Evidence map›Paper›PMID 25170892›Full record

ArticlePloS one2014

Systems-based analyses of brain regions functionally impacted in Parkinson's disease reveals underlying causal mechanisms.

Brigit E Riley, Shyra J Gardai, Dorothea Emig-Agius, Marina Bessarabova, Alexander E Ivliev, Birgitt Schüle, Birgit Schüle, Jeff Alexander, William Wallace, Glenda M Halliday and 5 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 42 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 6 pooled it
3.4field-weighted citation impact, top 8% 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

42 citing papers in PubMed, 6 syntheses or guidelines pooled it, 92 citations in OpenAlex.

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  12. Protein Translation in the Pathogenesis of Parkinson's Disease.International journal of molecular sciences · 2024
    Review
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4 · The record

Corrections and comments

  • Erratum issued
    Schüle, Birgit [corrected to Schüle, Birgitt]
5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Brigit E RileyElan Pharmaceuticals, South San Francisco, California, United States of America.
Shyra J GardaiElan Pharmaceuticals, South San Francisco, California, United States of America.
Dorothea Emig-AgiusThomson Reuters, Carlsbad, California, United States of America.
Marina BessarabovaThomson Reuters, Carlsbad, California, United States of America.
Alexander E IvlievThomson Reuters, Carlsbad, California, United States of America.
Birgitt Schüle
Birgit SchüleThe Parkinson's Institute, Sunnyvale, California, United States of America.
Jeff AlexanderElan Pharmaceuticals, South San Francisco, California, United States of America.
William WallaceElan Pharmaceuticals, South San Francisco, California, United States of America.
Glenda M HallidayNeuroscience Research Australia and the University of New South Wales, Sydney, N.S.W., Australia.
J William LangstonThe Parkinson's Institute, Sunnyvale, California, United States of America.
Scott BraxtonThomson Reuters, Carlsbad, California, United States of America.
Ted YednockElan Pharmaceuticals, South San Francisco, California, United States of America.
Thomas ShalerSRI International, Menlo Park, California, United States of America.
Jennifer A JohnstonElan Pharmaceuticals, South San Francisco, California, United States of America.
Thomson Reuters (United States) · USParkinson's Institute and Clinical Center · USSRI International · USUNSW Sydney · AU

Funding

ROLE OF PROGESTERONE RECEPTOR RATIO IN BREAST CANCERF32CA090073 · NCI · UNIVERSITY OF COLORADO DENVER · PI JACOBSEN, BRITTA M · 2001 to 2003
$127k
NCI NIH HHS F32 CA090073
6 · The paper itself

Abstract

Detailed analysis of disease-affected tissue provides insight into molecular mechanisms contributing to pathogenesis. Substantia nigra, striatum, and cortex are functionally connected with increasing degrees of alpha-synuclein pathology in Parkinson's disease. We undertook functional and causal pathway analysis of gene expression and proteomic alterations in these three regions, and the data revealed pathways that correlated with disease progression. In addition, microarray and RNAseq experiments revealed previously unidentified causal changes related to oligodendrocyte function and synaptic vesicle release, and these and other changes were reflected across all brain regions. Importantly, subsets of these changes were replicated in Parkinson's disease blood; suggesting peripheral tissue may provide important avenues for understanding and measuring disease status and progression. Proteomic assessment revealed alterations in mitochondria and vesicular transport proteins that preceded gene expression changes indicating defects in translation and/or protein turnover. Our combined approach of proteomics, RNAseq and microarray analyses provides a comprehensive view of the molecular changes that accompany functional loss and alpha-synuclein pathology in Parkinson's disease, and may be instrumental to understand, diagnose and follow Parkinson's disease progression.

Indexed as

alpha-SynucleinAnimalsBrainDisease ProgressionGene Expression RegulationHumansMicroarray AnalysisParkinson DiseaseProteinsProteomicsSequence Analysis, RNASignal Transductionalpha-SynucleinProteins

Identifiers

PMID25170892
PMCPMC4149353
OpenAlexW2067865628

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.