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| Name | Class |
|---|---|
| University of Coimbra | OTHER |
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Validation of the exendin-based beta cell imaging technique in patients with type 2 diabetes
Rationale: Reliable imaging biomarkers for non-invasive characterisation of beta-cell mass (BCM) are needed to aid understanding regarding the relationship between beta-cell mass and function during the course of type 2 diabetes (T2D). This study will provide critical information necessary to validate the applicability of exendin-based imaging techniques in patients with T2D. The characterization of beta-cells is currently limited to pancreatic specimens available at autopsy, as in vivo pancreatic biopsy is associated with complications unacceptable in clinical studies. To date, only measurements of circulating C-peptide and insulin levels can be obtained, but these measures do not reflect beta-cell mass, only total beta-cell function. Reliable imaging biomarkers for non-invasive characterisation of beta cell mass are therefore needed. These biomarkers could also be used to validate novel therapeutic strategies aimed to increase or preserve BCM or identify whether patients are eligible for a certain therapeutic strategy (e.g. when certain amount of beta-cells is required). One can also think of identifying early responders to therapies, to avoid unnecessary drug use and the accompanying costs.
The objective of this study is to determine the specificity of Exendin-4 during the course of T2D and to examine the role of glycemic control on the correlation between pancreatic Exendin-4 uptake, BCM and GLP-1R expression in patients with T2D undergoing (partial) pancreatectomy. This will allow examination of the role of glycemic control on exendin uptake in humans, but also implementation of clinical guidelines for the interpretation of clinical exendin-based scans in patients with T2D to avoid false interpretation of the scans.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 111In-exendin-DTPA | Experimental | Injection of 111In-exendin-DTPA for subsequent localization of the tracer in excised tissue using autoradiography |
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| exendin-IRDye800CW | Experimental | Injection of exendin-4-IRDye800CW for subsequent localization of the tracer in excised tissue using fluorescence microscopy |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 111In-DTPA-exendin-4 | Drug | Injection of 111In-DTPA-exendin-4 and localization of the tracer in excised pancreatic tissue using autoradiography |
|
| Measure | Description | Time Frame |
|---|---|---|
| Pancreatic exendin uptake 111In-DTPA exendin-4 | The pancreatic uptake of 111In-DTPA-exendin-4 will be quantified using ex vivo SPECT | 111In-DTPA-exendin-4 injection will be performed a day before planned surgery, and uptake will be determined using ex vivo SPECTof the resected tissue one day after surgery |
| Pancreatic exendin uptake 111In-DTPA exendin-4 | The pancreatic uptake of 111In-DTPA-exendin-4 will be quantified using tissue autoradiography | 111In-DTPA-exendin-4 injection will be performed a day before planned surgery, and uptake will be determined with tissue autoradiography immediately after resection |
| Beta cell function | The beta cell function will be determined with a glucose tolerance test | The glucose tolerance test will be performed within a week before planned surgery |
| Blood glucose levels | Glycemic control will be determined by monitoring blood glucose levels | Blood glucose levels will be continuously monitored a week prior to surgery |
| HbA1C levels | HbA1C levels will be determined as a measure of glycemic control | HbA1C levels will be determined within a week before planned surgery |
| Pancreatic exendin uptake IRDye800CW-exendin-4 | Uptake of IRDye800CW-exendin4 will be visualized with microscopy | IRDye800CW-exendin-4 injection will be performed a day before planned surgery, and uptake will be determined using microscopy in the excised tissue |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sanne van Lith, PhD | Contact | 0031243613813 | sanne.vanlith@radboudumc.nl | |
| Martin Gotthardt, MD, prof | Contact | Martin.Gotthardt@radboudumc.nl |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Radboud University Medical Center | Recruiting | Nijmegen | Gelderland | 6525 GA | Netherlands |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39405026 | Derived | Jansen TJP, Tokgoz S, Buitinga M, van Lith SAM, Joosten L, Frielink C, Smeets EMM, Stommel MWJ, van der Kolk MB, de Galan BE, Brom M, Boss M, Gotthardt M. Validation of radiolabelled exendin for beta cell imaging by ex vivo autoradiography and immunohistochemistry of human pancreas. EJNMMI Res. 2024 Oct 15;14(1):96. doi: 10.1186/s13550-024-01159-6. |
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| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
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| IRDye800CW-exendin-4 | Drug | Injection of IRDye800CW-exendin-4 and localization of the tracer in excised pancreatic tissue using fluorescence microscopy |
|
| Gene expression | Gene expression levels will be determined with quantitative polymerase chain reaction (qPCR) | Gene expression will be determined in the excised pancreatic tissue immediately after resection |