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Published on: November 16, 2011
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.
Introduction:
A 12-year-and-9-month-old non-Hispanic black male with a history of growth hormone deficiency, pituitary hypoplasia, prediabetes, obesity, hypertension, and hyperlipidemia was initiated on weekly growth hormone (lonapegsomatropin-tcgd) and then transiently developed symptomatic hyperglycemia to 500 mg/dL. We aimed to describe this medication's effect.
Case Presentation:
He was born full term and appropriate for gestational age. He was referred to endocrinology at 3.5 years of age for short stature with a height SDS of -2.48. IGF-1 51.1 ng/mL and IGFBP-3 1.2 ng/mL were low. GH stimulation test noted baseline and peak GH of 0.1 ng/mL. MRI brain showed hypoplastic adenohypophysis, aplastic pituitary stalk, and ectopic neurohypophysis. There had been difficulty with adherence to daily GH over the following 9 years. BMI trajectory rose above 180% of the 95th percentile. By age 12, A1c was 6.6%. Metformin was started and increased to 1,000 mg twice daily. Subsequent A1c was 6.0%. Due to poor compliance with daily GH, at 12 years and 9 months, he was initiated on 22 mg (0.25 mg/kg/week) of weekly lonapegsomatropin-tcgd to improve compliance. The day after his first injection, he developed non-bloody, non-bilious emesis. He denied headaches and endorsed polyuria. Due to concern for increased intracranial pressure, he was sent to the emergency department; however, ophthalmologic exam was negative. Initial serum glucose was 500 mg/dL, then 336 mg/dL after 1-L normal saline. Hemoglobin A1c was 5.7%, urine glucose 3+ mg/dL, and urine ketones 2+ mg/dL. Venous pH of 7.379 and bicarbonate of 20.6 mmol/L ruled out diabetic ketoacidosis. Metformin was held during the hospitalization. Hyperglycemia rapidly improved with transient insulin administration. He received one dose of glargine 20 units. He was initiated on lispro carb ratio of 1:8 and correction factor 1:15 for target glucose 150 mg/dL. By day four, glucoses were below 100 mg/dL; lispro was discontinued, and he was discharged home. Weekly GH was discontinued with plans to resume daily GH therapy in several months.
Conclusion:
Lonapegsomatropin-tcgd offers the convenience of weekly rather than daily GH treatment; however, this patient developed a rapid increase in insulin resistance and hyperglycemia requiring insulin. The discrepancy between the glucose of 500 mg/dL and A1c of 5.7%, along with the rapid resolution of hyperglycemia, is further consistent with a medication side effect. Close glucose monitoring of patients initiated on weekly growth hormone is crucial, particularly in those with a history of prediabetes.
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