Evidence map›Paper›PMID 41757086›Full record

ArticlebioRxiv : the preprint server for biology2026

Multilevel impairment of mitochondrial respiration with sex-specific signatures in inclusion body myositis.

Ibrahim Shammas, Hazem Iaali, Jens O Watzlawik, Noemi Vidal Folch, Surendra Dasari, Graeme Preston, Thi Kim Oanh Nguyen, Wolfdieter Springer, Tamas Kozicz, Linda Hasadsri and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Ibrahim ShammasDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Hazem IaaliDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Jens O WatzlawikDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Noemi Vidal FolchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Surendra DasariDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Graeme PrestonDepartment of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
Thi Kim Oanh NguyenDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Wolfdieter SpringerDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Tamas KoziczDepartment of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
Linda HasadsriDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Eugenia TrushinaDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Ian R LanzaDivision of Endocrinology, Nutrition, and Metabolism, Mayo Clinic, Rochester, MN, USA.
Elie NaddafDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.

Funding

Mayo Clinic Center for Clinical and Translational Science (CCaTS UL1 Supplement - Dr. Timothy Curry)UL1TR002377 · NCATS · MAYO CLINIC ROCHESTER · PI VESNA D GAROVIC · 2017 to 2026
$78.4M
Mitochondrial Complex I as a Target for Neuroprotection in ADRF1AG055549 · NIA · MAYO CLINIC ROCHESTER · PI TRUSHINA, EUGENIA · 2017 to 2025
$7.0M
Molecular mechanisms of PINK1-PRKN directed mitochondrial quality controlRF1NS085070 · NINDS · MAYO CLINIC JACKSONVILLE · PI SPRINGER, WOLFDIETER · 2019 to 2019
$2.8M
The Role of Mitochondria in Inclusion Body MyositisK08AR078254 · NIAMS · MAYO CLINIC ROCHESTER · PI NADDAF, ELIE · 2021 to 2025
$815k
NCATS NIH HHS UL1 TR002377NIAMS NIH HHS K08 AR078254NIA NIH HHS RF1 AG055549NINDS NIH HHS RF1 NS085070
6 · The paper itself

Abstract

Background: Oxidative phosphorylation (OXPHOS) is a central function and a key indicator of mitochondrial fitness, yet studies in human tissue remain limited. Inclusion body myositis (IBM) is a progressive myopathy that lies at the intersection of aging, inflammation and mitochondrial dysfunction. We aimed to perform a comprehensive profiling of mitochondrial respiration in muscle tissue from patients with IBM. Methods: A wide battery of complementary tests from RNA level to high-resolution respirometry on permeabilized muscle fibers was performed. The relationship between respiration, mitochondrial content, mitochondrial DNA (mtDNA) abnormalities and mitophagy was examined, along with the correlation with various clinical parameters to determine the clinical significance of the findings. Results: The study included a total of 67 patients with IBM and 45 controls. IBM muscle tissue exhibited reduced maximal respiration per tissue weight in State 3 (high substrates, high ADP) and uncoupled state with decreased coupling efficiency and higher leak control ratios. When adjusting for citrate synthase reflecting mitochondrial content, males had decreased State 3 intrinsic respiration, whereas females had greater intrinsic respiration in leak states. Complex II control ratio strongly correlated with disease duration and severity only in females. IBM was associated with decreased RNA and protein expression of OXPHOS complexes. Complex I activity was decreased mainly in females. IBM samples exhibited lower maximal H Conclusion: IBM is characterized by multilevel impairments in mitochondrial coupling efficiency, revealing several potential therapeutic targets to improve mitochondrial fitness, while accounting for sex-specific differences.

Indexed as

agingmitochondrial DNA abnormalitiesmitophagymyopathyoxidative phosphorylationoxidative stress

Identifiers

PMID41757086
PMCPMC12934724

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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.