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Growth hormone deficiency in Cushing's syndrome: an update on diagnosis and management
1Neuroendocrine Unit and Neuroendocrine and Pituitary Tumor Clinical Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Insights
Growth hormone deficiency (GHD) is common in patients with Cushing's syndrome (CS) in remission. Growth hormone replacement therapy can improve outcomes in children and adults, but requires careful monitoring.
Area of Science:
- Endocrinology
- Metabolic Disorders
Background:
- Endogenous Cushing's syndrome (CS) leads to significant health issues and mortality.
- Growth hormone deficiency (GHD) is a frequent comorbidity in patients with CS, persisting even after remission.
Purpose of the Study:
- To review the epidemiology, mechanisms, and clinical aspects of GHD in patients with CS in remission.
- To discuss GHD diagnosis and the efficacy and safety of growth hormone replacement therapy.
Main Methods:
- Systematic electronic literature search (PubMed) up to July 2025.
- Review focused on patients with Cushing's disease (pituitary CS).
Main Results:
- GHD is prevalent in active CS and can persist in remission.
- In children, GHD causes decreased linear growth. In adults, GHD is linked to increased cardiometabolic burden, reduced muscle strength, lower bone density, and higher fracture rates.
- Growth hormone replacement in children improves adult height; in adults, it may enhance quality of life, bone density, muscle strength, and lipid profiles, with a risk of hyperglycemia.
Conclusions:
- GHD is a significant concern for patients with CS in remission.
- Growth hormone replacement is beneficial for both pediatric and adult patients in remission, necessitating careful monitoring for potential side effects like hyperglycemia.
Introduction:
Endogenous Cushing's syndrome (CS) is associated with substantial morbidity and mortality. Patients in remission may experience many comorbidities, including growth hormone deficiency (GHD).
Areas Covered:
Electronic searches (PubMed) were conducted through July 2025. The published data largely pertain to patients with Cushing's disease (CS caused by a pituitary tumor). This article reviews the epidemiology of GHD in patients with CS in remission, underlying mechanisms, and clinical manifestations. The diagnosis of GHD is discussed along with data on the effectiveness and safety of growth hormone replacement.
Expert Opinion:
GHD is common in patients with active CS and may persist among patients in remission. In children, decreased linear growth is prevalent. In adults in remission, GHD has been associated with a higher prevalence of cardiometabolic burden (hypertension, diabetes mellitus, cardiovascular and cerebrovascular disease), decreased muscle strength, lower bone mineral density and increased prevalence of fractures. The diagnosis of GHD generally requires stimulation testing and should only be undertaken in patients in remission. In children with CS in remission, growth hormone replacement improves adult height. In adults, growth hormone replacement may improve quality of life, bone mineral density, muscle strength and dyslipidemia but requires careful monitoring for the possible development of hyperglycemia.
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