Evidence map›Paper›PMID 28725688›Full record

ArticleNPJ Parkinson's disease2015

Delaying aging is neuroprotective in Parkinson's disease: a genetic analysis in

Jason F Cooper, Dylan J Dues, Katie K Spielbauer, Emily Machiela, Megan M Senchuk, Jeremy M Van Raamsdonk

Open access · goldAbstract read
In one paragraph

Article in NPJ Parkinson's disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

59 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Frontiers in molecular biosciences · 2025
    Article
  7. Article
  8. Regulation of TIR-1/SARM-1 by miR-71 Protects Dopaminergic Neurons in aInternational journal of molecular sciences · 2024
    Article
  9. 2-Butoxytetrahydrofuran, Isolated fromACS chemical neuroscience · 2024
    Article
  10. Review
  11. Article
  12. Anti-Parkinson Effects ofMarine drugs · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Jason F CooperCenter for Neurodegenerative Science, Laboratory of Aging and Neurodegenerative Disease, Van Andel Research Institute, Grand Rapids, MI, USA.
Dylan J DuesCenter for Neurodegenerative Science, Laboratory of Aging and Neurodegenerative Disease, Van Andel Research Institute, Grand Rapids, MI, USA.
Katie K SpielbauerCenter for Neurodegenerative Science, Laboratory of Aging and Neurodegenerative Disease, Van Andel Research Institute, Grand Rapids, MI, USA.
Emily MachielaCenter for Neurodegenerative Science, Laboratory of Aging and Neurodegenerative Disease, Van Andel Research Institute, Grand Rapids, MI, USA.
Megan M SenchukCenter for Neurodegenerative Science, Laboratory of Aging and Neurodegenerative Disease, Van Andel Research Institute, Grand Rapids, MI, USA.
Jeremy M Van RaamsdonkCenter for Neurodegenerative Science, Laboratory of Aging and Neurodegenerative Disease, Van Andel Research Institute, Grand Rapids, MI, USA.
Van Andel Institute · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

Aging is the greatest risk factor for the development of Parkinson's disease (PD). However, the role of aging in the pathogenesis of PD is not known and it is currently uncertain why the symptoms take many decades to develop when inherited mutations that cause the disease can be present from birth. We hypothesize that there are specific changes that take place during the aging process that make cells susceptible to disease-causing mutations that are well-tolerated at younger ages. If so, then interventions that increase lifespan should be beneficial in the treatment of PD. To test this hypothesis, we used the powerful genetics of

Identifiers

PMID28725688
PMCPMC5516561
OpenAlexW2592662044

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.