Evidence map›Paper›PMID 25501556›Full record

ArticlePloS one2014

Long leukocyte telomere length at diagnosis is a risk factor for dementia progression in idiopathic parkinsonism.

Sofie Degerman, Magdalena Domellöf, Mattias Landfors, Jan Linder, Mathias Lundin, Susann Haraldsson, Eva Elgh, Göran Roos, Lars Forsgren

Open 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. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Interplay Between 3D Chromatin Architecture and Gene Regulation at theInternational journal of molecular sciences · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Telomere Attrition in Neurodegenerative Disorders.Frontiers in cellular neuroscience · 2020
    Article
  17. Cellular Senescence in Neurodegenerative Diseases.Frontiers in cellular neuroscience · 2020
    Review
  18. Article
  19. Article
  20. Ageing, Cellular Senescence and Neurodegenerative Disease.International journal of molecular sciences · 2018
    Review
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

9 authors at 1 institution in 1 country.

Sofie DegermanDepartment of Medical Biosciences, Umeå University, Umeå, Sweden.
Magdalena DomellöfDepartment of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
Mattias LandforsDepartment of Medical Biosciences, Umeå University, Umeå, Sweden.
Jan LinderDepartment of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
Mathias LundinDepartment of Statistics, Umeå University, Umeå, Sweden.
Susann HaraldssonDepartment of Medical Biosciences, Umeå University, Umeå, Sweden.
Eva ElghDepartment of Community Medicine and Rehabilitation, Umeå University, Umeå, Sweden.
Göran RoosDepartment of Medical Biosciences, Umeå University, Umeå, Sweden.
Lars ForsgrenDepartment of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
Umeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomere length (TL) is regarded as a marker of cellular aging due to the gradual shortening by each cell division, but is influenced by a number of factors including oxidative stress and inflammation. Parkinson's disease and atypical forms of parkinsonism occur mainly in the elderly, with oxidative stress and inflammation in afflicted cells. In this study the relationship between blood TL and prognosis of 168 patients with idiopathic parkinsonism (136 Parkinson's disease [PD], 17 Progressive Supranuclear Palsy [PSP], and 15 Multiple System Atrophy [MSA]) and 30 controls was investigated. TL and motor and cognitive performance were assessed at baseline (diagnosis) and repeatedly up to three to five years follow up. No difference in TL between controls and patients was shown at baseline, nor any significant difference in TL stability or attrition during follow up. Interestingly, a significant relationship between TL at diagnosis and cognitive phenotype at follow up in PD and PSP patients was found, with longer mean TL at diagnosis in patients that developed dementia within three years.

Indexed as

AdultAgedAged, 80 and overDementiaFemaleHumansLeukocytesMaleMiddle AgedMultiple System AtrophyParkinson DiseasePrognosisSupranuclear Palsy, ProgressiveTelomere

Identifiers

PMID25501556
PMCPMC4264694
OpenAlexW2079744861

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.