Adrenocorticotropin and Cortisol Hyperresponsiveness to Hexarelin in Patients with Cushings Disease Bearing a Pituitary Microadenoma, But Not in Those with Macroadenoma1
E. Arvat,
R. Giordano,
J. Ramunni,
G. Arnaldi,
A. Colao,
R. Deghenghi,
G. Lombardi,
F. Mantero,
F. Camanni and
E. Ghigo
Division of Endocrinology, University of Turin, Ancona (G.A.,
F.M.), and Naples (A.C., G.L.), Italy; and Europeptides (R.D.),
Argenteuil, France
Address all correspondence and requests for reprints to: E. Ghigo, M.D., Divisione di Endocrinologia, Ospedale Molinette, C.so Dogliotti 14, 10126 Torino, Italy. E-mail: camanni{at}pianeta.net
We previously reported that in Cushings disease (CD)the ACTH-
and cortisol (F)-releasing activity of Hexarelin (HEX),a GH
secretagogue, is exaggerated with respect to that in normalsubjects
and is higher than that of human CRH (hCRH), but itis absent in
Cushings syndrome. Our aim was to extendthe study about the effects
of HEX (2.0 µg/kg, iv) onACTH and F secretion in 21 patients with CD
(3 men and 18 women,1668 yr old). Based on magnetic resonance
imaging, 15CD patients had pituitary microadenoma, and 6 had
macroadenoma.The results in CD patients were compared with those in 27
normalage-matched controls (NS; 10 men and 17 women, 2469 yrold).
Basal ACTH and F levels in CD were similar in patientswith microadenom
(mean ± SEM, 78.3 ± 7.2 pg/mLand 237.1 ±
23.6 µg/L, respectively) and macroadenoma(57.4 ± 9.0 pg/mL and
196.9 ± 20.1 µg/L,respectively) and were higher
(P < 0.001) than those in NS(17.7 ± 2.0
pg/mL and 115.3 ± 6.7 µg/L,respectively). In microadenoma CD
patients, HEX induced markedACTH and F increases ( peak, mean ±
SEM: 261.2 ±77.6 pg/mL and 226.1 ± 87.2
µg/L, respectively),which were higher (P <
0.04) than those induced by hCRH (45.6± 16.9 pg/mL and 84.6
± 25.7 µg/L, respectively).Moreover, in microadenoma CD patients,
the ACTH and F responsesto HEX were higher (P <
0.001) than those in NS (18.5 ±4.0 pg/mL and 36.1 ± 6.8
µg/L, respectively). Inmacroadenoma CD patients, HEX induced a
slight, but significantincrease (P < 0.02) in
ACTH and F levels (33.9 ± 18.0pg/mL and 89.6 ± 34.3
µg/L, respectively), whichwas not significantly different from that
elicited by hCRH (20.0± 7.0 pg/mL and 54.8 ± 21.3 µg/L,
respectively).In macroadenoma CD patients, the ACTH and F responses to
HEXand hCRH were, in turn, similar to those in NS.
In conclusion, our findings demonstrate that the ACTH and F
hyperresponsivenessto HEX is present in Cushings disease with
micro-, butnot macro- ACTH-secreting pituitary adenoma. This finding
agreeswith other evidence pointing toward differences in the hormonal
behaviorbetween micro- and ACTH-secreting pituitary macroadenomas.
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