Fitness and metabolic response to exercise in young adult survivors of childhood lymphoma.

Adolescent Blood cancer Global longitudinal strain Paediatrics Physical activity Survivors

Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
29 May 2023
Historique:
received: 16 11 2022
accepted: 13 05 2023
medline: 31 5 2023
pubmed: 29 5 2023
entrez: 29 5 2023
Statut: epublish

Résumé

Childhood lymphoma survivors (CLSs) are at high risk of reduced daily activity. This work studied metabolic substrate use and cardiorespiratory function in response to exercise in CLSs. Twenty CLSs and 20 healthy adult controls matched for sex, age, and BMI took an incremental submaximal exercise test to determine fat/carbohydrate oxidation rates. Resting echocardiography and pulmonary functional tests were performed. Physical activity level, and blood metabolic and hormonal levels were measured. CLSs reported more physical activity than controls (6317 ± 3815 vs. 4268 ± 4354 MET-minutes/week, p = 0.013), had higher resting heart rate (83 ± 14 vs. 71 ± 13 bpm, p = 0.006), and showed altered global longitudinal strain (- 17.5 ± 2.1 vs. - 19.8 ± 1.6%, p = 0.003). We observed no difference in maximal fat oxidation between the groups, but it was reached at lower relative exercise intensities in CLSs (Fatmax 17.4 ± 6.0 vs. 20.1 ± 4.1 mL/kg, p = 0.021). At V̇O CLSs reported higher levels of physical activity but they attained maximal fat oxidation at lower relative oxygen uptake and applied lower relative power at V̇O

Identifiants

pubmed: 37247034
doi: 10.1007/s00520-023-07812-5
pii: 10.1007/s00520-023-07812-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

358

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Alexandre Armand (A)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France. aarmand@chu-clermontferrand.fr.
Unité CRECHE (INSERM CIC1405), Université Clermont Auvergne, 63000, Clermont-Ferrand, France. aarmand@chu-clermontferrand.fr.

Emmanuelle Rochette (E)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.
Unité CRECHE (INSERM CIC1405), Université Clermont Auvergne, 63000, Clermont-Ferrand, France.
Université de Toulon, Laboratoire IAPS, 83041, Toulon, France.

Victoria Grèze (V)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.
Unité CRECHE (INSERM CIC1405), Université Clermont Auvergne, 63000, Clermont-Ferrand, France.

Severine Monzy (S)

Pôle Santé République, 63000, Clermont-Ferrand, France.

Christian Dualé (C)

CHU Clermont-Ferrand, Plateforme d'Investigation Clinique (INSERM CIC1405), F-63000, Clermont-Ferrand, France.

Bruno Pereira (B)

CHU Clermont-Ferrand, Délégation de La Recherche Clinique Et Innovations, 63000, Clermont-Ferrand, France.

Florentina Isfan (F)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.

Eric Doré (E)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.

Pauline Girard-Monin (P)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.

Charline Pegon (C)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.

Emmanuelle Labraise (E)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.
Unité CRECHE (INSERM CIC1405), Université Clermont Auvergne, 63000, Clermont-Ferrand, France.

Pascale Duché (P)

Université de Toulon, Laboratoire IAPS, 83041, Toulon, France.

Justyna Kanold (J)

CHU Clermont-Ferrand, Pédiatrie, 63000, Clermont-Ferrand, France.
Unité CRECHE (INSERM CIC1405), Université Clermont Auvergne, 63000, Clermont-Ferrand, France.

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