Imperial College London

ProfessorPaoloVineis

Faculty of MedicineSchool of Public Health

Chair in Environmental Epidemiology
 
 
 
//

Contact

 

+44 (0)20 7594 3372p.vineis Website

 
 
//

Location

 

511Medical SchoolSt Mary's Campus

//

Summary

 

Publications

Citation

BibTex format

@article{Freni:2022:10.18632/aging.203872,
author = {Freni, Sterrantino A and Fiorito, G and D'errico, A and Oliver, R and Virtanen, M and Ala-Mursula, L and Jarvelin, MR and Ronkainen, J and Vineis, P},
doi = {10.18632/aging.203872},
journal = {Aging},
pages = {1128--1156},
title = {Work-related stress and well-being in association with epigenetic age acceleration: a Northern Finland Birth Cohort 1966 Study},
url = {http://dx.doi.org/10.18632/aging.203872},
volume = {14},
year = {2022}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Recent evidence indicates consistent association of low socioeconomic status with epigenetic age acceleration, measured from DNA methylation. As work characteristics and job stressors are crucial components of socioeconomic status, we investigated their association with various measures of epigenetic age acceleration.The study population included employed and unemployed men and women (n=604) from the Northern Finland Birth Cohort 1966. We investigated the association of job strain, effort-reward imbalance and work characteristics with five biomarkers of epigenetic aging (Hannum, Horvath, PhenoAge, GrimAge, and DunedinPoAm).Our results indicate few significant associations between work stress indicators and epigenetic age acceleration, limited to a range of ±2 years, and smoking recording the highest effect on GrimAge age acceleration biomarker between current and no smokers (median difference 4.73 years (IQR 1.18, 8.41). PhenoAgeAA was associated with job strain active work (β=-1.301 95%CI -2.391, -0.212), slowing aging of less than 1.5 years, and working as white-collar slowed aging six months (GrimAgeAA β=-0.683, 95%CI -1.264, -0.102) when compared to blue collars. Association was found for working for more than 40 hours per week that increased the aging over 1.5 years, (HorvathAA β =2.058 95%CI 0.517,3.599, HannumAA β=1.567, 95%CI 0.415,2.719).The pattern of associations was different between women and men and some of the estimated effects are inconsistent with current literature. Our results provide the first evidence of association of work conditions with epigenetic aging biomarkers. However, further epidemiological research is needed to fully understand how work-related stress affects epigenetic age acceleration in men and women in different societies.
AU - Freni,Sterrantino A
AU - Fiorito,G
AU - D'errico,A
AU - Oliver,R
AU - Virtanen,M
AU - Ala-Mursula,L
AU - Jarvelin,MR
AU - Ronkainen,J
AU - Vineis,P
DO - 10.18632/aging.203872
EP - 1156
PY - 2022///
SN - 1945-4589
SP - 1128
TI - Work-related stress and well-being in association with epigenetic age acceleration: a Northern Finland Birth Cohort 1966 Study
T2 - Aging
UR - http://dx.doi.org/10.18632/aging.203872
UR - http://hdl.handle.net/10044/1/94887
VL - 14
ER -