<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Joergensen SH</submitter><funding>NIBIB NIH HHS</funding><funding>Danmarks Frie Forskningsfond</funding><funding>Hjerteforeningen</funding><pagination>34</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9169396</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Hyperpolarized (HP) [1-&lt;sup>13&lt;/sup>C]pyruvate cardiovascular magnetic resonance (CMR) imaging can visualize the uptake and intracellular conversion of [1-&lt;sup>13&lt;/sup>C]pyruvate to either [1-&lt;sup>13&lt;/sup>C]lactate or &lt;sup>13&lt;/sup>C-bicarbonate depending on the prevailing metabolic state. The aim of the present study was to combine an adenosine stress test with HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR to detect cardiac metabolism in the healthy human heart at rest and during moderate stress.&lt;h4>Methods&lt;/h4>A prospective descriptive study was performed between October 2019 and August 2020. Healthy human subjects underwent cine CMR and HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR at rest and during adenosine stress. HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR images were acquired at the mid-left-ventricle (LV) level. Semi-quantitative assessment of first-pass myocardial [1-&lt;sup>13&lt;/sup>C]pyruvate perfusion and metabolism were assessed. Paired t-tests were used to compare mean values at rest and during stress.&lt;h4>Results&lt;/h4>Six healthy subjects (two female), age 29 ± 7 years were studied and no adverse reactions occurred. Myocardial [1-&lt;sup>13&lt;/sup>C]pyruvate perfusion was significantly increased during stress with a reduction in time-to-peak from 6.2 ± 2.8 to 2.7 ± 1.3 s, p = 0.02. This higher perfusion was accompanied by an overall increased myocardial uptake and metabolism. The conversion rate constant (k&lt;sub>PL&lt;/sub>) for lactate increased from 11 ± 9 *10&lt;sup>-3&lt;/sup> to 20 ± 10 * 10&lt;sup>-3&lt;/sup> s&lt;sup>-1&lt;/sup>, p = 0.04. The pyruvate oxidation rate (k&lt;sub>PB&lt;/sub>) increased from 4 ± 4 *10&lt;sup>-3&lt;/sup> to 12 ± 7 *10&lt;sup>-3&lt;/sup> s&lt;sup>-1&lt;/sup>, p = 0.008. This increase in carbohydrate metabolism was positively correlated with heart rate (R&lt;sup>2&lt;/sup> = 0.44, p = 0.02).&lt;h4>Conclusions&lt;/h4>Adenosine stress testing combined with HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR is feasible and well-tolerated in healthy subjects. We observed an increased pyruvate oxidation during cardiac stress. The present study is an important step in the translation of HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR into clinical cardiac imaging. Trial registration EUDRACT, 2018-003533-15. Registered 4th of December 2018, https://www.clinicaltrialsregister.eu/ctr-search/search?query=2018-003533-15.</pubmed_abstract><journal>Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance</journal><pubmed_title>Detection of increased pyruvate dehydrogenase flux in the human heart during adenosine stress test using hyperpolarized [1-&lt;sup>13&lt;/sup>C]pyruvate cardiovascular magnetic resonance imaging.</pubmed_title><pmcid>PMC9169396</pmcid><funding_grant_id>18-R124-A8429-22093</funding_grant_id><funding_grant_id>P41 EB015908</funding_grant_id><funding_grant_id>9039-00157B</funding_grant_id><pubmed_authors>Bogh N</pubmed_authors><pubmed_authors>Bertelsen LB</pubmed_authors><pubmed_authors>Schulte RF</pubmed_authors><pubmed_authors>Joergensen SH</pubmed_authors><pubmed_authors>Hansen ESS</pubmed_authors><pubmed_authors>Laustsen C</pubmed_authors><pubmed_authors>Malloy C</pubmed_authors><pubmed_authors>Wiggers H</pubmed_authors><pubmed_authors>Staehr PB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detection of increased pyruvate dehydrogenase flux in the human heart during adenosine stress test using hyperpolarized [1-&lt;sup>13&lt;/sup>C]pyruvate cardiovascular magnetic resonance imaging.</name><description>&lt;h4>Background&lt;/h4>Hyperpolarized (HP) [1-&lt;sup>13&lt;/sup>C]pyruvate cardiovascular magnetic resonance (CMR) imaging can visualize the uptake and intracellular conversion of [1-&lt;sup>13&lt;/sup>C]pyruvate to either [1-&lt;sup>13&lt;/sup>C]lactate or &lt;sup>13&lt;/sup>C-bicarbonate depending on the prevailing metabolic state. The aim of the present study was to combine an adenosine stress test with HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR to detect cardiac metabolism in the healthy human heart at rest and during moderate stress.&lt;h4>Methods&lt;/h4>A prospective descriptive study was performed between October 2019 and August 2020. Healthy human subjects underwent cine CMR and HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR at rest and during adenosine stress. HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR images were acquired at the mid-left-ventricle (LV) level. Semi-quantitative assessment of first-pass myocardial [1-&lt;sup>13&lt;/sup>C]pyruvate perfusion and metabolism were assessed. Paired t-tests were used to compare mean values at rest and during stress.&lt;h4>Results&lt;/h4>Six healthy subjects (two female), age 29 ± 7 years were studied and no adverse reactions occurred. Myocardial [1-&lt;sup>13&lt;/sup>C]pyruvate perfusion was significantly increased during stress with a reduction in time-to-peak from 6.2 ± 2.8 to 2.7 ± 1.3 s, p = 0.02. This higher perfusion was accompanied by an overall increased myocardial uptake and metabolism. The conversion rate constant (k&lt;sub>PL&lt;/sub>) for lactate increased from 11 ± 9 *10&lt;sup>-3&lt;/sup> to 20 ± 10 * 10&lt;sup>-3&lt;/sup> s&lt;sup>-1&lt;/sup>, p = 0.04. The pyruvate oxidation rate (k&lt;sub>PB&lt;/sub>) increased from 4 ± 4 *10&lt;sup>-3&lt;/sup> to 12 ± 7 *10&lt;sup>-3&lt;/sup> s&lt;sup>-1&lt;/sup>, p = 0.008. This increase in carbohydrate metabolism was positively correlated with heart rate (R&lt;sup>2&lt;/sup> = 0.44, p = 0.02).&lt;h4>Conclusions&lt;/h4>Adenosine stress testing combined with HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR is feasible and well-tolerated in healthy subjects. We observed an increased pyruvate oxidation during cardiac stress. The present study is an important step in the translation of HP [1-&lt;sup>13&lt;/sup>C]pyruvate CMR into clinical cardiac imaging. Trial registration EUDRACT, 2018-003533-15. Registered 4th of December 2018, https://www.clinicaltrialsregister.eu/ctr-search/search?query=2018-003533-15.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2024-11-15T15:46:48.923Z</modification><creation>2024-11-15T15:46:48.923Z</creation></dates><accession>S-EPMC9169396</accession><cross_references><pubmed>35658896</pubmed><doi>10.1186/s12968-022-00860-6</doi></cross_references></HashMap>