Vascular biomechanics and molecular disease activity in the thoracic aorta: a novel imaging method.

Savine C S Minderhoud, Alexander J Fletcher, Gillian MacNaught, Sebastien Cadet, Suze-Anne Korteland, Isabella Kardys, Dimitris Rizopoulos, Piotr Slomka, David E Newby, Jolien W Roos-Hesselink, Niki L Walker, Scott Semple, Alexander Hirsch, Marc R Dweck, Jolanda J Wentzel

Journal: European heart journal. Cardiovascular Imaging 2022;23(12):1698-1707

PMID: 35666823

Abstract

AIMS

The influence haemodynamics have on vessel wall pathobiology in aortic disease is incomplete. This aim of this study was to develop a repeatable method for assessing the relationship between aortic wall shear stress (WSS) and disease activity by fusing 4D flow cardiovascular magnetic resonance (CMR) with hybrid positron emission tomography (PET).

METHODS AND RESULTS

As part of an ongoing clinical trial, patients with bicuspid aortic valve (BAV) were prospectively imaged with both 18F-sodium fluoride (18F-NaF) PET, a marker of calcification activity, and 4D flow CMR. We developed novel software allowing accurate 3D co-registration and high-resolution comparison of aortic peak systolic WSS and 18F-NaF PET uptake (maximum tissue-to-background ratio). Intra-observer repeatability of both measurements was determined using Bland-Altman plots and intra-class correlation coefficients (ICCs). The relationship between localized WSS and 18F-NaF uptake was analysed using linear mixed-effect models. Twenty-three patients with BAV (median age 50 [44-55] years, 22% female) were included. Intra-observer repeatability for WSS (ICC = 0.92) and 18F-NaF (ICC = 0.91) measurements obtained within 1.4 ± 0.6 cm2 regions of interest was excellent. On multivariable analysis, 18F-NaF PET uptake was independently and negatively associated with WSS as well as diastolic blood pressure (both P < 0.05), adjusted for age.

CONCLUSION

Fused assessment of WSS and 18F-NaF PET uptake is feasible and repeatable, demonstrating a clear association between these two factors. This high spatial resolution approach has major potential to advance our understanding of the relationship between vascular haemodynamics and disease activity.

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

Address: Department of Cardiology, Erasmus Medical Center, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.; Department of Radiology and Nuclear Medicine, Erasmus Medical Center, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK.; Department of Child Health, University of Glasgow, School of Medicine and Dentistry, G51 4TF Glasgow, UK.; Edinburgh Imaging Facility, Queens Medical Research Institute, University of Edinburgh, EH16 4TJ Edinburgh, UK.; Department of Imaging (Division of Nuclear Cardiology), Cedars-Sinai Medical Centre, CA 90048 Los Angeles, CA, USA.; Department of Biostatistics, Erasmus Medical Center, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.; Scottish Adult Congenital Cardiac Service, Golden Jubilee National Hospital, G81 4DY Clydebank, UK.
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