The effect of adverse and positive experiences on inflammatory markers in Australian and UK children

Détails

ID Serval
serval:BIB_EA0F42EC960E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
The effect of adverse and positive experiences on inflammatory markers in Australian and UK children
Périodique
Brain, Behavior, & Immunity - Health
Auteur⸱e⸱s
Priest Naomi, Guo Shuaijun, Gondek Dawid, Lacey Rebecca E., Burgner David, Downes Marnie, Slopen Natalie, Goldfeld Sharon, Moreno-Betancur Margarita, Kerr Jessica A., Cahill Stephanie, Wake Melissa, Juonala Markus, Lycett Kate, O'Connor Meredith
ISSN
2666-3546
Statut éditorial
Publié
Date de publication
2022
Peer-reviewed
Oui
Volume
26
Pages
100550
Langue
anglais
Résumé
Background The relationship between childhood adversity and inflammation is well-established. Examination of positive experiences can provide a more complete understanding of intervention opportunities. We investigated associations of adverse and positive experiences, and their intersection, with inflammation in children and adolescents. Methods Data sources: Longitudinal Study of Australian Children (LSAC; N = 1237) and Avon Longitudinal Study of Parents and Children (ALSPAC; N = 3488). Exposures: Adverse and positive experiences assessed repeatedly (LSAC: 0–11 years; ALSPAC: 0–15 years). Outcomes: Inflammation quantified by high sensitivity C-reactive protein (hsCRP) and glycoprotein acetyls (GlycA) (LSAC: 11–12 years; ALSPAC: 15.5 years). Analyses: Linear regression on the log-transformed outcomes estimated the relative difference in inflammatory markers with adverse/positive experiences, adjusting for socio-demographics and concurrent positive/adverse experiences, respectively. Results Most associations were in the expected direction but differed in magnitude by exposure, outcome and cohort. Across both cohorts, adverse experiences were associated with up to 7.3% higher hsCRP (95% CI: −18.6%, 33.2%) and up to 2.0% higher GlycA (95% CI: 0.5%, 3.5%); while positive experiences were associated with up to 22.1% lower hsCRP (95% CI: −49.0%, 4.7%) and 1.3% lower GlycA (95% CI: −2.7%, 0.2%). In LSAC, the beneficial effect of positive experiences on inflammation was more pronounced among those with fewer concurrent adverse experiences. Conclusion Across two cohorts, we found small but directionally consistent associations between adverse experiences and higher inflammation, and positive experiences and lower inflammation, particularly for GlycA. Future research should give further consideration to positive experiences to complement the current focus on adversity and inform the design and evaluation of early life interventions.
Mots-clé
Adversity, Positive experiences, Inflammation, Longitudinal, LSAC, ALSPAC
Création de la notice
28/09/2023 8:29
Dernière modification de la notice
10/10/2023 10:27
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