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Effect of high-intensity interval training in patients with chronic hepatitis B and hepatic steatosis: A randomised controlled trial

  • Sofie Jespersen*
  • , Asmita Fritt-Rasmussen
  • , Cody Garett Durrer
  • , Eva Fallentin
  • , Ellen Sloth Andersen
  • , Peter Thielsen
  • , Thomas Bandholm
  • , Sten Madsbad
  • , Bente Klarlund Pedersen
  • , Christian Ritz
  • , Nina Weis
  • , Rikke Krogh-Madsen
  • *Kontaktforfatter
  • Rigshospitalet
  • Københavns Universitetshospital
  • Københavns Universitet

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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Abstract

Background & aims 

Having both chronic hepatitis B and hepatic steatosis increases the risk of liver-related morbidity and mortality. We aimed to investigate if high-intensity interval training could decrease the liver fat-fraction and improve liver status, body composition, lipid- and glucose metabolism, and blood pressure in patients with chronic hepatitis B and hepatic steatosis. 


Methods 

In a randomised, controlled trial, patients with chronic hepatitis B and hepatic steatosis were randomised 1:1 to high-intensity interval training over 12 weeks or no intervention. The primary outcome was reduction in liver fat-fraction (≥ 2.8%), assessed by magnetic resonance imaging. Secondary outcomes were body composition, indices of glucose metabolism, blood lipids, blood pressure, alanine aminotransferase, physical fitness assessed by maximal oxygen consumption (VO2max), and self-assessed health. The trial was discontinued before reaching the planned sample size due to slow recruitment. 


Results 

Nineteen patients were included, and 14 completed the trial (seven per group). Changes in liver fat-fraction showed a between-group difference of −2.03% [95% CI: −5.5 to 1.4; p = 0.22]. Exercising patients improved VO2max by 5.6 mL/kg/min [1.7 to 9.5; p < 0.05] and emotional well-being by 18.07 points [6.6 to 29.6; p < 0.05]. The exercise intervention did not affect total body fat −0.35% [−2.8 to 2.1] or lean body mass 0.6 kg [−0.7 to 1.9]. Changes in glucose tolerance, insulin secretion, Matsuda index −0.89 [−2.5 to 0.5; p = 0.18], cholesterol 0.29 mmol/L [−0.3 to 0.9; p = 0.32] and systolic blood pressure 6.36 mmHg [−6.4 to 19.1; p = 0.29] did not differ significantly between groups. 


Conclusions 

We did not observe a significant effect of high-intensity interval training on liver fat-fraction in patients with chronic hepatitis B and hepatic steatosis. Due to premature discontinuation and the resulting limited sample size, the study was underpowered, and the findings should be interpreted as exploratory. Nevertheless, the intervention improved physical fitness and emotional well-being.

OriginalsprogEngelsk
Artikelnummere0351547
TidsskriftPLOS ONE
Vol/bind21
Udgave nummer6
Antal sider17
ISSN1932-6203
DOI
StatusUdgivet - jun. 2026

Finansiering

The Center for Physical Activity Research is supported by TrygFonden (grants ID 101390 580 and ID 20045). The study was supported by the Department of Infectious Diseases, Copenhagen University Hospiutal, Hvidovre. Furthermore, this study was supported by the Beckett Foundation (ref. no: 22-2-9924) with a grant to SJ. The grant supporters had no role in the planning, execution, or data analysis of the study. We humbly thank all patients involved in the study for their time and participation. We thank Katja Kofoed and Emil Nelander Schmidt for project coordination and assistance in carrying out the study; we thank the students (Frederik Hammerich, Jon Dissing Sund, Mathilde Nicolaisen) for performing the exercise sessions and the staff at the Center for Physical Activity Research for their assistance in conducting the examinations of the patients. We thank the Department of Infectious Diseases staff at Copenhagen University Hospital, Hvidovre, for assisting with patient recruitment and transient elastography. We thank the Danish National Institute of Public Health, the University of Southern Denmark, and TrygFonden for lending us the activity trackers for this project. We thank the RAND as a part of the Medical Outcome Study for the use of the 36-item Health Survey.

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