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Detection of Atherosclerotic Inflammation by 68Ga-DOTATATE PET Compared to [18F]FDG PET Imaging.
Tarkin, Jason M; Joshi, Francis R; Evans, Nicholas R; Chowdhury, Mohammed M; Figg, Nichola L; Shah, Aarti V; Starks, Lakshi T; Martin-Garrido, Abel; Manavaki, Roido; Yu, Emma; Kuc, Rhoda E; Grassi, Luigi; Kreuzhuber, Roman; Kostadima, Myrto A; Frontini, Mattia; Kirkpatrick, Peter J; Coughlin, Patrick A; Gopalan, Deepa; Fryer, Tim D; Buscombe, John R; Groves, Ashley M; Ouwehand, Willem H; Bennett, Martin R; Warburton, Elizabeth A; Davenport, Anthony P; Rudd, James H F.
Afiliación
  • Tarkin JM; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Joshi FR; Heart Center, Rigshospitalet, Copenhagen, Denmark.
  • Evans NR; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
  • Chowdhury MM; Department of Vascular and Endovascular Surgery, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • Figg NL; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Shah AV; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Starks LT; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Martin-Garrido A; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Manavaki R; Department of Radiology, University of Cambridge, Cambridge, United Kingdom.
  • Yu E; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Kuc RE; Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge, United Kingdom.
  • Grassi L; Department of Hematology, University of Cambridge, and National Health Service Blood and Transport, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • Kreuzhuber R; Department of Hematology, University of Cambridge, and National Health Service Blood and Transport, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • Kostadima MA; Department of Hematology, University of Cambridge, and National Health Service Blood and Transport, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • Frontini M; Department of Hematology, University of Cambridge, and National Health Service Blood and Transport, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • Kirkpatrick PJ; Division of Neurosurgery, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • Coughlin PA; Department of Vascular and Endovascular Surgery, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • Gopalan D; Department of Radiology, University of Cambridge, Cambridge, United Kingdom; Department of Radiology, Hammersmith Hospital, London, United Kingdom.
  • Fryer TD; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
  • Buscombe JR; Department of Nuclear Medicine, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • Groves AM; Institute of Nuclear Medicine, University College London, London, United Kingdom.
  • Ouwehand WH; Department of Hematology, University of Cambridge, and National Health Service Blood and Transport, Cambridge Biomedical Campus, Cambridge, United Kingdom; Department of Human Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, United Kingdom.
  • Bennett MR; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Warburton EA; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
  • Davenport AP; Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge, United Kingdom.
  • Rudd JH; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, United Kingdom. Electronic address: jhfr2@cam.ac.uk.
J Am Coll Cardiol ; 69(14): 1774-1791, 2017 Apr 11.
Article en En | MEDLINE | ID: mdl-28385306
ABSTRACT

BACKGROUND:

Inflammation drives atherosclerotic plaque rupture. Although inflammation can be measured using fluorine-18-labeled fluorodeoxyglucose positron emission tomography ([18F]FDG PET), [18F]FDG lacks cell specificity, and coronary imaging is unreliable because of myocardial spillover.

OBJECTIVES:

This study tested the efficacy of gallium-68-labeled DOTATATE (68Ga-DOTATATE), a somatostatin receptor subtype-2 (SST2)-binding PET tracer, for imaging atherosclerotic inflammation.

METHODS:

We confirmed 68Ga-DOTATATE binding in macrophages and excised carotid plaques. 68Ga-DOTATATE PET imaging was compared to [18F]FDG PET imaging in 42 patients with atherosclerosis.

RESULTS:

Target SSTR2 gene expression occurred exclusively in "proinflammatory" M1 macrophages, specific 68Ga-DOTATATE ligand binding to SST2 receptors occurred in CD68-positive macrophage-rich carotid plaque regions, and carotid SSTR2 mRNA was highly correlated with in vivo 68Ga-DOTATATE PET signals (r = 0.89; 95% confidence interval [CI] 0.28 to 0.99; p = 0.02). 68Ga-DOTATATE mean of maximum tissue-to-blood ratios (mTBRmax) correctly identified culprit versus nonculprit arteries in patients with acute coronary syndrome (median difference 0.69; interquartile range [IQR] 0.22 to 1.15; p = 0.008) and transient ischemic attack/stroke (median difference 0.13; IQR 0.07 to 0.32; p = 0.003). 68Ga-DOTATATE mTBRmax predicted high-risk coronary computed tomography features (receiver operating characteristics area under the curve [ROC AUC] 0.86; 95% CI 0.80 to 0.92; p < 0.0001), and correlated with Framingham risk score (r = 0.53; 95% CI 0.32 to 0.69; p <0.0001) and [18F]FDG uptake (r = 0.73; 95% CI 0.64 to 0.81; p < 0.0001). [18F]FDG mTBRmax differentiated culprit from nonculprit carotid lesions (median difference 0.12; IQR 0.0 to 0.23; p = 0.008) and high-risk from lower-risk coronary arteries (ROC AUC 0.76; 95% CI 0.62 to 0.91; p = 0.002); however, myocardial [18F]FDG spillover rendered coronary [18F]FDG scans uninterpretable in 27 patients (64%). Coronary 68Ga-DOTATATE PET scans were readable in all patients.

CONCLUSIONS:

We validated 68Ga-DOTATATE PET as a novel marker of atherosclerotic inflammation and confirmed that 68Ga-DOTATATE offers superior coronary imaging, excellent macrophage specificity, and better power to discriminate high-risk versus low-risk coronary lesions than [18F]FDG. (Vascular Inflammation Imaging Using Somatostatin Receptor Positron Emission Tomography [VISION]; NCT02021188).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Compuestos Organometálicos / Fluorodesoxiglucosa F18 / Aterosclerosis / Tomografía Computarizada por Tomografía de Emisión de Positrones / Inflamación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Compuestos Organometálicos / Fluorodesoxiglucosa F18 / Aterosclerosis / Tomografía Computarizada por Tomografía de Emisión de Positrones / Inflamación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido