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Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography.
Irkle, Agnese; Vesey, Alex T; Lewis, David Y; Skepper, Jeremy N; Bird, Joseph L E; Dweck, Marc R; Joshi, Francis R; Gallagher, Ferdia A; Warburton, Elizabeth A; Bennett, Martin R; Brindle, Kevin M; Newby, David E; Rudd, James H; Davenport, Anthony P.
Afiliação
  • Irkle A; Division of Experimental Medicine &Immunotherapeutics (EMIT), Department of Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Vesey AT; Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, EH16 4TJ, UK.
  • Lewis DY; Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, CB2 0RE, UK.
  • Skepper JN; Department of Physiology, Development and Neuroscience, Multi-Imaging Centre, University of Cambridge, Cambridge, CB2 3EG, UK.
  • Bird JL; Division of Experimental Medicine &Immunotherapeutics (EMIT), Department of Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Dweck MR; Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, EH16 4TJ, UK.
  • Joshi FR; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Gallagher FA; 1] Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, CB2 0RE, UK. [2] Department of Radiology, Box 218 Level 5, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Warburton EA; Department of Clinical Neurosciences, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Bennett MR; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Brindle KM; Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, CB2 0RE, UK.
  • Newby DE; Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, EH16 4TJ, UK.
  • Rudd JH; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Davenport AP; Division of Experimental Medicine &Immunotherapeutics (EMIT), Department of Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
Nat Commun ; 6: 7495, 2015 Jul 07.
Article em En | MEDLINE | ID: mdl-26151378
Vascular calcification is a complex biological process that is a hallmark of atherosclerosis. While macrocalcification confers plaque stability, microcalcification is a key feature of high-risk atheroma and is associated with increased morbidity and mortality. Positron emission tomography and X-ray computed tomography (PET/CT) imaging of atherosclerosis using (18)F-sodium fluoride ((18)F-NaF) has the potential to identify pathologically high-risk nascent microcalcification. However, the precise molecular mechanism of (18)F-NaF vascular uptake is still unknown. Here we use electron microscopy, autoradiography, histology and preclinical and clinical PET/CT to analyse (18)F-NaF binding. We show that (18)F-NaF adsorbs to calcified deposits within plaque with high affinity and is selective and specific. (18)F-NaF PET/CT imaging can distinguish between areas of macro- and microcalcification. This is the only currently available clinical imaging platform that can non-invasively detect microcalcification in active unstable atherosclerosis. The use of (18)F-NaF may foster new approaches to developing treatments for vascular calcification.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fluoreto de Sódio / Artérias Carótidas / Tomografia por Emissão de Pósitrons / Aterosclerose / Calcificação Vascular Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fluoreto de Sódio / Artérias Carótidas / Tomografia por Emissão de Pósitrons / Aterosclerose / Calcificação Vascular Idioma: En Ano de publicação: 2015 Tipo de documento: Article