Elevated plasma cortisol in glucose-intolerant men: Differences in responses to glucose and habituation to venepuncture

被引:70
作者
Reynolds, RM [1 ]
Walker, BR
Syddall, HE
Whorwood, CB
Wood, PJ
Phillips, DIW
机构
[1] Univ Edinburgh, Western Gen Hosp, Dept Med Sci, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Southampton, MRC, Environm Epidemiol Unit, Southampton SO16 6YD, Hants, England
[3] Southampton Gen Hosp, Reg Endocrine Unit, Southampton SO16 6YD, Hants, England
关键词
D O I
10.1210/jc.86.3.1149
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent evidence suggests that variations in cortisol activity within the physiological range contribute to associations between multiple cardiovascular risk factors. Plasma cortisol measurements during a glucose tolerance test differ in men with hypertension, insulin resistance, and glucose intolerance, but it is unclear whether this reflects altered responses of cortisol to glucose, altered circadian rhythm, or altered habituation to multiple sampling. We performed a single-blind randomized cross-over study comparing 75 g oral glucose with placebo in 39 fasted men (22 glucose intolerant and 17 controls) aged 68-77 yr. In all subjects, plasma cortisol fell during the glucose tolerance test. Subjects with glucose intolerance had significantly higher plasma cortisol following placebo (P = 0.001), suggesting an altered circadian rhythm. Treatment with an oral glucose load blunted the circadian fall in plasma cortisol (P = 0.002), but this response was no different in controls or glucose intolerant subjects. In addition, 0900h plasma cortisol was higher in the first study phase in controls (P = 0.01) but not in glucose-intolerant subjects (P = 0.18), who showed a lack of habituation to repeated plasma measurements. These data support the hypothesis that alterations in central regulation of the hypothalamic-pituitary-adrenal axis may be important in glucose intolerance.
引用
收藏
页码:1149 / 1153
页数:5
相关论文
共 30 条
[1]   FOOD-INDUCED CORTISOL SECRETION IS MEDIATED BY CENTRAL ALPHA-1 ADRENOCEPTOR MODULATION OF PITUITARY ACTH-SECRETION [J].
ALDAMLUJI, S ;
IVESON, T ;
THOMAS, JM ;
PENDLEBURY, DJ ;
REES, LH ;
BESSER, GM .
CLINICAL ENDOCRINOLOGY, 1987, 26 (05) :629-636
[2]   Socioeconomic determinants of health - Stress and the biology of inequality [J].
Brunner, E .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 314 (7092) :1472-1476
[3]   ENHANCED ADRENOCORTICAL ACTIVITY AS A CONTRIBUTING FACTOR TO DIABETES IN HYPERANDROGENIC WOMEN [J].
BUFFINGTON, CK ;
GIVENS, JR ;
KITABCHI, AE .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1994, 43 (05) :584-590
[4]   HYPERCORTISOLISM IN DIABETES-MELLITUS [J].
CAMERON, OG ;
THOMAS, B ;
TIONGCO, D ;
HARIHARAN, M ;
GREDEN, JF .
DIABETES CARE, 1987, 10 (05) :662-664
[5]   METABOLIC EFFECTS OF THE NOCTURNAL RISE IN CORTISOL ON CARBOHYDRATE-METABOLISM IN NORMAL HUMANS [J].
DINNEEN, S ;
ALZAID, A ;
MILES, J ;
RIZZA, R .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (05) :2283-2290
[6]   The relationship of blood pressure with glucose, insulin, heart rate, free fatty acids and plasma cortisol levels according to degree of obesity in middle-aged men [J].
Filipovsky, J ;
Ducimetiere, P ;
Eschwege, E ;
Richard, JL ;
Rosselin, G ;
Claude, JR .
JOURNAL OF HYPERTENSION, 1996, 14 (02) :229-235
[7]   Cortisol effects on body mass, blood pressure, and cholesterol in the general population [J].
Fraser, R ;
Ingram, MC ;
Anderson, NH ;
Morrison, C ;
Davies, E ;
Connell, JMC .
HYPERTENSION, 1999, 33 (06) :1364-1368
[8]   Supraphysiological hyperinsulinemia acutely increases hypothalamic-pituitary-adrenal secretory activity in humans [J].
Fruehwald-Schultes, B ;
Kern, W ;
Bong, W ;
Wellhoener, P ;
Kerner, W ;
Born, J ;
Fehm, HL ;
Peters, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (09) :3041-3046
[9]   Increased salivary cortisol reliably induced by a protein-rich midday meal [J].
Gibson, EL ;
Checkley, S ;
Papadopoulos, A ;
Poon, L ;
Daley, S ;
Wardle, J .
PSYCHOSOMATIC MEDICINE, 1999, 61 (02) :214-224
[10]   FETAL AND INFANT GROWTH AND IMPAIRED GLUCOSE-TOLERANCE AT AGE 64 [J].
HALES, CN ;
BARKER, DJP ;
CLARK, PMS ;
COX, LJ ;
FALL, C ;
OSMOND, C ;
WINTER, PD .
BMJ-BRITISH MEDICAL JOURNAL, 1991, 303 (6809) :1019-1022