively recorded maternal BMI in early pregnancy is associated with offspring multiple sclerosis (MS) risk, including childhood-onset and adult-onset MS. Design Nationwide population-based cohort study. Setting Swedish national health and demographic registers. Participants 1,524,863...
H. Xu, N. Razaz, K. Remaeus et al.· medRxiv· 0 citations
Maternal autoimmune diseases are associated with increased offspring mortality risk, with the excess risk primarily concentrated in early life and driven by deaths related to perinatal conditions and congenital malformations.
Huan Zhang, I. Janszky, E. Arkema et al.· EClinicalMedicine· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.