Morning plasma cortisol as a cardiovascular risk factor: findings from prospective cohort and Mendelian randomization studies.


Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 05 03 2019
accepted: 18 07 2019
pubmed: 22 7 2019
medline: 6 2 2020
entrez: 21 7 2019
Statut: ppublish

Résumé

The identification of new causal risk factors has the potential to improve cardiovascular disease (CVD) risk prediction and the development of new treatments to reduce CVD deaths. In the general population, we sought to determine whether cortisol is a causal risk factor for CVD and coronary heart disease (CHD). Three approaches were adopted to investigate the association between cortisol and CVD/CHD. First, we used multivariable regression in two prospective nested case-control studies (total 798 participants, 313 incident CVD/CHD with complete data). Second, a random-effects meta-analysis of these data and previously published prospective associations was performed (total 6680 controls, 696 incident CVD/CHD). Finally, one- and two-sample Mendelian randomization analyses were performed (122,737 CHD cases, 547,261 controls for two-sample analyses). In the two prospective nested case-control studies, logistic regression adjusting for sex, age, BMI, smoking and time of sampling, demonstrated a positive association between morning plasma cortisol and incident CVD (OR: 1.28 per 1 SD higher cortisol, 95% CI: 1.06-1.54). In the meta-analysis of prospective studies, the equivalent result was OR: 1.18, 95% CI: 1.06-1.31. Results from the two-sample Mendelian randomization were consistent with these positive associations: OR: 1.06, 95% CI: 0.98-1.15. All three approaches demonstrated a positive association between morning plasma cortisol and incident CVD. Together, these findings suggest that elevated morning cortisol is a causal risk factor for CVD. The current data suggest strategies targeted at lowering cortisol action should be evaluated for their effects on CVD.

Identifiants

pubmed: 31325907
doi: 10.1530/EJE-19-0161
pii: EJE-19-0161.R1
pmc: PMC6733337
doi:
pii:

Substances chimiques

Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

429-438

Subventions

Organisme : Medical Research Council
ID : MC_PC_19009
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : CZB/4/733
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12013/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00011/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_15018
Pays : United Kingdom
Organisme : Medical Research Council
ID : G9815508
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 202802/Z/16/Z
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/11/4/28734
Pays : United Kingdom

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Auteurs

Andrew A Crawford (AA)

BHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.

Stefan Soderberg (S)

Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.

Clemens Kirschbaum (C)

Department of Psychology, Dresden University of Technology, Dresden, Germany.

Lee Murphy (L)

Edinburgh Clinical Research Facility, University of Edinburgh, Edinburgh, UK.

Mats Eliasson (M)

Department of Public Health and Clinical Medicine, Sunderby Research Unit, Umeå University, Umeå, Sweden.

Shah Ebrahim (S)

Department of Epidemiology & Population Health, London School of Hygiene & Tropical Medicine, London, UK.

George Davey Smith (G)

MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.

Tommy Olsson (T)

Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.

Naveed Sattar (N)

Division of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

Debbie A Lawlor (DA)

MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.

Nicolas J Timpson (NJ)

MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.

Rebecca M Reynolds (RM)

BHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.

Brian R Walker (BR)

BHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.

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