Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging

Although non-invasive perfusion and viability imaging often provide the gateway to coronary revascularisation, current non-invasive imaging methods only report the surrogate markers of inducible hypoperfusion and presence or absence of myocardial scar, rather than actually visualising areas of ischa...

Full description

Bibliographic Details
Main Authors: Apps, A, Lau, J, Peterzan, M, Neubauer, S, Tyler, D, Rider, O
Format: Journal article
Language:English
Published: BMJ Publishing Group 2018
_version_ 1797100192893239296
author Apps, A
Lau, J
Peterzan, M
Neubauer, S
Tyler, D
Rider, O
author_facet Apps, A
Lau, J
Peterzan, M
Neubauer, S
Tyler, D
Rider, O
author_sort Apps, A
collection OXFORD
description Although non-invasive perfusion and viability imaging often provide the gateway to coronary revascularisation, current non-invasive imaging methods only report the surrogate markers of inducible hypoperfusion and presence or absence of myocardial scar, rather than actually visualising areas of ischaemia and/or viable myocardium. This may lead to suboptimal revascularisation decisions. Normally respiring (viable) cardiomyocytes convert pyruvate to acetyl-CoA and CO2/bicarbonate (via pyruvate dehydrogenase), but under ischaemic conditions characteristically shift this conversion to lactate (by lactate dehydrogenase). Imaging pyruvate metabolism thus has the potential to improve upon current imaging techniques. Using the novel hyperpolarisation technique of dynamic nuclear polarisation (DNP), the magnetic resonance signal of injected [1-13C]pyruvate can be transiently magnified >10 000 times over that seen in conventional MR spectroscopy, allowing the characteristic metabolic signatures of ischaemia (lactate production) and viability (CO2/bicarbonate production) to be directly imaged. As such DNP imaging of the downstream metabolism of [1-13C]pyruvate could surpass the diagnostic capabilities of contemporary ischaemia and viability testing. Here we review the technique, and with brief reference to the salient biochemistry, discuss its potential applications within cardiology. These include ischaemia and viability testing, and further characterisation of the altered metabolism seen at different stages during the natural history of heart failure.
first_indexed 2024-03-07T05:34:16Z
format Journal article
id oxford-uuid:e3594a56-a972-4144-b6bd-97d4d5d61fc9
institution University of Oxford
language English
last_indexed 2024-03-07T05:34:16Z
publishDate 2018
publisher BMJ Publishing Group
record_format dspace
spelling oxford-uuid:e3594a56-a972-4144-b6bd-97d4d5d61fc92022-03-27T10:08:25ZHyperpolarised magnetic resonance for in vivo real-time metabolic imagingJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e3594a56-a972-4144-b6bd-97d4d5d61fc9EnglishSymplectic Elements at OxfordBMJ Publishing Group2018Apps, ALau, JPeterzan, MNeubauer, STyler, DRider, OAlthough non-invasive perfusion and viability imaging often provide the gateway to coronary revascularisation, current non-invasive imaging methods only report the surrogate markers of inducible hypoperfusion and presence or absence of myocardial scar, rather than actually visualising areas of ischaemia and/or viable myocardium. This may lead to suboptimal revascularisation decisions. Normally respiring (viable) cardiomyocytes convert pyruvate to acetyl-CoA and CO2/bicarbonate (via pyruvate dehydrogenase), but under ischaemic conditions characteristically shift this conversion to lactate (by lactate dehydrogenase). Imaging pyruvate metabolism thus has the potential to improve upon current imaging techniques. Using the novel hyperpolarisation technique of dynamic nuclear polarisation (DNP), the magnetic resonance signal of injected [1-13C]pyruvate can be transiently magnified >10 000 times over that seen in conventional MR spectroscopy, allowing the characteristic metabolic signatures of ischaemia (lactate production) and viability (CO2/bicarbonate production) to be directly imaged. As such DNP imaging of the downstream metabolism of [1-13C]pyruvate could surpass the diagnostic capabilities of contemporary ischaemia and viability testing. Here we review the technique, and with brief reference to the salient biochemistry, discuss its potential applications within cardiology. These include ischaemia and viability testing, and further characterisation of the altered metabolism seen at different stages during the natural history of heart failure.
spellingShingle Apps, A
Lau, J
Peterzan, M
Neubauer, S
Tyler, D
Rider, O
Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging
title Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging
title_full Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging
title_fullStr Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging
title_full_unstemmed Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging
title_short Hyperpolarised magnetic resonance for in vivo real-time metabolic imaging
title_sort hyperpolarised magnetic resonance for in vivo real time metabolic imaging
work_keys_str_mv AT appsa hyperpolarisedmagneticresonanceforinvivorealtimemetabolicimaging
AT lauj hyperpolarisedmagneticresonanceforinvivorealtimemetabolicimaging
AT peterzanm hyperpolarisedmagneticresonanceforinvivorealtimemetabolicimaging
AT neubauers hyperpolarisedmagneticresonanceforinvivorealtimemetabolicimaging
AT tylerd hyperpolarisedmagneticresonanceforinvivorealtimemetabolicimaging
AT ridero hyperpolarisedmagneticresonanceforinvivorealtimemetabolicimaging