Please use this identifier to cite or link to this item: https://hdl.handle.net/10620/19040
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dc.contributor.authorPriest, Naomi-
dc.contributor.authorGuo, Shuaijun-
dc.contributor.authorGondek, Dawid-
dc.contributor.authorLacey, Rebecca-
dc.contributor.authorBurgner, David-
dc.contributor.authorDownes, Marnie-
dc.contributor.authorSlopen, Natalie-
dc.contributor.authorGoldfeld, Sharon-
dc.contributor.authorMoreno-Betancur, Margarita-
dc.contributor.authorKerr, Jessica A-
dc.contributor.authorCahill, Stephanie-
dc.contributor.authorWake, Melissa-
dc.contributor.authorJuonala, Markus-
dc.contributor.authorLycett, Kate-
dc.contributor.authorO'Connor, Meredith-
dc.date.accessioned2022-11-22T04:19:43Z-
dc.date.available2022-11-22T04:19:43Z-
dc.date.issued2022-12-
dc.identifier.urihttps://hdl.handle.net/10620/19040-
dc.description.abstractBackground 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.en
dc.titleThe effect of adverse and positive experiences on inflammatory markers in Australian and UK childrenen
dc.typeJournal Articlesen
dc.identifier.doihttps://doi.org/10.1016/j.bbih.2022.100550en
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S2666354622001405en
local.contributor.institutionAustralian National Universityen
dc.identifier.surveyLSACen
dc.description.keywordsAdversityen
dc.description.keywordsPositive experiencesen
dc.description.keywordsInflammationen
dc.description.keywordsLongitudinalen
dc.description.keywordsLSACen
dc.description.keywordsALSPACen
dc.identifier.volume26en
dc.description.pages100550en
local.profile.orcid0000-0002-2246-0644en
local.identifier.emailnaomi.priest@anu.edu.auen
dc.title.bookBrain, Behavior, & Immunity - Healthen
dc.subject.dssDisadvantage, adversity and resilienceen
dc.subject.dssChildhood and child developmenten
dc.subject.dssHealth and wellbeingen
dc.relation.surveyLSACen
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Articles-
item.grantfulltextopen-
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