Evidence map›Paper›PMID 18849292›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2008

Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease.

Sebastian Brandner, Jerome Whitfield, Ken Boone, Anderson Puwa, Catherine O'Malley, Jacqueline M Linehan, Susan Joiner, Francesco Scaravilli, Ian Calder, Michael P Alpers and 2 more

Open access · greenAbstract readCase ReportsComparative Study
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 72 citations in OpenAlex.

  1. Prion diseases: Lessons from historical outbreaks and potential emerging ones.Protein science : a publication of the Protein Society · 2025
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Prion Strains and Transmission Barrier Phenomena.Pathogens (Basel, Switzerland) · 2018
    Review
  8. Sporadic and Infectious Human Prion Diseases.Cold Spring Harbor perspectives in medicine · 2017
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Prion disease: a tale of folds and strains.Brain pathology (Zurich, Switzerland) · 2013
    Review
  15. Kuru: genes, cannibals and neuropathology.Journal of neuropathology and experimental neurology · 2012
    Review
  16. An overview of human prion diseases.Virology journal · 2011
    Review
  17. Review
  18. Molecular pathology of human prion disease.Acta neuropathologica · 2011
    Review
  19. Review
  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

12 authors at 4 institutions in 3 countries.

Sebastian BrandnerDepartment of Neurodegenerative Disease, MRC Prion Unit, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Jerome Whitfield
Ken Boone
Anderson Puwa
Catherine O'Malley
Jacqueline M Linehan
Susan Joiner
Francesco Scaravilli
Ian Calder
Michael P Alpers
Jonathan D F Wadsworth
John Collinge
National Hospital for Neurology and Neurosurgery · GBUniversity College London · GBMRC Prion Unit · GBPapua New Guinea Institute of Medical Research · PG

Funding

Medical Research Council MC_U123160655Medical Research Council MC_U123160657Medical Research Council MC_U123192748
6 · The paper itself

Abstract

While the neuropathology of kuru is well defined, there are few data concerning the distribution of disease-related prion protein in peripheral tissues. Here we report the investigation of brain and peripheral tissues from a kuru patient who died in 2003. Neuropathological findings were compared with those seen in classical (sporadic and iatrogenic) Creutzfeldt-Jakob disease (CJD) and variant CJD (vCJD). The neuropathological findings of the kuru patient showed all the stereotypical changes that define kuru, with the occurrence of prominent PrP plaques throughout the brain. Lymphoreticular tissue showed no evidence of prion colonization, suggesting that the peripheral pathogenesis of kuru is similar to that seen in classical CJD rather than vCJD. These findings now strongly suggest that the characteristic peripheral pathogenesis of vCJD is determined by prion strain type alone rather than route of infection.

Indexed as

Disease ProgressionHumansImmunoblottingImmunohistochemistryKuruMaleMiddle AgedNervous SystemPrionsPrions

Identifiers

PMID18849292
PMCPMC2581659
OpenAlexW2107167553

What OpenQuestion holds

Textmetadata
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.