Does birth weight predict adult serum cortisol concentrations? Twenty-four-hour profiles in the United Kingdom 1920-1930 Hertfordshire birth cohort

被引:43
作者
Fall, CHD [1 ]
Dennison, E
Cooper, C
Pringle, J
Kellingray, SD
Hindmarsh, P
机构
[1] Univ Southampton, Southampton Gen Hosp, MRC, Environm Epidemiol Unit, Southampton SO16 6YD, Hants, England
[2] Middlesex Hosp, Cobbold Labs, London W1N 8AA, England
关键词
D O I
10.1210/jc.87.5.2001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Low birth weight and weight in infancy are associated with adult insulin resistance and type 2 diabetes. A proposed mechanism is programming of the hypothalamic-pituitary-adrenal axis by intrauterine undernutrition, leading to persistently elevated cortisol concentrations. We examined 24-h serum cortisol profiles (samples every 20 min) in 83 healthy elderly men and women whose birth weight and infant weight were recorded. Variables derived from these profiles included trough, peak, and area under the curve concentrations; the time of onset, rate of rise, duration, and peak of the early morning cortisol rise; postprandial secretion; and regularity of secretion (approximate entropy). None of these parameters was related to birth weight, weight at 1 yr, or change in weight SD score between birth and 1 yr. Consistent with other studies, 0730-0900 h cortisol concentrations were higher in men and women of lower birth weight, although this was not statistically significant (P = 0.08). Our findings do not support the hypothesis that reduced intrauterine and infant growth are associated with continuously raised cortisol concentrations in old age. Programmed effects on the hypothalamic-pituitary-adrenal axis may influence reactivity rather than resting secretion.
引用
收藏
页码:2001 / 2007
页数:7
相关论文
共 38 条
[1]  
Barbazanges A, 1996, J NEUROSCI, V16, P3943
[2]  
Barker DJ., 1998, Mothers, babies, and health in later life, V2
[3]   TYPE 2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS, HYPERTENSION AND HYPERLIPEMIA (SYNDROME-X) - RELATION TO REDUCED FETAL GROWTH [J].
BARKER, DJP ;
HALES, CN ;
FALL, CHD ;
OSMOND, C ;
PHIPPS, K ;
CLARK, PMS .
DIABETOLOGIA, 1993, 36 (01) :62-67
[4]  
*BIOS, 2001, BIOS DIAGN PROT CBG
[5]   EFFECTS OF AGE AND GENDER ON PITUITARY-ADRENOCORTICAL RESPONSIVENESS IN HUMANS [J].
BORN, J ;
DITSCHUNEIT, I ;
SCHREIBER, M ;
DODT, C ;
FEHM, HL .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1995, 132 (06) :705-711
[6]   Fetal hypothalamic-pituitary adrenal (HPA) development and activation as a determinant of the timing of birth, and of postnatal disease [J].
Challis, J ;
Sloboda, D ;
Matthews, S ;
Holloway, A ;
Alfaidy, N ;
Howe, D ;
Fraser, M ;
Newnham, J .
ENDOCRINE RESEARCH, 2000, 26 (04) :489-504
[7]   Size at birth and adrenocortical function in childhood [J].
Clark, PM ;
Hindmarsh, PC ;
Shiell, AW ;
Law, CM ;
Honour, JW ;
Barker, DJP .
CLINICAL ENDOCRINOLOGY, 1996, 45 (06) :721-726
[8]   Adrenal steroid hormones in short children born small for gestational age [J].
Dahlgren, J ;
Boguszewski, M ;
Rosberg, S ;
Albertsson-Wikland, K .
CLINICAL ENDOCRINOLOGY, 1998, 49 (03) :353-361
[9]   With aging in humans the activity of the hypothalamus-pituitary-adrenal system increases and its diurnal amplitude flattens [J].
Deuschle, M ;
Gotthardt, U ;
Schweiger, U ;
Weber, B ;
Korner, A ;
Schmider, J ;
Standhardt, H ;
Lammers, CH ;
Heuser, I .
LIFE SCIENCES, 1997, 61 (22) :2239-2246
[10]   Programming of growth hormone secretion and bone mineral density in elderly men: A hypothesis [J].
Fall, C ;
Hindmarsh, P ;
Dennison, E ;
Kellingray, S ;
Barker, D ;
Cooper, C .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (01) :135-139