Evidence map›Paper›PMID 37317638›Full record

ArticleNeuropathology and applied neurobiology2023

Treatment with the copper compound CuATSM has no significant effect on motor neuronal pathology in patients with ALS.

Yue Yang, Dominic Rowe, Heather McCann, Claire E Shepherd, Jillian J Kril, Matthew C Kiernan, Glenda M Halliday, Rachel H Tan

Open access · hybridAbstract read
In one paragraph

Article in Neuropathology and applied neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Recent progress of methods for cuproptosis detection.Frontiers in molecular biosciences · 2024
    Review
  10. Ferroptosis inhibitors: past, present and future.Frontiers in pharmacology · 2024
    Review
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

  • Commented on by
    Cu2023
5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Yue YangBrain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
Dominic RoweMacquarie University Centre for Motor Neuron Disease Research, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, New South Wales, Australia.
Heather McCannNeuroscience Research Australia, Randwick, New South Wales, Australia.
Claire E ShepherdNeuroscience Research Australia, Randwick, New South Wales, Australia.ORCID 0000-0002-0399-3218
Jillian J KrilFaculty of Medicine and Health, School of Medical Sciences, University of Sydney, Camperdown, New South Wales, Australia.ORCID 0000-0001-9407-8674
Matthew C KiernanBrain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
Glenda M HallidayBrain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID 0000-0003-0422-8398
Rachel H TanBrain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.ORCID 0000-0002-0385-4090
The University of Sydney · AUNeuroscience Research Australia · AUMacquarie University · AU

Funding

Brain Tissue Resource Centre for Alcohol ResearchR28AA012725 · NIAAA · UNIVERSITY OF SYDNEY · PI Greg Trevor Sutherland · 2012 to 2026
$7.0M
NIAAA NIH HHS R28 AA012725
6 · The paper itself

Abstract

aimsAlthough the orally available brain-penetrant copper compound CuATSM has demonstrated promising effects in SOD1-linked mouse models, the impact of CuATSM on disease pathology in patients with amyotrophic lateral sclerosis (ALS) remains unknown.

methodsThe present study set out to address this deficit by performing the first pilot comparative analysis of ALS pathology in patients that had been administered CuATSM and riluzole [N = 6 cases composed of ALS-TDP (n = 5) and ALS-SOD1 (n = 1)] versus riluzole only [N = 6 cases composed of ALS-TDP (n = 4) and ALS-SOD1 (n = 2)].

resultsOur results revealed no significant difference in neuron density or TDP-43 burden in the motor cortex and spinal cord of patients that had received CuATSM compared with patients that had not. In patients that had received CuATSM, p62-immunoreactive astrocytes were observed in the motor cortex and reduced Iba1 density was found in the spinal cord. However, no significant difference in measures of astrocytic activity and SOD1 immunoreactivity was found with CuATSM treatment. DISCUSSION: These findings, in this first postmortem investigation of patients with ALS in CuATSM trials, demonstrate that in contrast to that seen in preclinical models of disease, CuATSM does not significantly alleviate neuronal pathology or astrogliosis in patients with ALS.

Indexed as

Amyotrophic Lateral SclerosisAnimalsCopperDNA-Binding ProteinsMiceMice, TransgenicMotor NeuronsOrganocopper CompoundsRiluzoleSpinal CordSuperoxide DismutaseSuperoxide Dismutase-1CopperCuATSMDNA-Binding ProteinsOrganocopper CompoundsRiluzoleSuperoxide DismutaseSuperoxide Dismutase-1amyotrophic lateral sclerosiscopper ATSM (CuATSM)p62 pathologyriluzoleTDP-43 pathology

Identifiers

PMID37317638
PMCPMC10947464
OpenAlexW4380730727

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.