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Original Studies |
Division of Endocrinology, Department of Internal Medicine, University of Turin, 10126 Torino, Italy
Address correspondence and requests for reprints to: Ezio Ghigo, M.D., Divisione di Endocrinologia, Ospedale Molinette, C.so Dogliotti 14, 10126 Torino, Italy. E-mail: camanni{at}pianeta.net
The short ACTH test is widely used in clinical practice for the
diagnosis of adrenal insufficiency. It is classically performed
administering 250.0 µg ACTH(124) although 1.0 µg ACTH dose has
been reported having maximal stimulatory effect on cortisol levels in
normal subjects. We aimed to define the maximal and the minimal
stimulatory ACTH dose on cortisol, aldosterone, and
dehydroepiandrosterone (DHEA) in humans. To this goal, in 12 normal
volunteers (6 males and 6 females; age, 2234 yr; body mass index
2025 kg/m2; body surface 1.61.9 m2), we
studied the dose-response effect of eight ACTH doses (0.01, 0.03, 0.06,
0.125, 0.5, 1.0, 25.0, and 250.0 µg) on cortisol, aldosterone, and
DHEA levels. Each ACTH dose administered at 0 min was followed by a
second ACTH dose of 250.0 µg at +60 min. The cortisol
areas under
response curve (
AUCs) after all ACTH doses, apart from 0.01 µg,
were significantly higher (P < 0.02) than that after
placebo, showing a clear dose-response relationship (P
< 0.001). The doses of 0.03 and 1.0 µg ACTH were the minimal and
maximal effective doses, respectively. The cortisol response to 250.0
µg ACTH was not modified by pretreatment with 0.01, 0.03, and 0.06
µg ACTH doses, whereas it was progressively reduced by increasing the
dose of ACTH pretreatment (P < 0.001). The aldosterone
AUCs to all but 0.01 µg ACTH doses were significantly higher
(P < 0.02) than that after placebo, showing a clear
dose-response relationship (P < 0.001). The dose of
0.03 µg was the minimal effective stimulating dose, whereas 25.0 µg
showed the same aldosterone-releasing effect of 250.0 µg. The
aldosterone response to 250.0 µg ACTH, preceeded by placebo, was not
modified by pretreatment with 0.01 and 0.03 µg ACTH doses, whereas it
was reduced by increasing the dose of ACTH pretreatment
(P < 0.050.02). The DHEA
AUCs to all ACTH doses
were significantly higher (P < 0.01) than that after
placebo, showing a clear dose-response relationship (P
< 0.001). The doses of 0.01 and 1.0 µg ACTH were the minimal and
maximal effective dose, respectively. The DHEA response to 250.0 µg
ACTH was not modified by pretreatment with 0.01, 0.03, 0.06, and 0.125
µg ACTH doses, whereas it was progressively reduced by pretreatment
with 0.5, 1.0, and 25.0 µg ACTH doses (P < 0.01). In
conclusion, these results show that an extremely low ACTH dose is
needed to stimulate adrenal steroids and, among them, DHEA seems the
most sensitive to corticotropin stimulation.
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