Show simple item record

dc.contributor.authorPieles, GE
dc.contributor.authorDorobantu, D-M
dc.contributor.authorCaterini, JE
dc.contributor.authorCifra, B
dc.contributor.authorReyes, J
dc.contributor.authorRoldan Ramos, S
dc.contributor.authorHannon, E
dc.contributor.authorWilliams, CA
dc.contributor.authorHumpl, T
dc.contributor.authorMertens, L
dc.contributor.authorWells, GD
dc.contributor.authorFriedberg, MK
dc.date.accessioned2024-09-26T11:14:30Z
dc.date.issued2024-09-11
dc.date.updated2024-09-26T10:38:19Z
dc.description.abstractDespite exercise intolerance being predictive of outcomes in pulmonary arterial hypertension (PAH), its underlying cardiac mechanisms are not well described. The aim of the study was to explore the biventricular response to exercise and its associations with cardiorespiratory fitness in children with PAH. Participants underwent incremental cardiopulmonary exercise testing and simultaneous exercise echocardiography on a recumbent cycle ergometer. Linear mixed models were used to assess cardiac function variance and associations between cardiac and metabolic parameters during exercise. Eleven participants were included with a mean age of 13.4 ± 2.9 yr old. Right ventricle (RV) systolic pressure (RVsp) increased from a mean of 59 ± 25 mmHg at rest to 130 ± 40 mmHg at peak exercise (P < 0.001), whereas RV fractional area change (RV-FAC) and RV-free wall longitudinal strain (RVFW-Sl) worsened (35.2 vs. 27%, P = 0.09 and -16.6 vs. -14.6%, P = 0.1, respectively). At low- and moderate-intensity exercise, RVsp was positively associated with stroke volume and O2 pulse (P < 0.1). At high-intensity exercise, RV-FAC, RVFW-Sl, and left ventricular longitudinal strain were positively associated with oxygen uptake and O2 pulse (P < 0.1), whereas stroke volume decreased toward peak (P = 0.04). In children with PAH, the increase of pulmonary pressure alone does not limit peak exercise, but rather the concomitant reduced RV functional reserve, resulting in RV to pulmonary artery (RV-PA) uncoupling, worsening of interventricular interaction and LV dysfunction. A better mechanistic understanding of PAH exercise physiopathology can inform stress testing and cardiac rehabilitation in this population. New and Noteworthy - In children with pulmonary arterial hypertension, there is a marked increase in pulmonary artery pressure during physical activity, but this is not the underlying mechanism that limits exercise. Instead, right ventricle-to-pulmonary artery uncoupling occurs at the transition from moderate to high-intensity exercise and correlates with lower peak oxygen uptake. This highlights the more complex underlying pathological responses and the need for multiparametric assessment of cardiac function reserve in these patients when feasible.en_GB
dc.description.sponsorshipLabatt Family Heart Centeren_GB
dc.description.sponsorshipUK Research and Innovation (UKRI)en_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.format.extentH749-H764
dc.format.mediumPrint-Electronic
dc.identifier.citationVol. 327 (4), pp. H749-H764en_GB
dc.identifier.doihttps://doi.org/10.1152/ajpheart.00096.2024
dc.identifier.grantnumberMR/N0137941/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/137546
dc.identifierORCID: 0000-0001-6840-072X (Hannon, Eilis)
dc.identifierResearcherID: T-1349-2019 (Hannon, Eilis)
dc.identifierORCID: 0000-0002-1740-6248 (Williams, Craig A)
dc.identifierScopusID: 57201609242 (Williams, Craig A)
dc.identifierResearcherID: AAQ-8954-2020 (Williams, Craig A)
dc.language.isoenen_GB
dc.publisherAmerican Physiological Societyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/39058433en_GB
dc.rights© 2024 The Authors. Licensed under Creative Commons Attribution CC-BY 4.0. Published by the American Physiological Society.en_GB
dc.subjectExercise testingen_GB
dc.subjectPulmonary hypertensionen_GB
dc.subjectRight ventricular functionen_GB
dc.subjectTissue-Doppler imagingen_GB
dc.subjectVentricular strainen_GB
dc.titleBiventricular responses to exercise and their relation to cardiorespiratory fitness in pediatric pulmonary hypertension.en_GB
dc.typeArticleen_GB
dc.date.available2024-09-26T11:14:30Z
dc.identifier.issn0363-6135
exeter.place-of-publicationUnited States
dc.descriptionThis is the final version. Available from American Physiological Society via the DOI in this record. en_GB
dc.descriptionData availability. Deidentified data used in this analysis cannot be made publicly available as it might contain sensitive information but can be shared upon reasonable request to the corresponding author, and data sharing agreements compliant with local and international data privacy laws are implemented.en_GB
dc.identifier.eissn1522-1539
dc.identifier.journalAmerican Journal of Physiology - Heart and Circulatory Physiologyen_GB
dc.relation.ispartofAm J Physiol Heart Circ Physiol, 327(4)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2024-07-12
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2024-09-11
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2024-09-26T11:04:58Z
refterms.versionFCDVoR
refterms.dateFOA2024-09-26T11:14:36Z
refterms.panelAen_GB
refterms.dateFirstOnline2024-09-11
exeter.rights-retention-statementNo


Files in this item

This item appears in the following Collection(s)

Show simple item record

© 2024 The Authors. Licensed under Creative Commons Attribution CC-BY 4.0. Published by the American Physiological Society.
Except where otherwise noted, this item's licence is described as © 2024 The Authors. Licensed under Creative Commons Attribution CC-BY 4.0. Published by the American Physiological Society.