TY - JOUR
T1 - The negative association between total ghrelin levels. body mass and insulin secretion is lost in hypercortisolemic patients with Cushing's disease
AU - Giordano, Roberta
AU - Picu, Andrea
AU - Pagotto, Uberto
AU - De Iasio, Rosaria
AU - Bonelli, Lorenza
AU - Prodam, Flavia
AU - Broglio, Fabio
AU - Marafetti, Lisa
AU - Pasquali, Renato
AU - Maccario, Mauro
AU - Ghigo, Ezio
AU - Arvat, Emanuela
PY - 2005/10
Y1 - 2005/10
N2 - Objective: Ghrelin exerts a wide spectrum of endocrine and non-endocrine actions. The stomach is the major source of circulating ghrelin levels that are negatively associated with body mass, insulin and glucose levels. The role of glucocorticoids in ghrelin secretion and action is still unclear. Design: In 8 patients with Cushing's disease (CD, BMI 29.8±1.6 kg/m2), 7 normal (NS) and 6 obese subjects (OB, BMI 32.9±1.1 kg/m2) we studied: a) total ghrelin levels (every 15 min over 3 h) and their correlation with BMI, insulin, glucose, homeostatic model assessment (HOMA) index, ACTH and cortisol levels; b) GH, ACTH, cortisol, insulin and glucose responses to acylated ghrelin administration (1.0 μg/kg i.v. at 0 min). Results: CD patients had BMI, insulin and glucose levels as well as HOMA index higher than those in NS (P < 0.05) but similar to those in OB. Despite this, total ghrelin levels in CD were similar to those in NS and both were higher (P < 0.05) than those in OB. No correlation was found among total ghrelin and BMI, insulin, glucose, ACTH and cortisol levels in CD patients. The GH responses to ghrelin in CD and OB were similar and both were lower (P < 0.002) than those in NS. In CD ghrelin induced exaggerated ACTH and cortisol responses clearly higher (P < 0.005) than in OB and NS. Ghrelin administration increased glucose in all groups; insulin levels showed slight decrease that was significant (P < 0.05) in OB only. Conclusions: Hypercortisolism in humans is associated with impaired ghrelin secretion and action. In fact, total ghrelin secretion in CD is not reduced despite increased BMI, insulin and glucose levels, while the GH and ACTH responses to acylated ghrelin are clearly reduced and enhanced, respectively.
AB - Objective: Ghrelin exerts a wide spectrum of endocrine and non-endocrine actions. The stomach is the major source of circulating ghrelin levels that are negatively associated with body mass, insulin and glucose levels. The role of glucocorticoids in ghrelin secretion and action is still unclear. Design: In 8 patients with Cushing's disease (CD, BMI 29.8±1.6 kg/m2), 7 normal (NS) and 6 obese subjects (OB, BMI 32.9±1.1 kg/m2) we studied: a) total ghrelin levels (every 15 min over 3 h) and their correlation with BMI, insulin, glucose, homeostatic model assessment (HOMA) index, ACTH and cortisol levels; b) GH, ACTH, cortisol, insulin and glucose responses to acylated ghrelin administration (1.0 μg/kg i.v. at 0 min). Results: CD patients had BMI, insulin and glucose levels as well as HOMA index higher than those in NS (P < 0.05) but similar to those in OB. Despite this, total ghrelin levels in CD were similar to those in NS and both were higher (P < 0.05) than those in OB. No correlation was found among total ghrelin and BMI, insulin, glucose, ACTH and cortisol levels in CD patients. The GH responses to ghrelin in CD and OB were similar and both were lower (P < 0.002) than those in NS. In CD ghrelin induced exaggerated ACTH and cortisol responses clearly higher (P < 0.005) than in OB and NS. Ghrelin administration increased glucose in all groups; insulin levels showed slight decrease that was significant (P < 0.05) in OB only. Conclusions: Hypercortisolism in humans is associated with impaired ghrelin secretion and action. In fact, total ghrelin secretion in CD is not reduced despite increased BMI, insulin and glucose levels, while the GH and ACTH responses to acylated ghrelin are clearly reduced and enhanced, respectively.
UR - http://www.scopus.com/inward/record.url?scp=27644466366&partnerID=8YFLogxK
U2 - 10.1530/eje.1.02003
DO - 10.1530/eje.1.02003
M3 - Article
SN - 0804-4643
VL - 153
SP - 535
EP - 543
JO - European Journal of Endocrinology
JF - European Journal of Endocrinology
IS - 4
ER -