Abstract
Context: Studies of how aging attenuates GH secretion are confounded by differences in sex-steroid milieus, abdominal visceral fat mass (AVF), and IGF-I concentrations and limited in interpretability by the use of pharmacological doses of secretagogues. Hypothesis: In a controlled estrogenic milieu, near-physiological secretagogue drive will unmask distinct influences of age, AVF, and IGF-I on GH secretion. Location: The study was conducted at an academic medical center. Subjects: Subjects included 10 healthy pre- (PRE) and 10 postmenopausal (POST) women. Procedure: In a defined estradiol (E2) milieu, we compared GH secretion after submaximal stimulation with GH-releasing peptide (GHRP)-2 (ghrelin analog), GHRH, and L-arginine (an inhibitor of somatostatin outflow). Analysis: We related GH responses to age stratum (dichotomous variable) and AVF and IGF-I concentrations (continuous variables). Results: In the face of comparable concentrations of E2, testosterone, and SHBG: 1) age (P < 0.001) and secretagogue type (P < 0.001) independently determined GH secretion; 2) GH responses in POST subjects were only 26-33% of those in PRE (P ≤ 0.002) across all secretagogues; 3) POST women lost the PRE order of secretagogue potency (GHRP-2 > GHRH = L-arginine); and 4) in the combined cohorts, higher AVF predicted reduced L-arginine-stimulated GH secretion (R2 = 0.46, P = 0.0013), whereas higher IGF-I concentrations forecast increased GHRP-2 and GHRH drive (R 2 ≥ 0.52, P ≤ 0.013). Conclusion: A paradigm of near-physiological secretagogue drive in an E2-clamped milieu unmasks tripartite deficits in peptide-signaling pathways in healthy POST, compared with PRE, women. Post hoc analyses indicate that both greater visceral adiposity and lower IGF-I concentrations mark this triple regulatory defect. Copyright © 2007 by The Endocrine Society.
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CITATION STYLE
Veldhuis, J. D., Cosma, M., Erickson, D., Paulo, R., Mielke, K., Farhy, L. S., & Bowers, C. Y. (2007). Tripartite control of growth hormone secretion in women during controlled estradiol repletion. Journal of Clinical Endocrinology and Metabolism, 92(6), 2336–2345. https://doi.org/10.1210/jc.2007-0043
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