Evidence map›Paper›PMID 41030235›Full record

Trial reportJournal of cachexia, sarcopenia and muscle2025

Muscle Abnormalities in Nonhospitalised Patients With Post-COVID-19 Condition.

Andrea Tryfonos, Gustav Jörnåker, Håkan Rundqvist, Kaveh Pourhamidi, Michael Melin, Helena Wallin, Filip J Larsen, Spyridon Pantelios, Anders P Mutvei, Veronika Tillander and 10 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of cachexia, sarcopenia and muscle, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05445830 (Physiological Characterization of Functional Limitations and Exercise Intolerance in Post-COVID Patients), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05445830 nacompletednot on this map

Physiological Characterization of Functional Limitations and Exercise Intolerance in Post-COVID Patients

TypeinterventionalSponsorKarolinska InstitutetRan2022 to 2025Enrolled62ConditionsPost-COVID SyndromeArmsHigh-Intensity-Interval-Exercise, Moderate-Intensity-Continuous-Exercise, Strength training, Baseline assessment, 1 year follow-up
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Andrea TryfonosDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.ORCID 0000-0002-8226-0724
Gustav JörnåkerDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Håkan RundqvistDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Kaveh PourhamidiDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Michael MelinDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Helena WallinDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Filip J LarsenDepartment of Physiology, Nutrition and Biomechanics, Swedish School of Sport and Health Sciences, GIH, Stockholm, Sweden.
Spyridon PanteliosDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Huddinge, Sweden.
Anders P MutveiDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Huddinge, Sweden.
Veronika TillanderDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institutet, Huddinge, Sweden.
Uwe J F TietgeDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institutet, Huddinge, Sweden.
Sergio Perez DiazDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Douglas CrafoordDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Alen LovricDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Rodrigo Fernandez-GonzaloDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Eric RullmanDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Per StålDepartment of Medical and Translational Biology, Umeå University, Umeå, Sweden.
Thomas GustafssonDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Helene RundqvistDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.
Tommy R LundbergDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet, Huddinge, Sweden.

Funding

Åke Wibergs Foundation 2023 M23-0178CIMED H550205553CIMED H550205763Dr Margaretha Nilssons Foundation 2024Hannover Foundation Donation via Karolinska InstitutetKI Research Foundation Grants 2024-2025 2024-02651Lars Hierta Memorial Foundation 2022 and 2023 FO2022-0034Lars Hierta Memorial Foundation 2022 and 2023 FO2023-0095Magnus Bergvalls Foundation 2022 and 2023 2022-310Magnus Bergvalls Foundation 2022 and 2023 2023-494Tore Nilsson Foundation 2023 2023-100Tornspiran Foundation 2022 814
6 · The paper itself

Abstract

backgroundPost-COVID condition (PCC) affects ~10% of SARS-CoV-2-infected individuals and manifests as persistent symptoms such as fatigue, exercise intolerance and muscle weakness. This study aimed to assess the skeletal muscle of these patients and compare them with healthy controls.

methodsBiopsies were obtained from the vastus lateralis muscle of 28 nonhospitalised PCC patients without concomitant diseases (75% women, mean age 46.4 ± 10.4 years) and 28 age- and sex-matched healthy controls (79% women, mean age 46.6 ± 8.7 years). The analysis included morphological and pathological alterations, fibre type composition, fibre cross-sectional area, capillarisation, number of myonuclei, presence of developmental myosin, CD68

resultsPCC patients, compared to controls, had a higher percentage of angulated fibres (median [IQR] 0.43 [0.00-3.20] vs. 0.00 [0.00-0.00]; p < 0.001), small, rounded fibres (0.21 [0.00-1.20] vs. 0.00 [0.00-0.00]; p < 0.001) and fibres expressing fetal myosin (0.26 [0.00-1.15] vs. 0.00 [0.00-0.17]; p = 0.015). Semiquantitative analysis showed nuclear clumps (18/27, 66.6%), hypertrophic fibres (9/27, 33.3%) and fibrosis (22/27, 81.4%) in PCC patients. Fibre cross-sectional area was significantly lower in PCC patients (4031 ± 1365 vs. 4982 ± 1463 μm

conclusionsNonhospitalised patients with PCC show signs of morphological and pathological muscle changes suggestive of degeneration and regeneration. The smaller overall fibre size, lower number of phospholipids, reduced mitochondrial oxidative capacity and lower capillarisation in these patients may be a consequence of reduced physical activity levels. The presence of clusters of atrophied angular and round-shaped fibres, signs of inflammation and fibrosis and increased expression of fetal myosin may reflect myopathic and neurogenic post-viral effects.

trial registrationClinicalTrials.gov Identifier: NCT05445830.

Indexed as

COVID-19Muscle, SkeletalMuscular DiseasesAdultBiopsyCase-Control StudiesCross-Over StudiesFemaleHumansMaleMiddle AgedMuscle Fibers, SkeletalSARS-CoV-2muscle abnormalitiesmuscle histologymyopathiespost–COVID‐19 conditionRNA sequencingskeletal muscle

Identifiers

PMID41030235
PMCPMC12485287

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.