Test-retest repeatability of quantitative organ and tissue uptake using 20-minute dynamic multiparametric whole-body [18F]FDG PET/CT in patients with type 2 diabetes.
IF 3.1 3区 医学Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Jonathan M Baier, Kristian L Funck, Anna Dons-Jensen, Ole L Munk, Lars P Tolbod, Esben Laugesen, Per L Poulsen, Lars C Gormsen, André H Dias
{"title":"Test-retest repeatability of quantitative organ and tissue uptake using 20-minute dynamic multiparametric whole-body [<sup>18</sup>F]FDG PET/CT in patients with type 2 diabetes.","authors":"Jonathan M Baier, Kristian L Funck, Anna Dons-Jensen, Ole L Munk, Lars P Tolbod, Esben Laugesen, Per L Poulsen, Lars C Gormsen, André H Dias","doi":"10.1186/s13550-025-01249-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Recently developed dynamic whole-body PET/CT (D-WB PET/CT) protocols allow for measurements of potentially more precise metabolic parameters than the commonly used semiquantitative SUV. Most notable is the metabolic rate of FDG uptake (MR<sub>FDG</sub>), which reflects quantitative glucose uptake into tissues and organs. However, data on the reproducibility of MR<sub>FDG</sub> measurements are scarce, particularly in patients with perturbed glucose homeostasis such as type 2 diabetes. We therefore aimed to evaluate the test-retest repeatability of both MR<sub>FDG</sub> and SUV in these patients.</p><p><strong>Results: </strong>Fifteen participants (mean age 71 ± 7 years; 2 females) with type 2 diabetes underwent a short 20-minute [<sup>18</sup>F]FDG D-WB PET/CT after 6 h fasting on two consecutive days. Both SUV and MR<sub>FDG</sub> images were reconstructed from D-WB PET/CT data obtained 60-80 min post-injection of [<sup>18</sup>F]FDG. MR<sub>FDG</sub> and SUV data were measured in organs and tissues, and repeatability was assessed with Bland-Altman analysis, intraclass correlation coefficients (ICC), repeatability coefficients (RPC) and coefficients of variation (wCV). There was high repeatability of both SUV<sub>mean</sub> and MR<sub>FDG-mean</sub> in all measured organs (ICC range: 0.65-0.95 for SUV<sub>mean</sub> and 0.66-0.94 for MR<sub>FDG-mean</sub>). SUV<sub>mean</sub> generally demonstrated higher reliability (ICC) and lower variability (%RPC and %wCV) when compared to MR<sub>FDG-mean</sub>. However, MR<sub>FDG</sub> test-retest variation was < 19% in most analysed tissues, demonstrating that MR<sub>FDG</sub> may be used as a precise marker of treatment response.</p><p><strong>Conclusion: </strong>This study demonstrates that MR<sub>FDG</sub> calculated from D-WB PET/CT exhibit high repeatability, comparable to SUVs across most organs in patients with type 2 diabetes.</p>","PeriodicalId":11611,"journal":{"name":"EJNMMI Research","volume":"15 1","pages":"56"},"PeriodicalIF":3.1000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12069784/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EJNMMI Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13550-025-01249-z","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Recently developed dynamic whole-body PET/CT (D-WB PET/CT) protocols allow for measurements of potentially more precise metabolic parameters than the commonly used semiquantitative SUV. Most notable is the metabolic rate of FDG uptake (MRFDG), which reflects quantitative glucose uptake into tissues and organs. However, data on the reproducibility of MRFDG measurements are scarce, particularly in patients with perturbed glucose homeostasis such as type 2 diabetes. We therefore aimed to evaluate the test-retest repeatability of both MRFDG and SUV in these patients.
Results: Fifteen participants (mean age 71 ± 7 years; 2 females) with type 2 diabetes underwent a short 20-minute [18F]FDG D-WB PET/CT after 6 h fasting on two consecutive days. Both SUV and MRFDG images were reconstructed from D-WB PET/CT data obtained 60-80 min post-injection of [18F]FDG. MRFDG and SUV data were measured in organs and tissues, and repeatability was assessed with Bland-Altman analysis, intraclass correlation coefficients (ICC), repeatability coefficients (RPC) and coefficients of variation (wCV). There was high repeatability of both SUVmean and MRFDG-mean in all measured organs (ICC range: 0.65-0.95 for SUVmean and 0.66-0.94 for MRFDG-mean). SUVmean generally demonstrated higher reliability (ICC) and lower variability (%RPC and %wCV) when compared to MRFDG-mean. However, MRFDG test-retest variation was < 19% in most analysed tissues, demonstrating that MRFDG may be used as a precise marker of treatment response.
Conclusion: This study demonstrates that MRFDG calculated from D-WB PET/CT exhibit high repeatability, comparable to SUVs across most organs in patients with type 2 diabetes.
EJNMMI ResearchRADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍:
EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies.
The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.