Diurnal Cortisol Patterns, Future Diabetes, and Impaired Glucose Metabolism in the Whitehall II Cohort Study

被引:99
作者
Hackett, Ruth A. [1 ]
Kivimaki, Mika [1 ]
Kumari, Meena [2 ]
Steptoe, Andrew [1 ]
机构
[1] UCL, Dept Epidemiol & Publ Hlth, 1-19 Torrington Pl, London WC1E 6BT, England
[2] Univ Essex, Inst Social & Econ Res, Colchester CO4 3SQ, Essex, England
基金
英国经济与社会研究理事会; 英国医学研究理事会; 美国国家卫生研究院;
关键词
11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1; AWAKENING RESPONSE; INSULIN-RESISTANCE; RISK; OBESITY; OVERWEIGHT; SECRETION; MELLITUS; MARKERS; STRESS;
D O I
10.1210/jc.2015-2853
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: The hypothalamic pituitary-adrenal axis is thought to play a role in type 2 diabetes (T2D). However, evidence for an association between cortisol and future glucose disturbance is sparse. Objective: The aim was to examine the association of diurnal cortisol secretion with future T2D and impaired glucose metabolism in a community-dwelling population. Design: This is a prospective cohort study of salivary cortisol measured at the 2002-2004 clinical examination of the Whitehall II study, United Kingdom. We measured cortisol (nmol/l) from six saliva samples obtained over the course of a day: at waking, +30 minutes, +2.5 hours, +8 hours, +12 hours, and bedtime. Participants who were normoglycemic in 2002-2004 (phase 7) were reexamined in 2012-2013 (phase 11). Setting: The occupational cohort was originally recruited in 1985-1988. Participants: A total of 3270 men and women with an average age of 60.85 years at phase 7 (2002-2004). Outcome Measures: Incident T2D and impaired fasting glucose in 2012-2013 were measured. Results: Raised evening cortisol at phase 7 was predictive of new-onset T2D at phase 11 (odds ratio [OR], 1.18; 95% confidence interval [CI], 1.01-1.37) with a trend for a flatter slope in participants with incident T2D (odds ratio, 1.15; 95% CI, 0.99-1.33). When expanding this analysis to a broader category of glucose disturbance we found that a flattened diurnal cortisol slope at phase 7 was predictive of future impaired fasting glucose or T2D at phase 11 (OR, 1.12; 95% CI, 1.02-1.22), as was high bedtime cortisol (OR, 1.10; 95% CI, 1.01-1.20). Conclusions: In this nonclinical population, alterations in diurnal cortisol patterns were predictive of future glucose disturbance.
引用
收藏
页码:619 / 625
页数:7
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