How does socio-economic position (SEP) get biologically embedded? A comparison of allostatic load and the epigenetic clock(s).


Journal

Psychoneuroendocrinology
ISSN: 1873-3360
Titre abrégé: Psychoneuroendocrinology
Pays: England
ID NLM: 7612148

Informations de publication

Date de publication:
06 2019
Historique:
received: 12 10 2018
revised: 13 02 2019
accepted: 15 02 2019
pubmed: 1 3 2019
medline: 19 5 2020
entrez: 1 3 2019
Statut: ppublish

Résumé

Individuals of lower socio-economic position (SEP) carry a heavier burden of disease and morbidity and live shorter lives on average compared with their more advantaged counterparts. This has sparked research interest in the processes and mechanisms via which social adversity gets biologically embedded. The present study directly compares the empirical worth of two candidate mechanisms: Allostatic Load (AL) and the Epigenetic Clock(s) for advancing our understanding of embodiment using a sub-sample of 490 individuals from the Irish Longitudinal Study (TILDA) who were explicitly selected for this purpose based on their inter-generational life course social class trajectory. A battery of 14 biomarkers representing the activity of 4 different physiological systems: Immunological, Cardiovascular, Metabolic, and Renal was used to construct the AL score. Biomarkers were dichotomised into high and low risk groups according to sex-specific quartiles of risk and summed to create a count ranging from 0-14. Three measures of epigenetic age acceleration were computed according to three sets of age-associated Cytosine-phosphate-Guanine (CpG) sites described by Horvath, Hannum and Levine. AL was strongly socially patterned across a number of measures of SEP, while the epigenetic clocks were not. AL partially mediated the association between measures of SEP and an objective measure of physiological functioning: performance on the Timed Up and Go (TUG test). We conclude that AL may represent the more promising candidate for understanding the pervasive link between SEP and health.

Identifiants

pubmed: 30818253
pii: S0306-4530(18)31063-1
doi: 10.1016/j.psyneuen.2019.02.018
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

64-73

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Cathal McCrory (C)

The Irish Longitudinal Study on Ageing, Trinity College Dublin, Ireland. Electronic address: mccrorc@tcd.ie.

Giovanni Fiorito (G)

Italian Institute for Genomic Medicine (IIGM, former HuGeF), Italy.

Cliona Ni Cheallaigh (C)

The Irish Longitudinal Study on Ageing, Trinity College Dublin, Ireland.

Silvia Polidoro (S)

Italian Institute for Genomic Medicine (IIGM, former HuGeF), Italy.

Piia Karisola (P)

Faculty of Medicine, University of Helsinki, 00014, Helsinki, Finland.

Harri Alenius (H)

Faculty of Medicine, University of Helsinki, 00014, Helsinki, Finland; Institute of Environmental Medicine (IMM), Karolinska Institutet, Stockholm, Sweden.

Richard Layte (R)

Department of Sociology, Trinity College Dublin, Ireland.

Teresa Seeman (T)

David Geffen School of Medicine, UCLA, USA.

Paolo Vineis (P)

MRCPHE Centre for Environment and Health, Imperial College London, United Kingdom.

Rose Anne Kenny (RA)

The Irish Longitudinal Study on Ageing, Trinity College Dublin, Ireland.

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Classifications MeSH