growth%20hormone%20deficiency
GROWTH HORMONE DEFICIENCY
Growth hormone deficiency in adults reflects an absence of two hormones, growth hormone and insulin-like growth factor-1 (IGF-1), affecting the process of glucose-insulin metabolism, lipolysis and bone remodelling.
History may show pituitary adenoma, surgery &/or radiation treatment of pituitary adenomas or cranial radiation for other disorders, deficiency of other pituitary hormones that may occur concurrently with growth hormone deficiency, and previous childhood growth hormone deficiency.
Physical exam reveals reduced lean body mass with increased weight, body fat predominantly in the abdominal region, thin & dry skin, cool peripheries, poor venous access and blunt affect.

Growth%20hormone%20deficiency Signs and Symptoms

Definition

  • Growth hormone deficiency is a congenital or an acquired growth hormone (GH) axis disruption in the higher brain, hypothalamus or pituitary which results in short stature
  • May occur at any age

Signs and Symptoms

Children
  • Short stature
  • Severely decreased height velocity
  • Hypoglycemia or prolonged jaundice in the neonate

Adults

  • Growth hormone deficiency (GHD) syndrome
    • Decreased lean body mass and increased fat mass
    • Dyslipidemia, insulin resistance, vascular endothelial dysfunction
    • Reduced left ventricular mass, impaired systolic function
    • Reduced sweating
    • Impaired quality of life
  • Other clinical manifestations:
    • Lack of vigor
    • Emotional lability (eg depressed mood/affect)
    • Feeling of social isolation
    • Decreased exercise capacity
    • Reduced bone density and increased risk of fracture, osteopenia

Etiology

Adults

  • Growth hormone deficiency (GHD) in adults reflects an absence of 2 hormones, GH and insulin-like growth factor-1 (IGF-1), affecting the process of glucose-insulin metabolism, lipolysis and bone remodelling
  • Either adult-onset GHD (AOGHD) or childhood-onset (COGHD) and may occur as either isolated GHD or as multiple hormone deficiencies

Children

  • GHD in children reflects a congenital or an acquired GH axis disruption in the higher brain, hypothalamus or pituitary which results in short stature
  • Mainly idiopathic and usually identified because of growth failure
  • Exclude other causes of growth failure using appropriate tests
    • Eg hypothyroidism, chronic systemic diseases, skeletal diseases and Turner syndrome
  • Diagnose GH deficiency based on an integration of all results obtained from physical exam, radiological procedures and lab tests
  • In idiopathic isolated GHD of childhood (hypothalamic GHD), an insulin tolerance test (ITT) or glucagon stimulation tests are recommended
Digital Edition
Asia's trusted medical magazine for healthcare professionals. Get your MIMS Endocrinology - Malaysia digital copy today!
Sign In To Download
Editor's Recommendations
Most Read Articles
29 Jun 2020
At the Novartis-sponsored VERIFY Soft Launch held at Le Meridien, Kuala Lumpur, two distinguished speakers spoke on the latest updates in glucose-lowering therapy and the benefit of early treatment intensification using combination therapy (ie, vildagliptin/metformin) in the management of T2DM.