Race, cortisol, and subclinical cardiovascular disease in 9- to 11-year-old children.


Journal

Health psychology : official journal of the Division of Health Psychology, American Psychological Association
ISSN: 1930-7810
Titre abrégé: Health Psychol
Pays: United States
ID NLM: 8211523

Informations de publication

Date de publication:
Sep 2023
Historique:
pmc-release: 01 09 2024
medline: 18 8 2023
pubmed: 6 7 2023
entrez: 6 7 2023
Statut: ppublish

Résumé

Non-Hispanic Black Americans have a greater risk for certain subtypes of cardiovascular disease (CVD; e.g., stroke and heart failure) relative to non-Hispanic White Americans. Moreover, Black relative to White adults consistently show elevated cortisol, a CVD risk. The impact of race, environmental stress, and cortisol on subclinical CVD has yet to be fully researched in children. We assessed diurnal salivary cortisol slopes and hair cortisol in a sample of 9- to 11-year-old children ( After adjusting for covariates, we found that Black children had significantly flatter diurnal cortisol slopes, higher hair cortisol, and thicker IMT than White children. Significant pathways were found: race → salivary cortisol slope → cfPWV (effect = -0.059, 95% CI [-0.116, -0.002]) and race → hair cortisol → cIMT (effect = -0.008, [-0.016, -0.002]). Black children also experienced significantly more environmental stress than White children; however, only income inequality served as a significant indirect pathway from race to salivary cortisol (effect = 0.029, [0.003, 0.060]). Relative to White children, Black children had significantly greater hair cortisol and flatter diurnal slopes which, in turn, were associated with greater subclinical CVD. As suggested by a significant indirect pathway, income inequality might partially explain the race-cortisol association. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

Sections du résumé

BACKGROUND BACKGROUND
Non-Hispanic Black Americans have a greater risk for certain subtypes of cardiovascular disease (CVD; e.g., stroke and heart failure) relative to non-Hispanic White Americans. Moreover, Black relative to White adults consistently show elevated cortisol, a CVD risk. The impact of race, environmental stress, and cortisol on subclinical CVD has yet to be fully researched in children.
METHOD METHODS
We assessed diurnal salivary cortisol slopes and hair cortisol in a sample of 9- to 11-year-old children (
RESULTS RESULTS
After adjusting for covariates, we found that Black children had significantly flatter diurnal cortisol slopes, higher hair cortisol, and thicker IMT than White children. Significant pathways were found: race → salivary cortisol slope → cfPWV (effect = -0.059, 95% CI [-0.116, -0.002]) and race → hair cortisol → cIMT (effect = -0.008, [-0.016, -0.002]). Black children also experienced significantly more environmental stress than White children; however, only income inequality served as a significant indirect pathway from race to salivary cortisol (effect = 0.029, [0.003, 0.060]).
CONCLUSIONS CONCLUSIONS
Relative to White children, Black children had significantly greater hair cortisol and flatter diurnal slopes which, in turn, were associated with greater subclinical CVD. As suggested by a significant indirect pathway, income inequality might partially explain the race-cortisol association. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

Identifiants

pubmed: 37410422
pii: 2023-87659-001
doi: 10.1037/hea0001300
pmc: PMC10601363
mid: NIHMS1917472
doi:

Substances chimiques

Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

657-667

Subventions

Organisme : NIEHS NIH HHS
ID : R01 ES023252
Pays : United States
Organisme : NIH HHS
Pays : United States

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Auteurs

Brooks B Gump (BB)

Department of Public Health, Syracuse University.

Bryce Hruska (B)

Department of Public Health, Syracuse University.

Kevin Heffernan (K)

Department of Exercise Science, Syracuse University.

Lynn S Brann (LS)

Department of Nutrition and Food Studies, Syracuse University.

Margaret Voss (M)

Department of Nutrition and Food Studies, Syracuse University.

Charlotte Labrie-Cleary (C)

Department of Chemistry, State University of New York College at Oswego.

Hana Cheng (H)

Department of Chemistry, State University of New York College at Oswego.

James A MacKenzie (JA)

Department of Biological Sciences, State University of New York College at Oswego.

Sarah Woolf-King (S)

Department of Psychology, Syracuse University.

Stephen Maisto (S)

Department of Psychology, Syracuse University.

Kestutis Bendinskas (K)

Department of Chemistry, State University of New York College at Oswego.

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