OBJECTIVE: To assess the effects of the administration of exogenous ghrelin, a peptide with potent GH-releasing activity and glucose-enhancing and insulin-lowering properties, in obese patients with polycystic ovary syndrome (PCOS). DESIGN: Prospective, controlled study. SETTING: Academic research environment. PATIENT(S): Twenty obese women with PCOS, and 15 obese controls. INTERVENTION(S): Oral glucose tolerance test (OGTT) and ghrelin test (1 microg/kg i.v. bolus). MAIN OUTCOME MEASURE(S): Basal hormonal assays, including ghrelin, were performed. Glucose, insulin, and C-peptide were assessed in a fasting condition and during the OGTT. Growth hormone, insulin, and glucose were measured basally and every 15 minutes for 90 minutes after the injection of ghrelin. RESULT(S): Both groups showed an insulin response to the glucose load above the normal range. Significantly lower levels of ghrelin were detected in patients with PCOS compared to controls (108.96 +/- 27.65 Fmol/mL versus 162.47 +/- 42.23 Fmol/mL). Administration of ghrelin markedly enhanced GH levels in both groups (1,888.59 +/- 1,209.53 ng/mL and 1,639.95 +/- 631.79 ng/mL per 90 minutes as GH area under the curve, respectively), with a peak occurring 30 minutes after injection. Ghrelin also induced a trend toward an increase in plasma glucose levels, and a significant decrease in insulin concentrations in both groups. CONCLUSION(S): The injection of ghrelin seems to override the GH secretion defect in obese women with PCOS, and to induce glucoinsulinemic changes in both controls and obese patients with PCOS.
OBJECTIVE: To assess the effects of the administration of exogenous ghrelin, a peptide with potent GH-releasing activity and glucose-enhancing and insulin-lowering properties, in obesepatients with polycystic ovary syndrome (PCOS). DESIGN: Prospective, controlled study. SETTING: Academic research environment. PATIENT(S): Twenty obesewomen with PCOS, and 15 obese controls. INTERVENTION(S): Oral glucose tolerance test (OGTT) and ghrelin test (1 microg/kg i.v. bolus). MAIN OUTCOME MEASURE(S): Basal hormonal assays, including ghrelin, were performed. Glucose, insulin, and C-peptide were assessed in a fasting condition and during the OGTT. Growth hormone, insulin, and glucose were measured basally and every 15 minutes for 90 minutes after the injection of ghrelin. RESULT(S): Both groups showed an insulin response to the glucose load above the normal range. Significantly lower levels of ghrelin were detected in patients with PCOS compared to controls (108.96 +/- 27.65 Fmol/mL versus 162.47 +/- 42.23 Fmol/mL). Administration of ghrelin markedly enhanced GH levels in both groups (1,888.59 +/- 1,209.53 ng/mL and 1,639.95 +/- 631.79 ng/mL per 90 minutes as GH area under the curve, respectively), with a peak occurring 30 minutes after injection. Ghrelin also induced a trend toward an increase in plasma glucose levels, and a significant decrease in insulin concentrations in both groups. CONCLUSION(S): The injection of ghrelin seems to override the GH secretion defect in obesewomen with PCOS, and to induce glucoinsulinemic changes in both controls and obesepatients with PCOS.
Authors: C I Messini; K Dafopoulos; N Chalvatzas; P Georgoulias; G Anifandis; I E Messinis Journal: J Endocrinol Invest Date: 2010-06-04 Impact factor: 4.256
Authors: Robyn A Tamboli; Joseph Antoun; Reem M Sidani; Austin Clements; Emily E Harmata; Pam Marks-Shulman; Bruce D Gaylinn; Brandon Williams; Ronald H Clements; Vance L Albaugh; Naji N Abumrad Journal: Diabetes Obes Metab Date: 2017-05-31 Impact factor: 6.577
Authors: Margaret C Garin; Samantha F Butts; David B Sarwer; Kelly C Allison; Suneeta Senapati; Anuja Dokras Journal: Endocrine Date: 2016-12-21 Impact factor: 3.633
Authors: Diaa E E Rizk; Hazem A Hassan; Ahmed H Al-Marzouqi; Mohammed Shafiullah; Mohamed A Fahim Journal: Int Urogynecol J Pelvic Floor Dysfunct Date: 2008-05-22
Authors: T D Müller; R Nogueiras; M L Andermann; Z B Andrews; S D Anker; J Argente; R L Batterham; S C Benoit; C Y Bowers; F Broglio; F F Casanueva; D D'Alessio; I Depoortere; A Geliebter; E Ghigo; P A Cole; M Cowley; D E Cummings; A Dagher; S Diano; S L Dickson; C Diéguez; R Granata; H J Grill; K Grove; K M Habegger; K Heppner; M L Heiman; L Holsen; B Holst; A Inui; J O Jansson; H Kirchner; M Korbonits; B Laferrère; C W LeRoux; M Lopez; S Morin; M Nakazato; R Nass; D Perez-Tilve; P T Pfluger; T W Schwartz; R J Seeley; M Sleeman; Y Sun; L Sussel; J Tong; M O Thorner; A J van der Lely; L H T van der Ploeg; J M Zigman; M Kojima; K Kangawa; R G Smith; T Horvath; M H Tschöp Journal: Mol Metab Date: 2015-03-21 Impact factor: 7.422