Steven K. White
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Steven K. White has a total of 52 co-authors. Here are the top co-authors by number of shared publications:
- James Charles Moon
MyCardium AI Imaging Core Lab, Institute of Cardiovascular Science, University College London and Barts Heart Centre, St Bartholomew's Hospital, London, UK
5 shared publications - Marianna Fontana
Division of Medicine, National Amyloidosis Centre, University College London, London, UK
3 shared publications - Stefan Kazimierz Piechnik
Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom
3 shared publications - Daniel M Sado
The Heart Hospital Imaging Centre, The Heart Hospital, London and University College, London, UK
2 shared publications - Derek John Hausenloy
National Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore
2 shared publications - Heerajnarain Bulluck
Yorkshire Heart Centre, Leeds General Infirmary, Leeds Teaching Hospitals NHS Trust, Leeds LS1 3EX, UK
2 shared publications
Latest Publications
- 1 March 2016
- Published by Wolters Kluwer Health in Circulation: Cardiovascular Imaging
- Vol. 9 (3) , e003900
Quantifying the Area at Risk in Reperfused ST-Segment–Elevation Myocardial Infarction Patients Using Hybrid Cardiac Positron Emission Tomography–Magnetic Resonance Imaging
Background—: Hybrid positron emission tomography and magnetic resonance allows the advantages of magnetic resonance in tissue characterizing the myocardium to be combined with the unique metabolic insights of positron emission tomography. We hypothesized that the area of reduced myocardial glucose uptake would closely match the area at risk delineated by T2 mapping in ST-segment–elevation myocardial infarction patients. Methods and Results—: Hybrid positron emission tomography and magnetic resonance using 18 F-fluorodeoxyglucose (FDG) for glucose uptake was performed in 21 ST-segment–elevation myocardial infarction patients at a median of 5 days. Follow-up scans were performed in a subset of patients 12 months later. The area of reduced FDG uptake was significantly larger than the infarct size quantified by late gadolinium enhancement (37.2±11.6% versus 22.3±11.7%; P P =0.10, R=0.98, bias 0.9±4.4%). On the follow-up scans, the area of reduced FDG uptake was significantly smaller in size when compared with the acute scans (19.5 [6.3%–31.8%] versus 44.0 [21.3%–55.3%]; P =0.002) and closely correlated with the areas of late gadolinium enhancement (R 0.98) with a small bias of 2.0±5.6%. An FDG uptake of ≥45% on the acute scans could predict viable myocardium on the follow-up scan. Both transmural extent of late gadolinium enhancement and FDG uptake on the acute scan performed equally well to predict segmental wall motion recovery. Conclusions—: Hybrid positron emission tomography and magnetic resonance in the reperfused ST-segment–elevation myocardial infarction patients showed reduced myocardial glucose uptake within the area at risk and closely matched the area at risk delineated by T2 mapping. FDG uptake, as well as transmural extent of late gadolinium enhancement, acutely can identify viable myocardial segments.
- 1 March 2016
- Published by Wolters Kluwer Health in Circulation: Cardiovascular Imaging
- Vol. 9 (3) , e003900
Quantifying the Area at Risk in Reperfused ST-Segment–Elevation Myocardial Infarction Patients Using Hybrid Cardiac Positron Emission Tomography–Magnetic Resonance Imaging
Background—: Hybrid positron emission tomography and magnetic resonance allows the advantages of magnetic resonance in tissue characterizing the myocardium to be combined with the unique metabolic insights of positron emission tomography. We hypothesized that the area of reduced myocardial glucose uptake would closely match the area at risk delineated by T2 mapping in ST-segment–elevation myocardial infarction patients. Methods and Results—: Hybrid positron emission tomography and magnetic resonance using 18 F-fluorodeoxyglucose (FDG) for glucose uptake was performed in 21 ST-segment–elevation myocardial infarction patients at a median of 5 days. Follow-up scans were performed in a subset of patients 12 months later. The area of reduced FDG uptake was significantly larger than the infarct size quantified by late gadolinium enhancement (37.2±11.6% versus 22.3±11.7%; P P =0.10, R=0.98, bias 0.9±4.4%). On the follow-up scans, the area of reduced FDG uptake was significantly smaller in size when compared with the acute scans (19.5 [6.3%–31.8%] versus 44.0 [21.3%–55.3%]; P =0.002) and closely correlated with the areas of late gadolinium enhancement (R 0.98) with a small bias of 2.0±5.6%. An FDG uptake of ≥45% on the acute scans could predict viable myocardium on the follow-up scan. Both transmural extent of late gadolinium enhancement and FDG uptake on the acute scan performed equally well to predict segmental wall motion recovery. Conclusions—: Hybrid positron emission tomography and magnetic resonance in the reperfused ST-segment–elevation myocardial infarction patients showed reduced myocardial glucose uptake within the area at risk and closely matched the area at risk delineated by T2 mapping. FDG uptake, as well as transmural extent of late gadolinium enhancement, acutely can identify viable myocardial segments.
- Open Access
- 1 January 2015
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 17 (1) , 1-10
T1 mapping and T2 mapping at 3T for quantifying the area-at-risk in reperfused STEMI patients
- 1 January 2015
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 17 (1) , 1-10
Open AccessT1 mapping and T2 mapping at 3T for quantifying the area-at-risk in reperfused STEMI patients
- Open Access
- 5 December 2014
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 16 (1) , 1-9
Reproducibility of native myocardial T1 mapping in the assessment of Fabry disease and its role in early detection of cardiac involvement by cardiovascular magnetic resonance
- 5 December 2014
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 16 (1) , 1-9
Open AccessReproducibility of native myocardial T1 mapping in the assessment of Fabry disease and its role in early detection of cardiac involvement by cardiovascular magnetic resonance
- Open Access
- 1 January 2013
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 15 (1) , 1-11
Normal variation of magnetic resonance T1 relaxation times in the human population at 1.5 T using ShMOLLI
- 1 January 2013
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 15 (1) , 1-11
Open AccessNormal variation of magnetic resonance T1 relaxation times in the human population at 1.5 T using ShMOLLI
- Open Access
- 1 January 2012
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 14 (1) , 87-6
Comparison of T1 mapping techniques for ECV quantification. Histological validation and reproducibility of ShMOLLI versus multibreath-hold T1 quantification equilibrium contrast CMR
- 1 January 2012
- Published by Elsevier in Journal of Cardiovascular Magnetic Resonance
- Vol. 14 (1) , 87-6
Open AccessComparison of T1 mapping techniques for ECV quantification. Histological validation and reproducibility of ShMOLLI versus multibreath-hold T1 quantification equilibrium contrast CMR