Glucagonlike Peptide-1 Receptor Imaging in Individuals with Type 2 Diabetes

• Published in: The Journal of nuclear medicine (1978) Vol. 63; no. 5; pp. 794 - 800
• Main Authors: Eriksson, Olof, Velikyan, Irina, Haack, Torsten, Bossart, Martin, Laitinen, Iina, Larsen, Philip J, Berglund, Jan Erik, Antoni, Gunnar, Johansson, Lars, Pierrou, Stefan, Tillner, Joachim, Wagner, Michael
• Format: Journal Article
• Language: English
• Published: United States Society of Nuclear Medicine 01.05.2022
• Subjects: b-cell mass; Clinical Investigation; Diabetes Mellitus, Type 2 - diagnostic imaging; exendin; Gallium Radioisotopes; GLP1R; Glucagon-Like Peptide-1 Receptor - metabolism; Humans; Peptides - chemistry; PET; Positron Emission Tomography Computed Tomography; Positron-Emission Tomography - methods; Reproducibility of Results; type 2 diabetes; GLP1R; exendin; β-cell mass; type 2 diabetes; PET
• ISSN: 0161-5505; 1535-5667; 1535-5667
• DOI: 10.2967/jnumed.121.262506

The glucagonlike peptide-1 receptor (GLP1R) is a gut hormone receptor, intricately linked to regulation of blood glucose homeostasis via several mechanisms. It is an established and emergent drug target in metabolic disease. The PET radioligand Ga-DO3A-VS-exendin4 ( Ga-exendin4) has the potential to enable longitudinal studies of GLP1R in the human pancreas. Ga-exendin4 PET/CT examinations were performed on overweight-to-obese individuals with type 2 diabetes (  = 13) as part of a larger target engagement study (NCT03350191). A scanning protocol was developed to optimize reproducibility (target amount of 0.5 MBq/kg [corresponding to peptide amount of <0.2 µg/kg], blood sampling, and tracer stability assessment). The pancreas and abdominal organs were segmented, and binding was correlated with clinical parameters. Uptake of Ga-exendin4 in the pancreas, but not in other abdominal tissues, was high but variable between individuals. There was no evidence of self-blocking of GLP1R by the tracer in this protocol, despite the high potency of exendin4. The results showed that a full dynamic scan can be simplified to a short static scan, potentially increasing throughput and reducing patient discomfort. The Ga-exendin4 concentration in the pancreas (i.e., GLP1R density) correlated inversely with the age of the individual and tended to correlate positively with body mass index. However, the total GLP1R content in the pancreas did not. In summary, we present an optimized and simplified Ga-exendin4 scanning protocol to enable reproducible imaging of GLP1R in the pancreas. Ga-exendin4 PET may enable quantification of longitudinal changes in pancreatic GLP1R during the development of type 2 diabetes, as well as target engagement studies of novel glucagonlike peptide-1 agonists.