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  3. Sociodemographic, behavioral and genetic determinants of allostatic load in a Swiss population-based study.
 

Sociodemographic, behavioral and genetic determinants of allostatic load in a Swiss population-based study.

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BORIS DOI
10.7892/boris.78886
Publisher DOI
10.1016/j.psyneuen.2016.02.003
PubMed ID
26881833
Description
Allostatic load (AL) is a marker of physiological dysregulation which reflects exposure to chronic stress. High AL has been related to poorer health outcomes including mortality. We examine here the association of socioeconomic and lifestyle factors with AL. Additionally, we investigate the extent to which AL is genetically determined. We included 803 participants (52% women, mean age 48±16years) from a population and family-based Swiss study. We computed an AL index aggregating 14 markers from cardiovascular, metabolic, lipidic, oxidative, hypothalamus-pituitary-adrenal and inflammatory homeostatic axes. Education and occupational position were used as indicators of socioeconomic status. Marital status, stress, alcohol intake, smoking, dietary patterns and physical activity were considered as lifestyle factors. Heritability of AL was estimated by maximum likelihood. Women with a low occupational position had higher AL (low vs. high OR=3.99, 95%CI [1.22;13.05]), while the opposite was observed for men (middle vs. high OR=0.48, 95%CI [0.23;0.99]). Education tended to be inversely associated with AL in both sexes(low vs. high OR=3.54, 95%CI [1.69;7.4]/OR=1.59, 95%CI [0.88;2.90] in women/men). Heavy drinking men as well as women abstaining from alcohol had higher AL than moderate drinkers. Physical activity was protective against AL while high salt intake was related to increased AL risk. The heritability of AL was estimated to be 29.5% ±7.9%. Our results suggest that generalized physiological dysregulation, as measured by AL, is determined by both environmental and genetic factors. The genetic contribution to AL remains modest when compared to the environmental component, which explains approximately 70% of the phenotypic variance.
Date of Publication
2016-05
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
Allostatic load
•
heritability
•
physiological dysregulation
•
population-based
•
socioeconomic status
Language(s)
en
Contributor(s)
Petrovic, Dusan
Pivin, Edward
Ponte, Belen
Dhayat, Nasserorcid-logo
Universitätsklinik für Nephrologie, Hypertonie und Klinische Pharmakologie
Departement Klinische Forschung, Forschungsgruppe Nephrologie / Hypertonie
Pruijm, Menno
Ehret, Georg
Ackermann, Danielorcid-logo
Universitätsklinik für Nephrologie, Hypertonie und Klinische Pharmakologie
Departement Klinische Forschung, Forschungsgruppe Nephrologie / Hypertonie
Guessous, Idris
Younes, Sandrine Estoppey
Pechère-Bertschi, Antoinette
Vogt, Bruno
Departement Klinische Forschung, Forschungsgruppe Nephrologie / Hypertonie
Universitätsklinik für Nephrologie, Hypertonie und Klinische Pharmakologie
Mohaupt, Markus
Universitätsklinik für Nephrologie, Hypertonie und Klinische Pharmakologie
Departement Klinische Forschung, Forschungsgruppe Nephrologie / Hypertonie
Martin, Pierre-Yves
Paccaud, Fred
Burnier, Michel
Bochud, Murielle
Stringhini, Silvia
Additional Credits
Universitätsklinik für Nephrologie, Hypertonie und Klinische Pharmakologie
Departement Klinische Forschung, Forschungsgruppe Nephrologie / Hypertonie
Series
Psychoneuroendocrinology
Publisher
Elsevier
ISSN
0306-4530
Access(Rights)
open.access
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