Education, biological ageing, all-cause and cause-specific mortality and morbidity: UK biobank cohort study.

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State: Public
Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_16B007B382B9
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Education, biological ageing, all-cause and cause-specific mortality and morbidity: UK biobank cohort study.
Journal
EClinicalMedicine
Author(s)
Chadeau-Hyam M., Bodinier B., Vermeulen R., Karimi M., Zuber V., Castagné R., Elliott J., Muller D., Petrovic D., Whitaker M., Stringhini S., Tzoulaki I., Kivimäki M., Vineis P., Elliott P., Kelly-Irving M., Delpierre C.
ISSN
2589-5370 (Electronic)
ISSN-L
2589-5370
Publication state
Published
Issued date
12/2020
Peer-reviewed
Oui
Volume
29-30
Pages
100658
Language
english
Notes
Publication types: Journal Article
Publication Status: epublish
Abstract
Socioeconomic position as measured by education may be embodied and affect the functioning of key physiological systems. Links between social disadvantage, its biological imprint, and cause-specific mortality and morbidity have not been investigated in large populations, and yet may point towards areas for public health interventions beyond targeting individual behaviours.
Using data from 366,748 UK Biobank participants with 13 biomarker measurements, we calculated a Biological Health Score (BHS, ranging from 0 to 1) capturing the level of functioning of five physiological systems. Associations between BHS and incidence of cardiovascular disease (CVD) and cancer, and mortality from all, CVD, cancer, and external causes were examined. We explored the role of education in these associations. Mendelian randomisation using genetic evidence was used to triangulate these findings.
An increase in BHS of 0.1 was associated with all-cause (HR = 1.14 [1.12-1.16] and 1.09 [1.07-1.12] in men and women respectively), cancer (HR = 1.11 [1.09-1.14] and 1.07 [1.04-1.10]) and CVD (HR = 1.25 [1.20-1.31] and 1.21 [1.11-1.31]) mortality, CVD incidence (HR = 1.15 [1.13-1.16] and 1.17 [1.15-1.19]). These associations survived adjustment for education, lifestyle-behaviours, body mass index (BMI), co-morbidities and medical treatments. Mendelian randomisation further supported the link between the BHS and CVD incidence (HR = 1.31 [1.21-1.42]). The BHS contributed to CVD incidence prediction (age-adjusted C-statistic = 0.58), other than through education and health behaviours.
The BHS captures features of the embodiment of education, health behaviours, and more proximal unknown factors which all complementarily contribute to all-cause, cancer and CVD morbidity and premature death.
Keywords
Allostatic load mortality, Biological ageing, Biomarkers, Incidentpathologies, Mendelian randomisation, Prospective cohort, Social embedding, Uk biobank
Pubmed
Web of science
Open Access
Yes
Create date
25/01/2021 8:27
Last modification date
23/01/2024 7:21
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