Evidence map›Paper›PMID 33786805›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2021

Specific Expression of Glial-Derived Neurotrophic Factor in Muscles as Gene Therapy Strategy for Amyotrophic Lateral Sclerosis.

Guillem Mòdol-Caballero, Belén García-Lareu, Mireia Herrando-Grabulosa, Sergi Verdés, Rubén López-Vales, Gemma Pagès, Miguel Chillón, Xavier Navarro, Assumpció Bosch

Open access · bronzeAbstract read
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Skeletal muscle dysfunction in amyotrophic lateral sclerosis: a mitochondrial perspective and therapeutic approaches.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Review
  7. Article
  8. Skeletal muscle in amyotrophic lateral sclerosis.Brain : a journal of neurology · 2023
    Review
  9. Review
  10. Approaches to Gene Modulation Therapy for ALS.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  11. Review
  12. Article
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 2 institutions in 1 country.

Guillem Mòdol-Caballero *Institute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Belén García-LareuInstitute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Mireia Herrando-Grabulosa *Institute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Sergi VerdésInstitute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Rubén López-ValesInstitute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Gemma PagèsDepartment of Biochemistry and Molecular Biology, Universitat Autònoma de Barcelona, Barcelona, Spain.
Miguel ChillónInstitute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Xavier NavarroInstitute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain. xavier.navarro@uab.cat.
Assumpció BoschInstitute of Neurosciences, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain. assumpcio.bosch@uab.cat.ORCID http://orcid.org/0000-0002-7205-2796
Universitat Autònoma de Barcelona · ESInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glial cell line-derived neurotrophic factor (GDNF) is a powerful neuroprotective growth factor. However, systemic or intrathecal administration of GDNF is associated with side effects. Here, we aimed to avoid this by restricting the transgene expression to the skeletal muscle by gene therapy. To specifically target most skeletal muscles in the mouse model of amyotrophic lateral sclerosis (ALS), SOD1

Indexed as

Amyotrophic Lateral SclerosisAnimalsFemaleGene ExpressionGenetic TherapyGlial Cell Line-Derived Neurotrophic FactorHEK293 CellsHumansMaleMiceMice, Inbred C57BLMice, TransgenicMuscle, SkeletalSuperoxide DismutaseGdnf protein, mouseGlial Cell Line-Derived Neurotrophic FactorSOD1 G93A proteinSuperoxide DismutaseAAVAmyotrophic lateral sclerosisGDNFGene therapyMotoneuronNeuromuscular junction

Identifiers

PMID33786805
PMCPMC8423878
OpenAlexW3147537077

What OpenQuestion holds

Textmetadata
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.