Evidence map›Paper›PMID 33809527›Full record

ReviewCells2021

Mechanisms of Neurodegeneration in Various Forms of Parkinsonism-Similarities and Differences.

Dariusz Koziorowski, Monika Figura, Łukasz M Milanowski, Stanisław Szlufik, Piotr Alster, Natalia Madetko, Andrzej Friedman

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. The Role of MicroRNAs in Progressive Supranuclear Palsy-A Systematic Review.International journal of molecular sciences · 2024
    Pooled it
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  16. Asymmetry in Atypical Parkinsonian Syndromes-A Review.Journal of clinical medicine · 2024
    Review
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  18. 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

7 authors at 1 institution in 2 countries.

Dariusz KoziorowskiDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.ORCID 0000-0001-8920-8024
Monika FiguraDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.
Łukasz M MilanowskiDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.ORCID 0000-0003-4197-8518
Stanisław SzlufikDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.
Piotr AlsterDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.ORCID 0000-0002-5371-6817
Natalia MadetkoDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.
Andrzej FriedmanDepartment of Neurology, Faculty of Heath Science, Medical University of Warsaw, 03-285 Warsaw, Poland.
Medical University of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD), dementia with Lewy body (DLB), progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and multiple system atrophy (MSA) belong to a group of neurodegenerative diseases called parkinsonian syndromes. They share several clinical, neuropathological and genetic features. Neurodegenerative diseases are characterized by the progressive dysfunction of specific populations of neurons, determining clinical presentation. Neuronal loss is associated with extra- and intracellular accumulation of misfolded proteins. The parkinsonian diseases affect distinct areas of the brain. PD and MSA belong to a group of synucleinopathies that are characterized by the presence of fibrillary aggregates of α-synuclein protein in the cytoplasm of selected populations of neurons and glial cells. PSP is a tauopathy associated with the pathological aggregation of the microtubule associated tau protein. Although PD is common in the world's aging population and has been extensively studied, the exact mechanisms of the neurodegeneration are still not fully understood. Growing evidence indicates that parkinsonian disorders to some extent share a genetic background, with two key components identified so far: the microtubule associated tau protein gene (

Indexed as

Nerve Degenerationalpha-SynucleinAnimalsBrainGenetic Predisposition to DiseaseHumansMitochondriaMitophagyNeuronsOxidative StressParkinsonian DisordersPhenotypeRisk Factorstau Proteinsalpha-SynucleinMAPT protein, humanSNCA protein, humantau ProteinsDLBMAPTmitophagyMSAneurodegenerationoxidative stressPDPSPSNCA

Identifiers

PMID33809527
PMCPMC7999195
OpenAlexW3139476025

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.