Identifying active vascular microcalcification by 18F-sodium fluoride positron emission tomography

Agnese Irkle(University of Cambridge), Alex Vesey(University of Edinburgh), David Y. Lewis(University of Cambridge), Jeremy N. Skepper(University of Cambridge), Joseph Bird(University of Cambridge), Marc R. Dweck(University of Edinburgh), Francis R. Joshi(University of Cambridge), Ferdia A. Gallagher(University of Cambridge), Elizabeth A. Warburton(University of Cambridge), Martin R. Bennett(University of Cambridge), Kevin M. Brindle(University of Cambridge), David E. Newby(University of Edinburgh), James H.F. Rudd(University of Cambridge), Anthony P. Davenport(University of Cambridge)
Nature Communications
July 7, 2015
Cited by 454Open Access
Full Text

Abstract

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.


Related Papers

No related papers found

Powered by citation graph analysis