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Investigating the circulating sphingolipidome response to a single high-intensity interval training session within healthy females and males in their twenties (SphingoHIIT): Protocol for a randomised controlled trial [version 2; peer review: 2 approved]

Authors :
Justin Carrard
Thomas Angst
Nadia Weber
Joëlle Bienvenue
Denis Infanger
Lukas Streese
Timo Hinrichs
Ilaria Croci
Christian Schmied
Hector Gallart-Ayala
Christoph Höchsmann
Karsten Koehler
Henner Hanssen
Julijana Ivanisevic
Arno Schmidt-Trucksäss
Author Affiliations :
<relatesTo>1</relatesTo>Division of Sport and Exercise Medicine, Department of Sport, Exercise and Health, University of Basel, Basel, 4052, Switzerland<br /><relatesTo>2</relatesTo>Cardiac Exercise Research Group, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway<br /><relatesTo>3</relatesTo>Sports Cardiology Section, Department of Cardiology, University Heart Center Zurich,, University Hospital Zurich, Zurich, 8091, Switzerland<br /><relatesTo>4</relatesTo>Metabolomics Platform, Faculty of Biology and Medicine, University of Lausanne, Lausanne, 1005, Switzerland<br /><relatesTo>5</relatesTo>Department of Sport and Health Sciences, Technical University of Munich, Munich, Germany
Source :
F1000Research. 11:1565
Publication Year :
2023
Publisher :
London, UK: F1000 Research Limited, 2023.

Abstract

Introduction: Growing scientific evidence indicates that sphingolipids predict cardiometabolic risk, independently of and beyond traditional biomarkers such as low-density lipoprotein cholesterol. To date, it remains largely unknown if and how exercise, a simple, low-cost, and patient-empowering modality to optimise cardiometabolic health, influences sphingolipid levels. The SphingoHIIT study aims to assess the response of circulating sphingolipid species to a single session of high-intensity interval training (HIIT). Methods: This single-centre randomised controlled trial (RCT) will last 11 days per participant and aim to include 32 young and healthy individuals aged 20-29 (50% females). Participants will be randomly allocated to the HIIT (n= 16) or control groups (physical rest, n= 16). Participants will self-sample fasted dried blood spots for three consecutive days before the intervention (HIIT versus rest) to determine baseline sphingolipid levels. Dried blood spots will also be collected at five time points (2, 15, 30, 60min, and 24h) following the intervention (HIIT versus rest). To minimise the dietary influence, participants will receive a standardised diet for four days, starting 24 hours before the first dried blood sampling. For females, interventions will be timed to fall within the early follicular phase to minimise the menstrual cycle's influence on sphingolipid levels. Finally, physical activity will be monitored for the whole study duration using a wrist accelerometer. Ethics and dissemination: The Ethics Committee of Northwest and Central Switzerland approved this protocol (ID 2022–00513). Findings will be disseminated in scientific journals and meetings. Trial Registration The trial was registered on www.clinicaltrials.gov (NCT05390866, https://clinicaltrials.gov/ct2/show/NCT05390866) on May 25, 2022.

Details

ISSN :
20461402
Volume :
11
Database :
F1000Research
Journal :
F1000Research
Notes :
Revised Amendments from Version 1 This new version addressed the comments made by the reviewer. Specifically, we provide more details about the sample size calculation (including the R code), reformulate the statistical analysis strategy according to the reviewer suggestions and acknowledge in the introduction the fact that different sphingolipids might have different biological effects depending on acyl chain length and saturation, with shorter and unsaturated species being potentially more detrimental to human health., , [version 2; peer review: 2 approved]
Publication Type :
Academic Journal
Accession number :
edsfor.10.12688.f1000research.128978.2
Document Type :
study-protocol
Full Text :
https://doi.org/10.12688/f1000research.128978.2