Evidence map›Paper›PMID 31794435›Full record

Trial reportThe Journal of clinical investigation2020

Neuromuscular junctions are stable in patients with cancer cachexia.

Ines Boehm, Janice Miller, Thomas M Wishart, Stephen J Wigmore, Richard Je Skipworth, Ross A Jones, Thomas H Gillingwater

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.2field-weighted citation impact, top 5% of its field
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

47 citing papers in PubMed, 58 citations in OpenAlex.

  1. Muscle fibre denervation in ageing.Clinical science (London, England : 1979) · 2026
    Review
  2. 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
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Physical Activity, Exerkines, and Their Role in Cancer Cachexia.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Skeletal muscle dysfunction with advancing age.Clinical science (London, England : 1979) · 2024
    Review
  20. Review
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

7 authors at 3 institutions in 1 country.

Ines BoehmBiomedical Sciences, Edinburgh Medical School, Edinburgh, United Kingdom.
Janice MillerClinical Surgery, Edinburgh Medical School and Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Thomas M WishartRoslin Institute, University of Edinburgh, Easter Bush Campus, Midlothian, United Kingdom.
Stephen J WigmoreClinical Surgery, Edinburgh Medical School and Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Richard Je SkipworthClinical Surgery, Edinburgh Medical School and Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Ross A JonesBiomedical Sciences, Edinburgh Medical School, Edinburgh, United Kingdom.
Thomas H GillingwaterBiomedical Sciences, Edinburgh Medical School, Edinburgh, United Kingdom.
Edinburgh Royal Infirmary · GBMedical Research Scotland · GBRoslin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/D/20251969Biotechnology and Biological Sciences Research Council ISPG/1 18-22Biotechnology and Biological Sciences Research Council ISPG/5 12-17Cancer Research UKChief Scientist OfficeMotor Neurone Disease Association RIBCHESTER/APR15/838-791
6 · The paper itself

Abstract

Cancer cachexia is a major cause of patient morbidity and mortality, with no efficacious treatment or management strategy. Despite cachexia sharing pathophysiological features with a number of neuromuscular wasting conditions, including age-related sarcopenia, the mechanisms underlying cachexia remain poorly understood. Studies of related conditions suggest that pathological targeting of the neuromuscular junction (NMJ) may play a key role in cachexia, but this has yet to be investigated in human patients. Here, high-resolution morphological analyses were undertaken on NMJs of rectus abdominis obtained from patients undergoing upper GI cancer surgery compared with controls (N = 30; n = 1,165 NMJs). Cancer patients included those with cachexia and weight-stable disease. Despite the low skeletal muscle index and significant muscle fiber atrophy (P < 0.0001) in patients with cachexia, NMJ morphology was fully conserved. No significant differences were observed in any of the pre- and postsynaptic variables measured. We conclude that NMJs remain structurally intact in rectus abdominis in both cancer and cachexia, suggesting that denervation of skeletal muscle is not a major driver of pathogenesis. The absence of NMJ pathology is in stark contrast to what is found in related conditions, such as age-related sarcopenia, and supports the hypothesis that intrinsic changes within skeletal muscle, independent of any changes in motor neurons, represent the primary locus of neuromuscular pathology in cancer cachexia.

Indexed as

CachexiaGastrointestinal NeoplasmsNeuromuscular JunctionRectus AbdominisFemaleHumansMaleNeuromuscular diseaseNeuroscienceOncology

Identifiers

PMID31794435
PMCPMC7269586
OpenAlexW2992512203

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.