Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with Obesity

Einas H Alkhatib1, Andrew Dauber1,2, Doris Elizabeth Estrada1,2

  • 1Division of Pediatric Endocrinology, Children's National Hospital, Washington, District of Columbia, USA.

Insights

Weekly growth hormone (lonapegsomatropin-tcgd) therapy in a patient with prediabetes caused transient hyperglycemia, necessitating insulin treatment. Close glucose monitoring is crucial for patients on weekly growth hormone, especially those with prediabetes.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Disorders

Background:

  • A 12-year-old male with growth hormone deficiency, prediabetes, and obesity was switched to weekly lonapegsomatropin-tcgd due to poor adherence to daily therapy.
  • He had a history of pituitary hypoplasia and was overweight, with an elevated BMI and prediabetes (HbA1c 6.6%).

Observation:

  • Following the first weekly dose of lonapegsomatropin-tcgd, the patient experienced symptomatic hyperglycemia (serum glucose 500 mg/dL) and polyuria.
  • Diabetic ketoacidosis was ruled out, but hyperglycemia required transient insulin therapy for rapid improvement.

Findings:

  • The rapid onset of severe hyperglycemia, despite a relatively low HbA1c (5.7%), suggests a direct side effect of weekly growth hormone therapy.
  • The patient's hyperglycemia resolved quickly with insulin and discontinuation of weekly growth hormone, supporting the diagnosis of a medication-induced effect.

Implications:

  • Weekly growth hormone therapy, while convenient, can precipitate significant insulin resistance and hyperglycemia in susceptible individuals.
  • Close glucose monitoring is essential for pediatric patients with prediabetes or other risk factors when initiating weekly growth hormone therapy.
  • This case highlights the importance of individualized treatment plans and vigilant monitoring for adverse metabolic effects of growth hormone analogs.
Abstract

Related Concept Videos

Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
306
Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
220
Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
374
Hormones Regulating Blood Glucose01:16

Hormones Regulating Blood Glucose

Insulin is released by beta cells of the pancreas when blood glucose levels are high. It facilitates glucose absorption and utilization in insulin-dependent cells with insulin receptors on their plasma membranes. Insulin promotes glucose uptake by increasing the number of glucose transport proteins in the cell membrane, allowing glucose to enter the cell. As a result, glucose utilization and ATP production are enhanced.
In addition to accelerating glucose uptake and utilization, insulin has...
3.6K
Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

Oral Hypoglycemic Agents: Biguanides and Glitazones

Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
248
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
197