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Adverse childhood experiences and asthma: Trajectories in a national cohort

  • Kathrine Pape
  • , Whitney Cowell
  • , Camilla Sandal Sejbaek
  • , Niklas Worm Andersson
  • , Cecilie Svanes
  • , Henrik Albert Kolstad
  • , Xiaoqin Liu
  • , Karin Sørig Hougaard
  • , Rosalind J Wright
  • , Vivi Schlünssen
  • Departments of Pediatrics & Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Department of Clinical Pharmacology, Bispeberg and Frederiksberg Hospitals, Copenhagen, Denmark.
  • Department of Occupational Medicine, Haukeland University Hospital, Bergen, Norway.
  • Department of Clinical Medicine, Occupational Medicine, Aarhus University, Aarhus, Denmark.
  • NCRR - The National Centre for Register-based Research, Aarhus University, Aarhus, Denmark.
  • Department of Public Health, Danish Ramazzini Centre, Aarhus University, Aarhus, Denmark.
  • Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
  • Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Institute of Public Health, Copenhagen University, Copenhagen, Denmark.

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

OBJECTIVE: Research has linked early adverse childhood experiences (ACEs) with asthma development; however, existing studies have generally relied on parent report of exposure and outcome. We aimed to examine the association of early life ACEs with empirically determined trajectories of childhood asthma risk, using independent register information on both exposures and outcome.

METHODS: Based on nationwide registries, we established a study cohort of 466 556 children born in Denmark (1997-2004). We obtained information on ACEs during the first 2 years of life (bereavement, parental chronic somatic and/or mental illness) and childhood asthma diagnosis or medication use from birth through age 10 years from the Danish National Patient and Prescription Registries, respectively. We identified asthma phenotypes using group-based trajectory modelling. We then used multinomial logistic regression to examine the association between early ACEs and asthma phenotypes.

RESULTS: We identified four asthma phenotypes: non-asthmatic, early-onset transient, early-onset persistent and late-onset asthma. Girls with early-onset transient asthma (OR 1.13, 95% CI 1.04 to 1.24), early-onset persistent asthma (1.27, 95% CI 1.08 to 1.48) or late-onset asthma (OR 1.28, 95% CI 1.11 to 1.48) vs no asthma were more likely to have early life ACE exposure compared with girls without ACE exposure. Results were similar for boys who also had experienced early life ACEs with ORs of 1.16 (95% CI 1.08 to 1.25), 1.34 (95% CI 1.20 to 1.51) and 1.11 (95% CI 0.98 to 1.25), respectively.

CONCLUSION: In a nationwide-population study, we identified three childhood onset asthma phenotypes and found that ACEs early in life were associated with increased odds for each of these asthma phenotypes among both girls and boys.

Original languageEnglish
JournalThorax
Volume76
Pages (from-to)547-553
ISSN0040-6376
DOIs
Publication statusPublished - 25 Mar 2021

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