Cross-sectional and Test-Retest Characterization of PET with [18F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes

Autor: Rudolph L. Leibel, Paul L. Harris, Robin Goland, Matthew J. Freeby, Antonella Maffei, Masanori Ichise, Patricia Kringas, Chaitan Divgi
Jazyk: angličtina
Předmět:
0301 basic medicine
Male
Cancer Research
Fluorine Radioisotopes
Test-Retest
PET
medicine.medical_treatment
Tetrabenazine
Bioinformatics
Insulin-Secreting Cells
Insulin
Medicine(all)
medicine.diagnostic_test
Diabetes
Middle Aged
3. Good health
medicine.anatomical_structure
Oncology
Positron emission tomography
Biomarker (medicine)
Female
Pancreas
Protein Binding
Research Article
Adult
medicine.medical_specialty
[18F]FP-(+)-DTBZ
Urology
Test-retest
03 medical and health sciences
VMAT2
Diabetes mellitus
medicine
Humans
Radiology
Nuclear Medicine and imaging

Beta cell mass
Cell Size
Demography
Type 1 diabetes
business.industry
Case-control study
Binding potential
medicine.disease
030104 developmental biology
Diabetes Mellitus
Type 1

Glucose
Diabetes Mellitus
Type 2

Case-Control Studies
Positron-Emission Tomography
Vesicular Monoamine Transport Proteins
business
Zdroj: Molecular imaging and biology (2015). doi:10.1007/s11307-015-0888-7
info:cnr-pdr/source/autori:Freeby MJ, Kringas P, Goland RS, Leibel RL, Maffei A, Divgi C, Ichise M, Harris PE./titolo:Cross-sectional and Test-Retest Characterization of PET with [18F]FP-(+)-DTBZ for ? Cell Mass Estimates in Diabetes./doi:10.1007%2Fs11307-015-0888-7/rivista:Molecular imaging and biology/anno:2015/pagina_da:/pagina_a:/intervallo_pagine:/volume
Molecular Imaging and Biology
ISSN: 1536-1632
DOI: 10.1007/s11307-015-0888-7
Popis: Purpose The vesicular monoamine transporter, type 2 (VMAT2) is expressed by insulin producing β cells and was evaluated as a biomarker of β cell mass (BCM) by positron emission tomography (PET) with [18F]fluoropropyl-dihydrotetrabenazine ([18F]FP-(+)-DTBZ). Procedures We evaluated the feasibility of longitudinal pancreatic PET VMAT2 quantification in the pancreas in two studies of healthy controls and patients with type 1 or 2 diabetes. VMAT2 binding potential (BPND) was estimated voxelwise using a reference tissue method in a cross-sectional study, followed by assessment of reproducibility using a test-retest paradigm. Metabolic function was evaluated by stimulated c-peptide measurements. Results Pancreatic BPND was significantly decreased in patients with type 1 diabetes relative to controls and the test-retest variability was 9.4 %. Conclusions Pancreatic VMAT2 content is significantly reduced in long-term diabetes patients relative to controls and repeat scans are sufficiently reproducible to suggest the feasibility clinically VMAT2 measurements in longitudinal studies of new onset diabetes. Electronic supplementary material The online version of this article (doi:10.1007/s11307-015-0888-7) contains supplementary material, which is available to authorized users.
Databáze: OpenAIRE