Evidence map›Paper›PMID 24108702›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2013

Specific splice variants are associated with Parkinson's disease.

Jose A Santiago, Clemens R Scherzer, Harvard Biomarker Study, Judith A Potashkin

Open access · greenAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. The Potential ofGenes · 2023
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Reply to Toker and Pavlidis: Blood biomarkers for Parkinson's disease.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  11. Network-based metaanalysis identifies HNF4A and PTBP1 as longitudinally dynamic biomarkers for Parkinson's disease.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  12. Observational
  13. Review
  14. Article
  15. 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

4 authors at 2 institutions in 1 country.

Jose A SantiagoDepartment of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois, USA.
Clemens R Scherzer
Harvard Biomarker Study
Judith A Potashkin
Brigham and Women's Hospital · USRosalind Franklin University of Medicine and Science · US

Funding

Creatine Safety, Tolerability, and Efficacy in Huntington's Disease: CREST-EU01AT000613 · NCCIH · MASSACHUSETTS GENERAL HOSPITAL · PI HERSCH, STEVEN M · 2007 to 2015
$12.9M
Neuroimaging Biomarkers for disease-modyfying therapies in Hintington's diseaseP01NS058793 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI HERSCH, STEVEN M · 2008 to 2012
$6.6M
Biomarkers for early intervention in Parkinson diseaseU01NS082157 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2012 to 2016
$2.5M
Genome-wide analysis of tau neurotoxicityR01AG044113 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI FEANY, MEL B · 2012 to 2016
$2.0M
Risk Marker for Parkinson's Disease: Enabling Novel TherapiesR01NS064155 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2008 to 2011
$1.7M
A Next Generation of Biomarkers for Incipient Huntington DiseaseU01NS082080 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2013 to 2015
$1.5M
NCCIH NIH HHS U01 AT000613NIA NIH HHS R01 AG044113NINDS NIH HHS P01 NS058793NINDS NIH HHS R01 NS064155NINDS NIH HHS U01 NS082080NINDS NIH HHS U01 NS082157
6 · The paper itself

Abstract

backgroundDiagnosis of Parkinson's disease (PD) currently relies on assessment of motor symptoms. Recently, sensitive, specific, and readily available splice variant-specific biomarkers were identified in peripheral blood from participants in the Diagnostic and Prognostic Biomarkers in Parkinson Disease study.

methodsHere we test for an association between candidate splice variant biomarkers and PD in blood of an independent population of cases and controls nested in the Harvard NeuroDiscovery Center Biomarker Study.

resultsExpression of 7 out of 13 candidate biomarkers was dysregulated in whole cellular blood of patients with PD.

conclusionsThese results support the view that differential expression of a subset of splice-variant markers in blood is associated with PD. Further evaluation in untreated, de novo patients and at-risk subjects is warranted.

Indexed as

AgedBiomarkersFemaleHumansMaleMiddle AgedParkinson DiseaseProtein IsoformsBiomarkersProtein Isoformsbiomarkergene expressionneurodegenerationParkinson's diseasesplicing

Identifiers

PMID24108702
PMCPMC3812386
OpenAlexW1917383504

What OpenQuestion holds

Textmetadata
LicenceTDM
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.