Skeletal muscle properties in long COVID and ME/CFS differ from those induced by bed rest

Abstract Patients with long COVID and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suffer from a reduced exercise capacity, skeletal muscle abnormalities and post-exertional malaise (PEM), where symptoms worsen with cognitive or physical exertion. PEM often results in avoidance of physical activity, resulting in a lower aerobic fitness, which may contribute to skeletal muscle abnormalities. Here, we compared whole-body exercise responses and skeletal muscle adaptations after strict 60-day bed rest in healthy people with those in patients with long COVID and ME/CFS, and healthy age- and sex-matched controls. Bed rest altered the respiratory and cardiovascular responses to (sub)maximal exercise, while patients exhibited respiratory alterations only at submaximal exercise. Bed rest caused muscle atrophy, and the reduced oxidative phosphorylation related to reductions in maximal oxygen uptake. Patients with long COVID and ME/CFS did not have muscle atrophy, but had less capillaries and a more glycolytic fibers, none of which were associated with maximal oxygen uptake. While the whole-body aerobic capacity is similar following bed rest compared to patients, the skeletal muscle characteristics differed, suggesting that physical inactivity alone does not explain the lower exercise capacity in long COVID and ME/CFS.

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Publication Details

Journal
Nature Communications
Published
2026-07-28
DOI
https://doi.org/10.1038/s41467-026-75725-y
Citations
2
Primary Topic
Long-Term Effects of COVID-19
Type
article
Field-Weighted Citation Impact
8.04

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article

Skeletal muscle properties in long COVID and ME/CFS differ from those induced by bed rest

Wendy Noort, Brent Appelman, Michèle van Vugt, Richie P. Goulding et al.
2 citations
Nature Communications
Long-Term Effects of COVID-19
8.04
article

Skeletal muscle properties in long COVID and ME/CFS differ from those induced by bed rest

Wendy Noort, Brent Appelman, Michèle van Vugt, Richie P. Goulding, Paul W. Hendrickse, Paul van Amstel, Hans Degens, Rob C. I. Wüst, Braeden T. Charlton, Frank W. Bloemers, Richard T. Jaspers, Moritz Eggelbusch, Anouk Slaghekke, Jelle Y Huijts, Jelle J Posthuma
article en
2 citations

Abstract

Abstract Patients with long COVID and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suffer from a reduced exercise capacity, skeletal muscle abnormalities and post-exertional malaise (PEM), where symptoms worsen with cognitive or physical exertion. PEM often results in avoidance of physical activity, resulting in a lower aerobic fitness, which may contribute to skeletal muscle abnormalities. Here, we compared whole-body exercise responses and skeletal muscle adaptations after strict 60-day bed rest in healthy people with those in patients with long COVID and ME/CFS, and healthy age- and sex-matched controls. Bed rest altered the respiratory and cardiovascular responses to (sub)maximal exercise, while patients exhibited respiratory alterations only at submaximal exercise. Bed rest caused muscle atrophy, and the reduced oxidative phosphorylation related to reductions in maximal oxygen uptake. Patients with long COVID and ME/CFS did not have muscle atrophy, but had less capillaries and a more glycolytic fibers, none of which were associated with maximal oxygen uptake. While the whole-body aerobic capacity is similar following bed rest compared to patients, the skeletal muscle characteristics differed, suggesting that physical inactivity alone does not explain the lower exercise capacity in long COVID and ME/CFS.

Nature Communications
Manchester Metropolitan University (GB), Lithuanian Sports University (LT), Flevoziekenhuis (NL), Amsterdam University Medical Centers (NL), Technical University of Munich (DE), Lancaster University (GB), Vrije Universiteit Amsterdam (NL), University of Amsterdam (NL)
National Aeronautics and Space Administration, European Space Agency, Deutsche Forschungsgemeinschaft, ZonMw
Openalex Percentile: Top 8%
Long-Term Effects of COVID-19
8.04
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