Evidence map›Paper›PMID 39236304›Full record

ArticleJournal of cachexia, sarcopenia and muscle2024

Neuromuscular impairment at different stages of human sarcopenia.

Fabio Sarto, Martino V Franchi, Jamie S McPhee, Daniel W Stashuk, Matteo Paganini, Elena Monti, Maira Rossi, Giuseppe Sirago, Sandra Zampieri, Evgeniia S Motanova and 8 more

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
–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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  10. Muscle fibre denervation in ageing.Clinical science (London, England : 1979) · 2026
    Review
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  14. Junctions in Jeopardy: the neuromuscular junction is a selective pathological target in Charcot-Marie-Tooth disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  15. Article
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  18. Does Time Tick Faster in Cerebral Palsy? Accelerated Aging as a Framework for Skeletal Muscle Dysfunction.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
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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

18 authors.

Fabio SartoDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID 0000-0001-8572-5147
Martino V FranchiDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Jamie S McPheeDepartment of Sport and Exercise Sciences, Manchester Metropolitan University Institute of Sport, Manchester, UK.
Daniel W StashukDepartment of Systems Design Engineering, University of Waterloo, Waterloo, ON, Canada.
Matteo PaganiniDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Elena MontiBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Maira RossiInstitute of Physiology, Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Giuseppe SiragoDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Sandra ZampieriDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Evgeniia S MotanovaDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Giacomo ValliDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Tatiana MoroDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Antonio PaoliDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Roberto BottinelliInstitute of Physiology, Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Maria A PellegrinoInstitute of Physiology, Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Giuseppe De VitoDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Helen M BlauBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Marco V NariciDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID 0000-0003-0167-1845

Funding

Donald E. and Delia B. Baxter FoundationLi Ka Shing FoundationNeuAge 2017CBF8NJ_001Next Generation EU DM 1557Stanford Wu Tsai Human Performance Institute Fellowship
6 · The paper itself

Abstract

backgroundDegeneration of the motoneuron and neuromuscular junction (NMJ) and loss of motor units (MUs) contribute to age-related muscle wasting and weakness associated with sarcopenia. However, these features have not been comprehensively investigated in humans. This study aimed to compare neuromuscular system integrity and function at different stages of sarcopenia, with a particular focus on NMJ stability and MU properties.

methodsWe recruited 42 young individuals (Y) (aged 25.98 ± 4.6 years; 57% females) and 88 older individuals (aged 75.9 ± 4.7 years; 55% females). The older group underwent a sarcopenia screening according to the revised guidelines of the European Working Group on Sarcopenia in Older People 2. In all groups, knee extensor muscle force was evaluated by isometric dynamometry, muscle morphology by ultrasound and MU potential properties by intramuscular electromyography (iEMG). MU number estimate (iMUNE) and blood samples were obtained. Muscle biopsies were collected in a subgroup of 16 Y and 52 older participants.

resultsThirty-nine older individuals were non-sarcopenic (NS), 31 pre-sarcopenic (PS) and 18 sarcopenic (S). A gradual decrease in quadriceps force, cross-sectional area and appendicular lean mass was observed across the different stages of sarcopenia (for all P < 0.0001). Handgrip force and the Short Physical Performance Battery score also showed a diminishing trend. iEMG analyses revealed elevated near fibre segment jitter in NS, PS and S compared with Y (Y vs. NS and S: P < 0.0001; Y vs. PS: P = 0.0169), suggestive of age-related impaired NMJ transmission. Increased C-terminal agrin fragment (P < 0.0001) and altered caveolin 3 protein expression were consistent with age-related NMJ instability in all the older groups. The iMUNE was lower in all older groups (P < 0.0001), confirming age-related loss of MUs. An age-related increase in MU potential complexity was also observed. These observations were accompanied by increased muscle denervation and axonal damage, evinced by the increase in neural cell adhesion molecule-positive fibres (Y vs. NS: P < 0.0001; Y vs. S: P = 0.02) and the increase in serum concentration of neurofilament light chain (P < 0.0001), respectively. Notably, most of these MU and NMJ parameters did not differ when comparing older individuals with or without sarcopenia.

conclusionsAlterations in MU properties, axonal damage, an altered innervation profile and NMJ instability are prominent features of the ageing of the neuromuscular system. These neuromuscular alterations are accompanied by muscle wasting and weakness; however, they appear to precede clinically diagnosed sarcopenia, as they are already detectable in older NS individuals.

Indexed as

SarcopeniaAdultAgedAged, 80 and overElectromyographyFemaleHumansMaleMuscle, SkeletalNeuromuscular JunctionYoung Adultelectromyographyfibre denervationmotoneuronmotor unitsmuscle atrophyneuromuscular junction

Identifiers

PMID39236304
PMCPMC11446718

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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.