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Elderly subjects show severe impairment of dehydroepiandrosterone sulphate and reduced sensitivity of cortisol and aldosterone response to the stimulatory effect of ACTH(1-24)
Authors:Giordano R  Di Vito L  Lanfranco F  Broglio F  Benso A  Gianotti L  Grottoli S  Ghigo E  Arvat E
Institution:Division of Endocrinology, Department of Internal Medicine, University of Turin, Italy.
Abstract:OBJECTIVE: Hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis in ageing has been reported both in humans and in animals and may be involved in age-related changes in body composition, structure functions and metabolism, as well as in brain ageing. Despite the supposed HPA hyperactivity and its refractoriness to negative glucocorticoid feedback, low levels of dehydroepiandrosterone (DHEA) and its sulphate have been clearly demonstrated in human ageing and may suggest another cause of age-related changes in structure function and metabolism. Thus, our aim was to verify the adrenal responsiveness to various ACTH doses in normal elderly subjects. DESIGN: We studied cortisol (F), aldosterone (A) and DHEA responses to the sequential administration of very low, low and supramaximal ACTH1-24 doses (0.06 microg or 0.5 microg followed by 250 microg ACTH1-24 i.v. at 0 and +60 minutes) in healthy elderly subjects (ES) six females and two males, aged 63-75 years, body mass index (BMI) 22-26 kg/m2]. The results in ES were compared with those recorded in healthy young subjects (YS) (six females and six males, aged 22-34 years, BMI 20-25 kg/m2). RESULTS: Basal DHEA levels in ES were lower (P < 0.05) than in YS, while F and A levels were similar in both groups. DHEA, F and A responses to ACTH were dose-dependent in both groups. In ES, however, DHEA levels showed no response to the 0.06 microg dose, a modest increase after 0.5 microg and a clearer rise after 250 microg ACTH; at any dose, the DHEA response in ES was clearly lower than in YS (P < 0.04). The F responses to 0.5 microg and 250 microg ACTH in ES were similar to those in YS; whereas, in ES, 0.06 microg ACTH elicited a non significant F increase which was significantly lower than in YS (P < 0.05). Similarly, the A responses to the highest ACTH doses were similar in both groups but, in ES, 0.06 microg ACTH elicited no increase in A secretion, which was clearly lower than in YS (P < 0.03). CONCLUSIONS: Normal elderly subjects show severe reduction of DHEA response to a wide range of ACTH doses, in agreement with peculiar impairment of the activity of the adrenal reticularis zone in ageing. In contrast to young adults, elderly subjects also show no cortisol and aldosterone response to a very low ACTH dose. This evidence indicates a reduced sensitivity to ACTH in the fasciculata and glomerulosa zones of the adrenal gland in ageing.
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