Glucose-stimulated Pancreatic Islet and Intestinal Blood Flow in Healthy Subjects and in Type 1 Diabetes (ISLET-PET)

Turku University Hospital (TYKS)

Status: Completed

Conditions: Type 1 Diabetes

Study type: Observational

Funder types: Other

Identifiers

NCT02547337

ISLET-PET

Details and patient eligibility

About

Type 1 diabetes is the major type of diabetes in the young. The pathophysiology still needs clarification in order to reach feasible means of preventing the disease. This study aims in defining the differences in pancreatic and intestinal blood flow between subjects with and without type 1 diabetes and validating the methodology to achieve this. Earlier animal studies have demonstrated changes in pancreatic islet blood flow using microspheres. The aim of this study is to test and validate a method for the assessment of islet perfusion in humans using molecular imaging. The investigators hypothesize that glucose-stimulated pancreatic perfusion is enhanced specifically in islets in healthy subjects and that this increase is mostly suppressed in subjects with type 1 diabetes.

Positron emission tomography (PET) is a non-invasive imaging technique, which can be used to study flow and metabolism of different organs. Using radiowater ([15O]H2O) and PET, cellular perfusion can be measured directly and noninvasively. Recently, diffusion weighted magnetic resonance imaging (DWI) has also been applied as a complimentary method for the assessment to quantitate changes in pancreatic blood flow.

In the study 10 healthy subjects and 10 subjects with type 1 diabetes will be imaged on two separate days. Pancreatic and intestinal perfusion are first measured with [15O]H2O and combined PET/magnetic resonance imaging before and 5 and 15 minutes after intravenous glucose infusion. On the second day, PET imaging is replaced by dynamic DWI conducted in the same time schedule and with intravenous glucose stimulation.

Enrollment: 11 patients

Sex: All

Ages: 18 to 30 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Criteria for healthy subjects

Inclusion criteria

• Healthy as judged by history and examination
• Age 18-30 years
• Body mass index (BMI) 18 - 27 kg/m2
• Normal 2 h oral glucose tolerance test

Exclusion criteria

• Any chronic disease
• Pregnancy
• Blood pressure > 140/90 mmHg
• Smoking
• Presence of any ferromagnetic objects in the body
• Any other condition that could possibly create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of the study results

Criteria for subjects with type 1 diabetes (T1D)

Inclusion criteria

• T1D diagnosed at least 5 years ago
• Age 18-30 years
• BMI 18 - 30 kg/m2
• Good or moderate glycemic control with long-acting insulin analogue combined with injections of rapid-acting insulin
• Uncomplicated T1D or with minor microvascular complications

Exclusion criteria

• Any other condition or disease possibly affecting circulation, as evaluated by a physician
• Pregnancy
• Blood pressure > 140/90 mmHg
• Smoking
• Presence of any ferromagnetic objects in the body
• Any other condition that could possibly create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of the study results

Trial design

11 participants in 2 patient groups

Type 1 diabetes

Healthy subjects