Continuous Glucose Monitoring Profiles in Children Receiving High-Dose Glucocorticoid Treatment

Mari Lukka1,2, Vallo Tillmann3,4, Aleksandr Peet3,4

  • 1Department of Paediatrics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia, mari.lukka@kliinikum.ee.

Insights

Two-thirds of pediatric patients on high-dose glucocorticoids (GC) developed hyperglycemia. Continuous glucose monitoring revealed elevated glucose levels, particularly in the evening, highlighting the need for vigilant screening during GC therapy.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Disorders
  • Pharmacology

Background:

  • Glucocorticoids (GC) are primary treatments for various autoimmune and inflammatory conditions.
  • The prevalence and glycemic patterns of GC-induced hyperglycemia (GIH) in children are not well-established.
  • Current guidelines lack specific recommendations for glucose monitoring during high-dose GC therapy.

Purpose of the Study:

  • To characterize glycemic patterns in pediatric patients receiving high-dose systemic GC using continuous glucose monitoring (CGM).
  • To identify risk factors associated with glucocorticoid-induced hyperglycemia (GIH) in this population.

Main Methods:

  • Prospective observational study involving 10 pediatric patients treated with GC (≥1 mg/kg/day prednisolone-equivalent).
  • Continuous glucose monitoring (CGM) was employed during the GC treatment course.
  • Analysis included time in range (TIR), time above range (TAR), and mean sensor glucose (SG).

Main Results:

  • Seven out of ten patients (70%) experienced GIH (SG > 10 mmol/L).
  • Patients with GIH averaged 1.5 hours/day with glucose > 10 mmol/L (TAR: 6% ± 9%).
  • Peak glucose levels were observed between 16:00-23:00, irrespective of GC administration route.

Conclusions:

  • A significant proportion of pediatric patients (two-thirds) develop GIH during high-dose GC therapy.
  • Hyperglycemic episodes occurred regardless of GC administration route (oral or intravenous).
  • Evening hours show higher glucose levels, suggesting this period is critical for GIH screening.
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...
Hyperglycemia01:29

Hyperglycemia

Hyperglycemia is an abnormally high blood glucose level. It is diagnosed by fasting glucose ≥126 mg/dL, 2-hour oral glucose tolerance test (or OGTT) ≥200 mg/dL, random glucose ≥200 mg/dL with symptoms, or HbA1c ≥6.5%. However, HbA1c results may be unreliable in certain conditions, such as anemia or hemoglobinopathies, and the diagnosis should be confirmed unless classic symptoms are present. Postprandial hyperglycemia is typically considered significant when glucose levels exceed 180 mg/dL two...
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...
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses a challenge in...
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
Glucose Homeostasis: Regulation of Blood Glucose01:02

Glucose Homeostasis: Regulation of Blood Glucose

Carbohydrates consumed through foods are converted into glucose, a crucial energy source for the body. In the prandial state, high blood glucose levels stimulate the secretion of insulin from the pancreas. Insulin inhibits hepatic glucose production and stimulates glucose uptake and metabolism by muscle and adipose tissue. The excess glucose is converted into glycogen and stored in the liver and muscles.
During fasting, when blood glucose levels are low, the pancreas secretes glucagon. it...