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Injectable semaglutide and reductions in HbA1c and weight in the real world in people switched from alternative glucagon-like peptide-1 receptor agonists
Authors:Thomas S. J. Crabtree  Karen Adamson  Hazel Reid  Dennis Barnes  Siva Sivappriyan  Alex Bickerton  Ian W. Gallen  Benjamin C. T. Field  Iskandar Idris  Robert E. J. Ryder  all ABCD semaglutide audit contributors
Affiliation:1. City Hospital, Sandwell & West Birmingham Hospitals NHS Trust, Birmingham, UK;2. St John's Hospital, Livingston, UK;3. Maidstone and Tunbridge Wells NHS Trust, Kent, UK;4. Yeovil District Hospital NHS Trust, Yeovil, UK;5. Royal Berkshire Hospitals NHS Trust, Reading, UK;6. Department of Clinical & Experimental Medicine, Faculty of Health & Medical Sciences, University of Surrey, Guildford, UK

Surrey & Sussex Healthcare NHS Trust, Guildford, UK;7. School of Medicine, University of Nottingham, Nottingham, UK

Royal Derby Hospital, University Hospitals of Derby and Burton NHS Trust, Derby, UK

Abstract:The ABCD semaglutide audit was designed to capture the routine clinical outcomes of people commenced on semaglutide in the UK. Previous work showed differential reductions in HbA1c and weight dependent on previous glucagon-like peptide-1 receptor agonist (GLP-1RA) exposure. The analysis, in this research letter, shows that decreases in HbA1c and weight associated with semaglutide occur irrespective of previous GLP-1RA use. However, HbA1c reductions were less if switched from dulaglutide or liraglutide and weight changes were attenuated if switched from dulaglutide or exenatide, potentially suggesting differing potencies between GLP-1RAs. Dedicated studies with head-to-head comparisons are needed to confirm these findings.
Keywords:GLP-1 analogue  observational study  type 2 diabetes
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