Comparison of Diluted Insulin (U10) Versus Standard (U100) Insulin in Automated Insulin Delivery Systems: Reducing

Heidi Falk1, Ada Aaltio1, Mari-Anne Pulkkinen1

  • 1Department of Pediatrics and Adolescence, University of Helsinki and Helsinki University Hospital, Helsinki, Uusimaa, Finland.

Insights

Diluted U10 insulin in automated insulin delivery systems significantly reduced time below range in young children with Type 1 diabetes. This approach improved glycemic control without increasing hyperglycemia, offering a safer treatment option.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Disorders
  • Diabetes Technology

Background:

  • Managing Type 1 diabetes in very young children (CwT1D) presents unique challenges due to their minimal insulin requirements.
  • Automated Insulin Delivery (AID) systems are increasingly used, but require precise insulin dosing.
  • Investigating the efficacy and safety of diluted insulin (U10) in AID systems for CwT1D is crucial.

Purpose of the Study:

  • To evaluate the safety and glycemic outcomes of using diluted U10 insulin versus standard U100 insulin in an AID system for young children with Type 1 diabetes.
  • To compare the time spent in various glucose ranges (TBR) between children using diluted insulin and a control group.

Main Methods:

  • A cohort of 19 children (0-4 years) using diluted U10 insulin in an AID system with a maximum daily dose of ≤6 units was identified.
  • A control group of 27 age- and gender-matched children using standard U100 insulin in an AID system was selected.
  • Continuous Glucose Monitoring (CGM) data were analyzed longitudinally over 12 months to assess time-by-treatment effects.

Main Results:

  • Diluted U10 insulin use led to a significant reduction in time below 3.9 mmol/L and 3.0 mmol/L within 3 months, which was sustained for 12 months.
  • Children using diluted insulin showed lower time below 3.9 mmol/L at later follow-up visits compared to controls.
  • HbA1c-adjusted analysis revealed a significant between-group difference, with diluted insulin users having 1.85% and 1.52% lower time below 3.9 mmol/L at 9 and 12 months, respectively.

Conclusions:

  • Diluted U10 insulin is a safe and effective option for young children with Type 1 diabetes using AID systems who require low insulin doses.
  • This approach successfully reduces time spent in hypoglycemia (low blood glucose) without inducing hyperglycemia.
  • The findings support the use of diluted insulin to optimize glycemic management in this vulnerable pediatric population.
Abstract

Related Concept Videos

Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into rapid-acting...
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...
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
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...
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 manages...
Parenteral Drug Delivery Systems: Injectables, Implants, and Infusion Devices01:28

Parenteral Drug Delivery Systems: Injectables, Implants, and Infusion Devices

Parenteral drug delivery systems play a crucial role in modern therapeutics by enabling the direct administration of drugs into the systemic circulation, bypassing the gastrointestinal tract. These systems are particularly valuable for poorly absorbed oral medications that are unstable in the digestive environment or require rapid onset or sustained therapeutic levels. Delivery is achieved through intravenous, intramuscular, or subcutaneous routes, each selected based on the drug's properties...