Your browser doesn't support javascript.
loading
Localized rest and stress human cardiac creatine kinase reaction kinetics at 3 T.
Clarke, William T; Peterzan, Mark A; Rayner, Jennifer J; Sayeed, Rana A; Petrou, Mario; Krasopoulos, George; Lake, Hannah A; Raman, Betty; Watson, William D; Cox, Pete; Hundertmark, Moritz J; Apps, Andrew P; Lygate, Craig A; Neubauer, Stefan; Rider, Oliver J; Rodgers, Christopher T.
Afiliação
  • Clarke WT; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Peterzan MA; Wellcome Centre for Integrative Neuroimaging, FMRIB, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Rayner JJ; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Sayeed RA; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Petrou M; Department of Cardiothoracic Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Krasopoulos G; Department of Cardiothoracic Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Lake HA; Department of Cardiothoracic Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Raman B; Department of Cardiovascular Medicine, University of Oxford, Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford, UK.
  • Watson WD; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Cox P; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Hundertmark MJ; Department of Physiology Anatomy, University of Oxford, Parks Road, Sherrington Building, Oxford, UK.
  • Apps AP; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Lygate CA; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Neubauer S; Department of Cardiovascular Medicine, University of Oxford, Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford, UK.
  • Rider OJ; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Rodgers CT; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine RDM, University of Oxford, John Radcliffe Hospital, Oxford, UK.
NMR Biomed ; 32(6): e4085, 2019 06.
Article em En | MEDLINE | ID: mdl-30920054
Changes in the kinetics of the creatine kinase (CK) shuttle are sensitive markers of cardiac energetics but are typically measured at rest and in the prone position. This study aims to measure CK kinetics during pharmacological stress at 3 T, with measurement in the supine position. A shorter "stressed saturation transfer" (StreST) extension to the triple repetition time saturation transfer (TRiST) method is proposed. We assess scanning in a supine position and validate the MR measurement against biopsy assay of CK activity. We report normal ranges of stress CK forward rate (kfCK ) for healthy volunteers and obese patients. TRiST measures kfCK in 40 min at 3 T. StreST extends the previously developed TRiST to also make a further kfCK measurement during <20 min of dobutamine stress. We test our TRiST implementation in skeletal muscle and myocardium in both prone and supine positions. We evaluate StreST in the myocardium of six healthy volunteers and 34 obese subjects. We validated MR-measured kfCK against biopsy assays of CK activity. TRiST kfCK values matched literature values in skeletal muscle (kfCK  = 0.25 ± 0.03 s-1 vs 0.27 ± 0.03 s-1 ) and myocardium when measured in the prone position (0.32 ± 0.15 s-1 ), but a significant difference was found for TRiST kfCK measured supine (0.24 ± 0.12 s-1 ). This difference was because of different respiratory- and cardiac-motion-induced B0 changes in the two positions. Using supine TRiST, cardiac kfCK values for normal-weight subjects were 0.15 ± 0.09 s-1 at rest and 0.17 ± 0.15 s-1 during stress. For obese subjects, kfCK was 0.16 ± 0.07 s-1 at rest and 0.17 ± 0.10 s-1 during stress. Rest myocardial kfCK and CK activity from LV biopsies of the same subjects correlated (R = 0.43, p = 0.03). We present an independent implementation of TRiST on the Siemens platform using a commercially available coil. Our extended StreST protocol enables cardiac kfCK to be measured during dobutamine-induced stress in the supine position.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Descanso / Estresse Fisiológico / Espectroscopia de Ressonância Magnética / Creatina Quinase / Coração Tipo de estudo: Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: NMR Biomed Assunto da revista: DIAGNOSTICO POR IMAGEM / MEDICINA NUCLEAR Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Descanso / Estresse Fisiológico / Espectroscopia de Ressonância Magnética / Creatina Quinase / Coração Tipo de estudo: Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: NMR Biomed Assunto da revista: DIAGNOSTICO POR IMAGEM / MEDICINA NUCLEAR Ano de publicação: 2019 Tipo de documento: Article