Cortisol, DHEAS, their ratio and the metabolic syndrome: evidence from the Vietnam Experience Study

Anna Phillips, Douglas Carroll, C Gale, Janet Lord, Wiebke Arlt, G Batty

Research output: Contribution to journalArticle

35 Citations (Scopus)
181 Downloads (Pure)

Abstract

Objectives: The aim of these analyses was to examine the association of cortisol, dehydroepiandrosterone-sulphate (DHEAS), and the cortisol:DHEAS ratio with the Metabolic Syndrome (MetS) and its components. Design: The analyses were cross-sectional. Methods: Participants were 4255 Vietnam era US army veterans. From military service files, telephone interviews, and a medical examination, occupational, socio-demographic, and health data were collected. MetS was ascertained from data on: body mass index; fasting blood glucose or a diabetes medication; blood pressure or a diagnosis of hypertension; HDL cholesterol; and triglyceride levels. Contemporary morning fasted cortisol and DHEAS concentrations were determined. The outcomes were MetS and its components. Analysis was by logistic regression, first adjusting for age and then additionally for an array of candidate confounders. Results: Cortisol, although not in the fully adjusted analysis, and DHEAS were both related to MetS. Whereas high cortisol concentrations were associated with an increased risk of MetS, high DHEAS concentrations appeared protective. By far the strongest associations with MetS were observed for the cortisol:DHEAS ratio; the higher the ratio the greater the risk of having MetS. The ratio was also significantly related to four of the five MetS components. Conclusions: The cortisol:DHEAS ratio is positively associated with MetS. Prospective analyses are needed to help untangle direction of causality, but this study suggests that the cortisol:DHEAS ratio is worthy of further study in this and other health contexts.
Original languageEnglish
Pages (from-to)919-923
Number of pages5
JournalEuropean Journal of Endocrinology
Volume162
Issue number5
DOIs
Publication statusPublished - 1 May 2010

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