Titration of Basal and Prandial Insulin Doses With the Initiation of Glucagon-Like Peptide-1 Receptor Agonist Therapy
Alexander C Hill, Prasanna Santhanam, Caroline B Samples, Roberto Mitsui Akagi, Tariq Latif, Rodhan Khthir

TL;DR
This study found that starting GLP-1 RA therapy in type 2 diabetes patients led to significant improvements in blood sugar control and weight loss, with a trend toward reduced insulin use.
Contribution
The study provides real-world evidence on insulin dose adjustments when initiating GLP-1 RA therapy in type 2 diabetes patients.
Findings
Average hemoglobin A1c decreased significantly from 8.8% to 8.0% after three months of GLP-1 RA therapy.
Patients experienced significant reductions in body weight, LDL cholesterol, and total cholesterol.
Basal and prandial insulin doses decreased, but the changes were not statistically significant.
Abstract
Objective Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have demonstrated significant efficacy in improving glycemic control in type 2 diabetes mellitus, which often results in decreased insulin dose requirements. The purpose of this study was to examine the changes in basal and prandial insulin dose requirements from baseline to three months following initiation of a GLP-1 RA. Methodology A retrospective chart review was conducted of adult insulin-treated patients at the Chertow Diabetes Center, Huntington, WV, who were started on GLP-1 RAs for 24 months. Results Mean daily basal insulin doses decreased by 8.7 units (P = 0.29; mean 8.3% change) and mean daily prandial insulin doses decreased by 9.4 units (P = 0.10; mean 18.4% change) from baseline to three months after starting a GLP-1 RA. Average hemoglobin A1c significantly decreased from 8.8% (73 mmol/mol) at baseline…
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Taxonomy
TopicsDiabetes Treatment and Management · Diabetes Management and Research · Pancreatic function and diabetes
