Growth Hormone Deficiency after Treatment of Acromegaly: A Randomized, Placebo-Controlled Study of Growth Hormone Replacement
Authors:
Open Access
- 1 February 2010
- journal article
- research article
- Published by The Endocrine Society in The Journal of Clinical Endocrinology & Metabolism
- Vol. 95 (2) , 567-577
Abstract
Context: The effects of GH replacement therapy in patients who develop GH deficiency (GHD) after cure of acromegaly have not been established in a placebo-controlled study. Objective: The objective of the study was to determine whether GH replacement improves body composition, cardiovascular risk markers and quality of life in patients with GHD and prior acromegaly. Design: This was a 6-month, randomized, placebo-controlled study. Setting: The study was conducted at a clinical translational science center. Study Participants: Participants included 30 subjects with prior acromegaly and current GHD. Intervention: Interventions included GH or placebo. Main Outcome Measures: Body composition (dual-energy x-ray absorptiometry and cross-sectional computed tomography at L4), cardiovascular risk markers (high-sensitivity C-reactive protein (hsCRP), total, high-density lipoprotein and low-density lipoprotein cholesterol, fibrinogen, and carotid intimal-medial thickness), and quality of life were measured. Results: The mean GH dose at 6 months was 0.58 ± 0.26 mg/d. Total fat mass, visceral adipose tissue (−15.3 ± 18.6 vs. 1.3 ± 12.5%, P = 0.01), and total abdominal fat decreased, and fat-free mass increased, in the GH vs. placebo group. Mean hsCRP levels decreased, but there was no GH effect on other cardiovascular risk markers. There was no change in glycosylated hemoglobin or homeostasis model assessment insulin resistance index. Quality of life improved with GH. Side effects were minimal. Conclusions: This is the first randomized, placebo-controlled study of the effects of GH replacement therapy on body composition and cardiovascular end points in patients who have developed GH deficiency after treatment for acromegaly, a disease complicated by metabolic and body composition alterations and increased cardiovascular risk. GH replacement decreased visceral adipose tissue, increased fat-free mass, decreased hsCRP, and improved quality of life in patients with GHD after cure of acromegaly, with minimal side effects and without an increase in insulin resistance.Keywords
This publication has 63 references indexed in Scilit:
- Limited effects of growth hormone replacement in patients with GH deficiency during long-term cure of acromegalyPituitary, 2009
- Which Patients Do Not Require a GH Stimulation Test for the Diagnosis of Adult GH Deficiency?The Journal of Clinical Endocrinology & Metabolism, 2002
- Growth hormone deficiency and replacement in hypopituitary patients previously treated for acromegaly or Cushing's diseaseEuropean Journal of Endocrinology, 2002
- Inflammatory Cardiovascular Risk Markers in Women with HypopituitarismThe Journal of Clinical Endocrinology & Metabolism, 2001
- Increased arterial intima‐media thickness by B‐M mode echodoppler ultrasonography in acromegalyClinical Endocrinology, 2001
- Treatment of obesity: need to focus on high risk abdominally obese patientsBMJ, 2001
- The diagnosis of growth hormone deficiency (GHD) in successfully treated acromegalic patientsClinical Endocrinology, 2001
- Long-Term Follow-Up Results of Postoperative Radiotherapy in 36 Patients with AcromegalyThe Journal of Clinical Endocrinology & Metabolism, 2000
- Quantitative Insulin Sensitivity Check Index: A Simple, Accurate Method for Assessing Insulin Sensitivity In HumansThe Journal of Clinical Endocrinology & Metabolism, 2000
- Homeostasis model assessment closely mirrors the glucose clamp technique in the assessment of insulin sensitivity: studies in subjects with various degrees of glucose tolerance and insulin sensitivity.Diabetes Care, 2000