Evidence map›Paper›PMID 32133457›Full record

ArticleBrain communications2019

Targeting mitochondrial dysfunction in amyotrophic lateral sclerosis: a systematic review and meta-analysis.

Arpan R Mehta, Rachel Walters, Fergal M Waldron, Suvankar Pal, Bhuvaneish T Selvaraj, Malcolm R Macleod, Giles E Hardingham, Siddharthan Chandran, Jenna M Gregory

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Trimetazidine Improves Mitochondrial Dysfunction in SOD1International journal of molecular sciences · 2024
    Article
  9. Mitochondrial Inherited Disorders and their Correlation with Neurodegenerative Diseases.Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Regulation of Endoplasmic Reticulum-Mitochondria Tethering and CaInternational journal of molecular sciences · 2021
    Article
  17. Article
  18. Review
  19. Article
  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

9 authors at 5 institutions in 2 countries.

Arpan R MehtaUK Dementia Research Institute, University of Edinburgh, Edinburgh, UK.
Rachel WaltersCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Fergal M WaldronInstitute of Evolutionary Biology and Centre for Immunity Infection and Evolution, University of Edinburgh, Ashworth Laboratories, Edinburgh, UK.
Suvankar PalCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Bhuvaneish T SelvarajUK Dementia Research Institute, University of Edinburgh, Edinburgh, UK.
Malcolm R MacleodCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Giles E HardinghamUK Dementia Research Institute, University of Edinburgh, Edinburgh, UK.
Siddharthan ChandranUK Dementia Research Institute, University of Edinburgh, Edinburgh, UK.
Jenna M GregoryUK Dementia Research Institute, University of Edinburgh, Edinburgh, UK.
MRC Centre for Regenerative Medicine · GBUK Dementia Research Institute · GBCentre for Immunity, Infection and Evolution · GBInstitute for Stem Cell Biology and Regenerative Medicine · INUniversity of Oxford · GB

Funding

Medical Research Council MR/R001162/1Motor Neurone Disease Association MEHTA/JUL17/948-795
6 · The paper itself

Abstract

Interventions targeting mitochondrial dysfunction have the potential to extend survival in preclinical models of amyotrophic lateral sclerosis. The aim of this systematic review was to assess the efficacy of targeting mitochondria as a potential therapeutic target in amyotrophic lateral sclerosis. Preclinical studies written in the English language were identified with no restrictions on publication date from PubMed, Medline and EMBASE databases. All studies adopting interventions targeting mitochondria to treat amyotrophic lateral sclerosis in genetic or drug-induced organism models were considered for inclusion. A total of 76 studies were included in the analysis. Survival data were extracted, and the meta-analysis was completed in RevMan 5 software. We show that targeting mitochondrial dysfunction in amyotrophic lateral sclerosis results in a statistically significant improvement in survival (

Indexed as

amyotrophic lateral sclerosismeta-analysismitochondriamodellingsystematic review

Identifiers

PMID32133457
PMCPMC7056361
OpenAlexW2965252952

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.