Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction

<p><strong>Background:</strong>&nbsp;Why some but not all patients with severe AS (SevAS) develop otherwise unexplained reduced systolic function is unclear. We investigate the hypothesis that reduced creatine kinase (CK) capacity and/or flux is associated with this transition....

Full description

Bibliographic Details
Main Authors: Peterzan, MA, Clarke, WT, Lygate, CA, Lake, HA, Lau, JYC, Miller, JJ, Johnson, E, Rayner, JJ, Hundertmark, MJ, Sayeed, R, Petrou, M, Krasopoulos, G, Srivastava, V, Neubauer, S, Rodgers, C, Rider, OJ
Format: Journal article
Language:English
Published: Lippincott, Williams & Wilkins 2020
_version_ 1797060329939664896
author Peterzan, MA
Clarke, WT
Lygate, CA
Lake, HA
Lau, JYC
Miller, JJ
Johnson, E
Rayner, JJ
Hundertmark, MJ
Sayeed, R
Petrou, M
Krasopoulos, G
Srivastava, V
Neubauer, S
Rodgers, C
Rider, OJ
author_facet Peterzan, MA
Clarke, WT
Lygate, CA
Lake, HA
Lau, JYC
Miller, JJ
Johnson, E
Rayner, JJ
Hundertmark, MJ
Sayeed, R
Petrou, M
Krasopoulos, G
Srivastava, V
Neubauer, S
Rodgers, C
Rider, OJ
author_sort Peterzan, MA
collection OXFORD
description <p><strong>Background:</strong>&nbsp;Why some but not all patients with severe AS (SevAS) develop otherwise unexplained reduced systolic function is unclear. We investigate the hypothesis that reduced creatine kinase (CK) capacity and/or flux is associated with this transition.</p> <p><strong>Methods:</strong>&nbsp;102 participants were recruited to five groups: moderate AS (ModAS, n=13), severe AS, LVEF &ge;55% (SevAS-pEF, n=37), severe AS, LVEF&lt;55% (SevAS-rEF, n=15), healthy volunteers with non-hypertrophied hearts with normal systolic function (NHv, n=30), and patients with non-hypertrophied, non-pressure loaded hearts with normal systolic function undergoing cardiac surgery and donating LV biopsy (NHbx, n=7). All underwent CMR imaging and&nbsp;<sup>31</sup>P magnetic resonance spectroscopy (MRS) for myocardial energetics. LV biopsies (AS and NHBx) were analysed for; CK total activity, CK isoforms, citrate synthase (CS) activity and total creatine. Using serial block-face scanning electron microscopy, mitochondria-sarcomere diffusion distances were calculated.</p> <p><strong>Results:</strong>&nbsp;In the absence of failure, CK flux was lower in the presence of AS (by 32%, p=0.04), driven primarily by reduction in PCr/ATP (by 17%, p &lt;0.001), with CK k<sub>f</sub>&nbsp;unchanged (p=0.46),and is present in ModAS. Although lowest in the SevAS-rEF group, CK flux was not different to the SevAS-pEF group (p&gt;0.99). Accompanying the fall in CK flux, total CK and CS activities, and absolute activities of MtCK and CK-MM were also lower (p&lt;0.02, all analyses). Median mitochondria-sarcomere diffusion distances correlated well with CK total activity (r=0.86, p=.003).</p> <p><strong>Conclusions:</strong>&nbsp;Total CK capacity is reduced in SevAS, with median values lowest in those with systolic failure, consistent with reduced energy supply reserve. Despite this, in vivo MRS measures of resting CK flux suggest that ATP delivery is reduced earlier, at the moderate AS stage, but where LV function remains preserved.&nbsp;These&nbsp;findings show that significant energetic impairment is already established in moderate AS, and suggest a fall in CK flux is not per se the cause of transition to systolic failure. However, as ATP demands increase with AS severity this could increase susceptibility to systolic failure. As such, targeting CK capacity and/or flux may be a therapeutic strategy to prevent/treat systolic failure in AS.</p>
first_indexed 2024-03-06T20:15:37Z
format Journal article
id oxford-uuid:2c0ec7e3-0681-4ff4-b5b3-232ec3b0c784
institution University of Oxford
language English
last_indexed 2024-03-06T20:15:37Z
publishDate 2020
publisher Lippincott, Williams & Wilkins
record_format dspace
