Evidence map›Paper›PMID 37940962›Full record

ReviewMolecular neurodegeneration2023

Peptide-based approaches to directly target alpha-synuclein in Parkinson's disease.

Scott G Allen, Richard M Meade, Lucy L White Stenner, Jody M Mason

Open access · goldAbstract readReview
In one paragraph

Review in Molecular neurodegeneration, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

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  15. The role of amphipathic and cationic helical peptides in Parkinson's disease.Protein science : a publication of the Protein Society · 2025
    Review
  16. Article
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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 1 institution in 1 country.

Scott G AllenDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Richard M MeadeDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Lucy L White StennerDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Jody M MasonDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK. j.mason@bath.ac.uk.
University of Bath · GB

Funding

Alzheimer's Research UK ARUK-PG2018-003BBSRC BB/T008741/1
6 · The paper itself

Abstract

Peptides and their mimetics are increasingly recognised as drug-like molecules, particularly for intracellular protein-protein interactions too large for inhibition by small molecules, and inaccessible to larger biologics. In the past two decades, evidence associating the misfolding and aggregation of alpha-synuclein strongly implicates this protein in disease onset and progression of Parkinson's disease and related synucleinopathies. The subsequent formation of toxic, intracellular, Lewy body deposits, in which alpha-synuclein is a major component, is a key diagnostic hallmark of the disease. To reach their therapeutic site of action, peptides must both cross the blood-brain barrier and enter dopaminergic neurons to prevent the formation of these intracellular inclusions. In this review, we describe and summarise the current efforts made in the development of peptides and their mimetics to directly engage with alpha-synuclein with the intention of modulating aggregation, and importantly, toxicity. This is a rapidly expanding field with great socioeconomic impact; these molecules harbour significant promise as therapeutics, or as early biomarkers during prodromal disease stages, or both. As these are age-dependent conditions, an increasing global life expectancy means disease prevalence is rising. No current treatments exist to either prevent or slow disease progression. It is therefore crucial that drugs are developed for these conditions before health care and social care capacities become overrun.

Indexed as

Parkinson DiseaseSynucleinopathiesalpha-SynucleinHumansInclusion BodiesPeptidesalpha-SynucleinPeptidesAlpha-SynucleinParkinson’s DiseasePeptide therapeuticsPeptidomimeticsSynucleinopathies

Identifiers

PMID37940962
PMCPMC10633918
OpenAlexW4388510047

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.