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Adjustment of vascular 2-deoxy-2-[18F]fluoro-D-glucose uptake values over time through a modeling approach.
Kafouris, Pavlos P; Koutagiar, Iosif P; Georgakopoulos, Alexandros T; Pianou, Nikoletta K; Metaxas, Marinos G; Spyrou, George M; Anagnostopoulos, Constantinos D.
Afiliação
  • Kafouris PP; Department of Informatics and Telecommunications, National and Kapodistrian University of Athens, Athens, Greece.
  • Koutagiar IP; Experimental Surgery, Clinical and Translational Research Centre, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
  • Georgakopoulos AT; First Department of Cardiology, Hippokration Hospital, Athens, Greece.
  • Pianou NK; Experimental Surgery, Clinical and Translational Research Centre, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
  • Metaxas MG; Experimental Surgery, Clinical and Translational Research Centre, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
  • Spyrou GM; Experimental Surgery, Clinical and Translational Research Centre, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
  • Anagnostopoulos CD; Bioinformatics ERA Chair, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Int J Cardiovasc Imaging ; 35(5): 955-964, 2019 May.
Article em En | MEDLINE | ID: mdl-30706352
To develop and test a model predicting 2-deoxy-2-[18F]fluoro-D-glucose ([18F]FDG) standardized uptake value (SUV) changes over time in the aorta and the superior vena cava (SVC). Maximum aortic SUV and mean SVC SUV were determined at two time points (T1 and T2) in the ascending (ASC), descending (DSC), abdominal (ABD) aorta, aortic arch (ARC) and SVC of patients who have undergone [18F]FDG PET/CT for clinical purposes. For SUV prediction at T2, linear and non-linear models of SUV difference for a given time change were developed in a derivation group. The results were tested in an independent validation group, whilst model reproducibility was tested in patients of the validation group who have undergone a second clinically indicated scan. Applying the linear model in the derivation group, there were no statistically significant differences in measurements obtained in the examined segments: mean differences ranged from 0 ± 0.10 in SVC to 0.01 ± 0.13 in ARC between measured and predicted SUV. In contrast, in the non-linear model, there were statistically significant differences in measurements, except in ARC, with mean differences ranging from 0.04 ± 0.14 in ARC to 0.28 ± 0.13 in ABD. In the validation group using the linear model, there were no statistically significant differences, with mean differences ranging from - 0.01 ± 0.08 in ASC to - 0.03 ± 0.11 in ABD. Regarding reproducibility, mean differences were no statistically significant, ranging from 0.004 ± 0.06 in ASC to - 0.02 ± 0.16 in ABD. We have developed a linear model allowing accurate and reproducible prediction of SUV changes over time in the aorta and SVC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aorta Abdominal / Aorta Torácica / Veia Cava Inferior / Compostos Radiofarmacêuticos / Fluordesoxiglucose F18 / Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Cardiovasc Imaging Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aorta Abdominal / Aorta Torácica / Veia Cava Inferior / Compostos Radiofarmacêuticos / Fluordesoxiglucose F18 / Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Cardiovasc Imaging Ano de publicação: 2019 Tipo de documento: Article