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Thresholds for Arterial Wall Inflammation Quantified by 18F-FDG PET Imaging: Implications for Vascular Interventional Studies.
van der Valk, Fleur M; Verweij, Simone L; Zwinderman, Koos A H; Strang, Aart C; Kaiser, Yannick; Marquering, Henk A; Nederveen, Aart J; Stroes, Erik S G; Verberne, Hein J; Rudd, James H F.
Afiliação
  • van der Valk FM; Department of Vascular Medicine, Academic Medical Centre, Amsterdam, the Netherlands. Electronic address: f.m.valkvander@amc.nl.
  • Verweij SL; Department of Vascular Medicine, Academic Medical Centre, Amsterdam, the Netherlands.
  • Zwinderman KA; Department of Clinical Epidemiology, Academic Medical Center, Amsterdam, the Netherlands.
  • Strang AC; Department of Vascular Medicine, Academic Medical Centre, Amsterdam, the Netherlands.
  • Kaiser Y; Department of Vascular Medicine, Academic Medical Centre, Amsterdam, the Netherlands.
  • Marquering HA; Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands; Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, the Netherlands; Department of Nuclear Medicine, Academic Medical Center, Amsterdam, the Netherlands.
  • Nederveen AJ; Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands.
  • Stroes ES; Department of Vascular Medicine, Academic Medical Centre, Amsterdam, the Netherlands.
  • Verberne HJ; Department of Nuclear Medicine, Academic Medical Center, Amsterdam, the Netherlands.
  • Rudd JH; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
JACC Cardiovasc Imaging ; 9(10): 1198-1207, 2016 10.
Article em En | MEDLINE | ID: mdl-27639759
ABSTRACT

OBJECTIVES:

This study assessed 5 frequently applied arterial 18fluorodeoxyglucose (18F-FDG) uptake metrics in healthy control subjects, those with risk factors and patients with cardiovascular disease (CVD), to derive uptake thresholds in each subject group. Additionally, we tested the reproducibility of these measures and produced recommended sample sizes for interventional drug studies.

BACKGROUND:

18F-FDG positron emission tomography (PET) can identify plaque inflammation as a surrogate endpoint for vascular interventional drug trials. However, an overview of 18F-FDG uptake metrics, threshold values, and reproducibility in healthy compared with diseased subjects is not available.

METHODS:

18F-FDG PET/CT of the carotid arteries and ascending aorta was performed in 83 subjects (61 ± 8 years) comprising 3 groups 25 healthy controls, 23 patients at increased CVD risk, and 35 patients with known CVD. We quantified 18F-FDG uptake across the whole artery, the most-diseased segment, and within all active segments over several pre-defined cutoffs. We report these data with and without background corrections. Finally, we determined measurement reproducibility and recommended sample sizes for future drug studies based on these results.

RESULTS:

All 18F-FDG uptake metrics were significantly different between healthy and diseased subjects for both the carotids and aorta. Thresholds of physiological 18F-FDG uptake were derived from healthy controls using the 90th percentile of their target to background ratio (TBR) value (TBRmax); whole artery TBRmax is 1.84 for the carotids and 2.68 in the aorta. These were exceeded by >52% of risk factor patients and >67% of CVD patients. Reproducibility was excellent in all study groups (intraclass correlation coefficient >0.95). Using carotid TBRmax as a primary endpoint resulted in sample size estimates approximately 20% lower than aorta.

CONCLUSIONS:

We report thresholds for physiological 18F-FDG uptake in the arterial wall in healthy subjects, which are exceeded by the majority of CVD patients. This remains true, independent of readout vessel, signal quantification method, or the use of background correction. We also confirm the high reproducibility of 18F-FDG PET measures of inflammation. Nevertheless, because of overlap between subject categories and the relatively small population studied, these data have limited generalizability until substantiated in larger, prospective event-driven studies. (Vascular Inflammation in Patients at Risk for Atherosclerotic Disease; NTR5006).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aorta / Aortite / Arterite / Artérias Carótidas / Doenças das Artérias Carótidas / Compostos Radiofarmacêuticos / Fluordesoxiglucose F18 / Tomografia por Emissão de Pósitrons / Placa Aterosclerótica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aorta / Aortite / Arterite / Artérias Carótidas / Doenças das Artérias Carótidas / Compostos Radiofarmacêuticos / Fluordesoxiglucose F18 / Tomografia por Emissão de Pósitrons / Placa Aterosclerótica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article