spelling oxford-uuid:2c0ec7e3-0681-4ff4-b5b3-232ec3b0c7842022-03-26T12:34:43ZCardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fractionJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2c0ec7e3-0681-4ff4-b5b3-232ec3b0c784EnglishSymplectic Elements Lippincott, Williams & Wilkins2020Peterzan, MAClarke, WTLygate, CALake, HALau, JYCMiller, JJJohnson, ERayner, JJHundertmark, MJSayeed, RPetrou, MKrasopoulos, GSrivastava, VNeubauer, SRodgers, CRider, OJ<p><strong>Background:</strong>&nbsp;Why some but not all patients with severe AS (SevAS) develop otherwise unexplained reduced systolic function is unclear. We investigate the hypothesis that reduced creatine kinase (CK) capacity and/or flux is associated with this transition.</p> <p><strong>Methods:</strong>&nbsp;102 participants were recruited to five groups: moderate AS (ModAS, n=13), severe AS, LVEF &ge;55% (SevAS-pEF, n=37), severe AS, LVEF&lt;55% (SevAS-rEF, n=15), healthy volunteers with non-hypertrophied hearts with normal systolic function (NHv, n=30), and patients with non-hypertrophied, non-pressure loaded hearts with normal systolic function undergoing cardiac surgery and donating LV biopsy (NHbx, n=7). All underwent CMR imaging and&nbsp;<sup>31</sup>P magnetic resonance spectroscopy (MRS) for myocardial energetics. LV biopsies (AS and NHBx) were analysed for; CK total activity, CK isoforms, citrate synthase (CS) activity and total creatine. Using serial block-face scanning electron microscopy, mitochondria-sarcomere diffusion distances were calculated.</p> <p><strong>Results:</strong>&nbsp;In the absence of failure, CK flux was lower in the presence of AS (by 32%, p=0.04), driven primarily by reduction in PCr/ATP (by 17%, p &lt;0.001), with CK k<sub>f</sub>&nbsp;unchanged (p=0.46),and is present in ModAS. Although lowest in the SevAS-rEF group, CK flux was not different to the SevAS-pEF group (p&gt;0.99). Accompanying the fall in CK flux, total CK and CS activities, and absolute activities of MtCK and CK-MM were also lower (p&lt;0.02, all analyses). Median mitochondria-sarcomere diffusion distances correlated well with CK total activity (r=0.86, p=.003).</p> <p><strong>Conclusions:</strong>&nbsp;Total CK capacity is reduced in SevAS, with median values lowest in those with systolic failure, consistent with reduced energy supply reserve. Despite this, in vivo MRS measures of resting CK flux suggest that ATP delivery is reduced earlier, at the moderate AS stage, but where LV function remains preserved.&nbsp;These&nbsp;findings show that significant energetic impairment is already established in moderate AS, and suggest a fall in CK flux is not per se the cause of transition to systolic failure. However, as ATP demands increase with AS severity this could increase susceptibility to systolic failure. As such, targeting CK capacity and/or flux may be a therapeutic strategy to prevent/treat systolic failure in AS.</p>
spellingShingle Peterzan, MA
Clarke, WT
Lygate, CA
Lake, HA
Lau, JYC
Miller, JJ
Johnson, E
Rayner, JJ
Hundertmark, MJ
Sayeed, R
Petrou, M
Krasopoulos, G
Srivastava, V
Neubauer, S
Rodgers, C
Rider, OJ
Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
title Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
title_full Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
title_fullStr Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
title_full_unstemmed Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
title_short Cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
title_sort cardiac energetics in patients with aortic stenosis and preserved versus reduced ejection fraction
work_keys_str_mv AT peterzanma cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT clarkewt cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT lygateca cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT lakeha cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT laujyc cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT millerjj cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT johnsone cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT raynerjj cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT hundertmarkmj cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT sayeedr cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT petroum cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT krasopoulosg cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT srivastavav cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT neubauers cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT rodgersc cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction
AT rideroj cardiacenergeticsinpatientswithaorticstenosisandpreservedversusreducedejectionfraction