Evidence mapPaperPMID 39362957Full record

ArticleScientific reports2024

Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic study.

Alexander Schaiter, Andreas Hentschel, Felix Kleefeld, Julia Schuld, Vincent Umathum, Tara Procida-Kowalski, Christopher Nelke, Angela Roth, Andreas Hahn, Heidrun H Krämer and 6 more

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

16 authors.

Alexander SchaiterInstitute of Neuropathology, Justus-Liebig University, Giessen, Germany.
Andreas HentschelLeibnitz Institut für Analytische Wissenschaften-ISAS e.V., Dortmund, Germany.
Felix KleefeldDepartment of Clinical Neurosciences, School of Clinical Medicine, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, UK.
Julia SchuldDepartment of Molecular Cell Biology, Institute for Cell Biology, University of Bonn, Bonn, Germany.
Vincent UmathumInstitute of Neuropathology, Justus-Liebig University, Giessen, Germany.
Tara Procida-KowalskiInstitute for Lung Health (ILH), Justus-Liebig University, Giessen, Germany.
Christopher NelkeDepartment of Neurology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Angela RothInstitute of Neuropathology, Justus-Liebig University, Giessen, Germany.
Andreas HahnDepartment of Pediatric Neurology, Justus-Liebig University Giessen, Giessen, Germany.
Heidrun H KrämerDepartment of Neurology, Justus-Liebig University Giessen, Giessen, Germany.
Tobias RuckDepartment of Neurology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Rita HorvathDepartment of Clinical Neurosciences, School of Clinical Medicine, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, UK.
Peter F M van der VenDepartment of Molecular Cell Biology, Institute for Cell Biology, University of Bonn, Bonn, Germany.
Marek Bartkuhn *Institute for Lung Health (ILH), Justus-Liebig University, Giessen, Germany.
Andreas Roos *Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, Essen, Germany.
Anne Schänzer *Institute of Neuropathology, Justus-Liebig University, Giessen, Germany. anne.schaenzer@patho.med.uni-giessen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To gain a deeper understanding of skeletal muscle function in younger age and aging in elderly, identification of molecular signatures regulating these functions under physiological conditions is needed. Although molecular studies of healthy muscle have been conducted on adults and older subjects, there is a lack of research on infant muscle in terms of combined morphological, transcriptomic and proteomic profiles. To address this gap of knowledge, we performed RNA sequencing (RNA-seq), tandem mass spectrometry (LC-MS/MS), morphometric analysis and assays for mitochondrial maintenance in skeletal muscle biopsies from both, infants aged 4-28 months and adults aged 19-65 years. We identified differently expressed genes (DEGs) and differentially expressed proteins (DEPs) in adults compared to infants. The down-regulated genes in adults were associated with functional terms primarily related to sarcomeres, cellular maintenance, and metabolic, immunological and developmental processes. Thus, our study indicates age-related differences in the molecular signatures and associated functions of healthy skeletal muscle. Moreover, the findings assert that processes previously associated solely with aging are indeed part of development and healthy aging. Hence, combined findings of this study also indicate that age-dependent controls are crucial in muscle disease studies, as otherwise the comparative results may not be reliable.

Indexed as

Muscle, SkeletalProteomicsTranscriptomeAdultAgedAgingFemaleGene Expression ProfilingHumansInfantMaleMiddle AgedProteomeTandem Mass SpectrometryYoung AdultProteomeBioinformatics in omicsMitochondria in agingMuscle proteomicsMuscle transcriptomics

Identifiers

PMID39362957
PMCPMC11450201

What Socratic holds

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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 Socratic graph.