Evidence map›Paper›PMID 34328594›Full record

ReviewGlycoconjugate journal2022

Innovative treatment targeting gangliosides aimed at blocking the formation of neurotoxic α-synuclein oligomers in Parkinson's disease.

Nouara Yahi, Coralie Di Scala, Henri Chahinian, Jacques Fantini

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Glycoconjugate journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

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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

4 authors at 3 institutions in 2 countries.

Nouara YahiINSERM UMR_S 1072, Aix-Marseille Université, 13015, Marseille, France.
Coralie Di ScalaNeuroscience Center-HiLIFE, University of Helsinki, 00014, Helsinki, Finland.
Henri ChahinianINSERM UMR_S 1072, Aix-Marseille Université, 13015, Marseille, France.
Jacques FantiniINSERM UMR_S 1072, Aix-Marseille Université, 13015, Marseille, France. jm.fantini@gmail.com.
Aix-Marseille Université · FRInserm · FRUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a major neurodegenerative disorder which exhibits many of the characteristics of a pandemic. Current therapeutic strategies are centered on the dopaminergic system, with limited efficacy, so that a treatment that has a direct impact on the underlying disease pathogenesis is urgently needed. Although α-synuclein is a privileged target for such therapies, this protein has been in the past wrongly considered as exclusively intracellular, so that the impact of paracrine neurotoxicity mechanisms in PD have been largely ignored. In this article we review the data showing that lipid rafts act as plasma membrane machineries for the formation of α-synuclein pore-like oligomers which trigger an increase of intracellular Ca

Indexed as

alpha-SynucleinParkinson DiseaseDisease ProgressionGangliosidesHumansMembrane Microdomainsalpha-SynucleinGangliosidesAmyloid poreCholesterolGangliosideLipid raftNeurodegenerative diseaseTreatment

Identifiers

PMID34328594
OpenAlexW3185395844

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.