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dc.contributor.authorKezios, KL
dc.contributor.authorSuglia, SF
dc.contributor.authorDoyle, DM
dc.contributor.authorSusser, E
dc.contributor.authorBradwin, G
dc.contributor.authorCirillo, P
dc.contributor.authorCohn, B
dc.contributor.authorLink, B
dc.contributor.authorFactor-Litvak, P
dc.date.accessioned2022-02-17T14:56:23Z
dc.date.issued2022-02-12
dc.date.updated2022-02-17T13:46:32Z
dc.description.abstractSince its conceptualization, there has been a lack of consensus on the best way to operationalize allostatic load (AL). As a marker of the cumulative, physiological wear and tear on the body resulting from chronic exposure to stressors, it follows that AL should be higher among people who have faced more stressful life experiences. Thus, the purpose of this study was to construct AL scores using different operationalizations and, as a measure of construct validity, compare whether each construction produced expected disparities in AL by race and a composite socioeconomic status (SES) variable which accounts for measures over the life course; we also explored differences by sex. We conducted the study in a sample of 45-52-year-old offspring from the Child Health and Development Studies, a longitudinal birth cohort established in the early 1960s. AL scores were constructed in 6 different ways and included 10 biomarkers from inflammatory, neuroendocrine, cardiovascular, and metabolic systems. Our main approach to constructing AL was to sum across high-risk biomarker quartiles, correct for medication use, and use sex-specific high-risk quartiles for specific biomarkers. Alternative constructions did not use sex-specific quartiles and/or weighted biomarkers within subsystems and/or did not correct for medication use. We estimated differences in AL scores by race, SES, sex and their pairwise interactions. All constructions of AL, including the main approach, produced expected disparities by race (higher scores for Black vs. non-Black participants) and life course SES (higher scores for low vs. high SES participants). However, disparities by sex only emerged when the AL score was constructed via approaches that did not use sex-specific high-risk quartiles; for these alternative constructions, overall, female participants had higher AL scores than male participants and Black female participants had the highest AL scores in the sample. For most constructions, the pairwise interaction between sex and SES, showed a stronger disparity in AL scores between low and high-SES female compared with low- and high-SES male participants; this suggests that high life course SES may be more important for female (in terms of lowering AL) than male participants. In conclusion, our results suggest that the basic AL concept is consistently expressed in different operationalizations, making it an especially useful and robust tool for understanding disparities by race and SES.en_GB
dc.description.sponsorshipNational Institute for Child Health and Development (NICHD)en_GB
dc.description.sponsorshipNational Institute of Environmental Health Sciencesen_GB
dc.format.extent105689-
dc.identifier.citationArticle 105689en_GB
dc.identifier.doihttps://doi.org/10.1016/j.psyneuen.2022.105689
dc.identifier.grantnumberR01HD058515en_GB
dc.identifier.grantnumberT32-ES02377en_GB
dc.identifier.urihttp://hdl.handle.net/10871/128842
dc.identifierORCID: 0000-0002-8010-6870 (Doyle, David Matthew)
dc.language.isoenen_GB
dc.publisherElsevier / International Society of Psychoneuroendocrinologyen_GB
dc.rights.embargoreasonUnder embargo until 12 February 2023 in compliance with publisher policyen_GB
dc.rights© 2022 Published by Elsevier. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dc.subjectAllostatic loaden_GB
dc.subjectpatternsen_GB
dc.subjectdisparitiesen_GB
dc.subjectlife courseen_GB
dc.titleComparing different operationalizations of allostatic load measured in mid-life and their patterning by race and cumulative life course socioeconomic statusen_GB
dc.typeArticleen_GB
dc.date.available2022-02-17T14:56:23Z
dc.identifier.issn0306-4530
exeter.article-number105689
dc.descriptionThis is the author accepted manuscript. The final version is available from Elsevier via the DOI in this recorden_GB
dc.identifier.journalPsychoneuroendocrinologyen_GB
dc.relation.ispartofPsychoneuroendocrinology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dcterms.dateAccepted2022-02-10
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2022-02-12
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-02-17T14:52:56Z
refterms.versionFCDAM
refterms.panelAen_GB


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© 2022 Published by Elsevier. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  
Except where otherwise noted, this item's licence is described as © 2022 Published by Elsevier. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/