Serum cortisol but not oxidative stress biomarkers are related to frailty: results of a cross-sectional study in Spanish older adults.


Journal

Journal of toxicology and environmental health. Part A
ISSN: 1528-7394
Titre abrégé: J Toxicol Environ Health A
Pays: England
ID NLM: 100960995

Informations de publication

Date de publication:
2019
Historique:
pubmed: 14 8 2019
medline: 22 5 2020
entrez: 14 8 2019
Statut: ppublish

Résumé

Frailty is a multidimensional geriatric syndrome of loss of reserves and increased vulnerability to negative health outcomes. Cortisol, the major hormone of the hypothalamic pituitary adrenal (HPA) axis, and oxidative stress may be influenced by multiple endogenous and environmental factors throughout the lifespan, triggering changes in organism functioning. Association of elevated levels of cortisol and oxidative stress biomarkers with aging and several age-related diseases is well documented. However, the possible role of these factors on frailty status in older adults has not been extensively studied. Hence, the aim of this study was to conduct a cross-sectional study in 252 older adults (≥65 years old) classified according to their frailty status. Plasma cortisol and biomarkers related to oxidative stress including reactive oxygen/nitrogen species, oxidative DNA damage, and total antioxidant capacity were determined in non-frail, pre-frail, and frail subjects. Results showed significantly increasing cortisol concentrations with frailty burden, but no marked association between any oxidative stress biomarker and frailty status. In addition, dependence on activities of daily living and 10-year mortality risk were also correlated with elevated cortisol levels. Current results support the hypothesis that age-related HPA axis dysregulation is associated with frailty status, although further research is necessary to establish the role of cortisol in the pathophysiology of frailty.

Identifiants

pubmed: 31405343
doi: 10.1080/15287394.2019.1654639
doi:

Substances chimiques

Biomarkers 0
Hydrocortisone WI4X0X7BPJ

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

815-825

Auteurs

Diego Marcos-Pérez (D)

Department of Psychology, Area of Psychobiology, Faculty of Education Sciences, Universidade da Coruña, DICOMOSA Group , Coruña , Spain.
Department of Cell and Molecular Biology, Faculty of Sciences, Universidade da Coruña , Coruña , Spain.

María Sánchez-Flores (M)

Department of Psychology, Area of Psychobiology, Faculty of Education Sciences, Universidade da Coruña, DICOMOSA Group , Coruña , Spain.
Department of Cell and Molecular Biology, Faculty of Sciences, Universidade da Coruña , Coruña , Spain.

Ana Maseda (A)

Universidade da Coruña, Gerontology Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Complexo Hospitalario Universitario de A Coruña (CHUAC) , Coruña , Spain.

Laura Lorenzo-López (L)

Universidade da Coruña, Gerontology Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Complexo Hospitalario Universitario de A Coruña (CHUAC) , Coruña , Spain.

José C Millán-Calenti (JC)

Universidade da Coruña, Gerontology Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Complexo Hospitalario Universitario de A Coruña (CHUAC) , Coruña , Spain.

Eduardo Pásaro (E)

Department of Psychology, Area of Psychobiology, Faculty of Education Sciences, Universidade da Coruña, DICOMOSA Group , Coruña , Spain.

Blanca Laffon (B)

Department of Psychology, Area of Psychobiology, Faculty of Education Sciences, Universidade da Coruña, DICOMOSA Group , Coruña , Spain.

Vanessa Valdiglesias (V)

Department of Psychology, Area of Psychobiology, Faculty of Education Sciences, Universidade da Coruña, DICOMOSA Group , Coruña , Spain.

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Classifications MeSH