Evidence map›Paper›PMID 18849290›Full record

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

Genetic susceptibility, evolution and the kuru epidemic.

Simon Mead, Jerome Whitfield, Mark Poulter, Paresh Shah, James Uphill, Jonathan Beck, Tracy Campbell, Huda Al-Dujaily, Holger Hummerich, Michael P Alpers and 1 more

Open access · hybridAbstract read
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 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 29% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Genetic aspects of human prion diseases.Frontiers in neurology · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. THE EXPOSOME IN HUMAN EVOLUTION: FROM DUST TO DIESEL.The Quarterly review of biology · 2019
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Epidemiological mechanisms of genetic resistance to kuru.Journal of the Royal Society, Interface · 2013
    Article
  17. Review
  18. Kuru: genes, cannibals and neuropathology.Journal of neuropathology and experimental neurology · 2012
    Review
  19. Review
  20. Review. Lessons of kuru research: background to recent studies with some personal reflections.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2008
    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

11 authors at 4 institutions in 3 countries.

Simon MeadDepartment of Neurodegenerative Disease, MRC Prion Unit, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Jerome Whitfield
Mark Poulter
Paresh Shah
James Uphill
Jonathan Beck
Tracy Campbell
Huda Al-Dujaily
Holger Hummerich
Michael P Alpers
John Collinge
University College London · GBNational Hospital for Neurology and Neurosurgery · GBCurtin University · AUMRC Prion Unit · GB

Funding

Medical Research Council MC_U123160651Medical Research Council MC_U123160657Medical Research Council MC_U123192748
6 · The paper itself

Abstract

The acquired prion disease kuru was restricted to the Fore and neighbouring linguistic groups of the Papua New Guinea highlands and largely affected children and adult women. Oral history documents the onset of the epidemic in the early twentieth century, followed by a peak in the mid-twentieth century and subsequently a well-documented decline in frequency. In the context of these strong associations (gender, region and time), we have considered the genetic factors associated with susceptibility and resistance to kuru. Heterozygosity at codon 129 of the human prion protein gene (PRNP) is known to confer relative resistance to both sporadic and acquired prion diseases. In kuru, heterozygosity is associated with older patients and longer incubation times. Elderly survivors of the kuru epidemic, who had multiple exposures at mortuary feasts, are predominantly PRNP codon 129 heterozygotes and this group show marked Hardy-Weinberg disequilibrium. The deviation from Hardy-Weinberg equilibrium is most marked in elderly women, but is also significant in a slightly younger cohort of men, consistent with their exposure to kuru as boys. Young Fore and the elderly from populations with no history of kuru show Hardy-Weinberg equilibrium. An increasing cline in 129V allele frequency centres on the kuru region, consistent with the effect of selection in elevating the frequency of resistant genotypes in the exposed population. The genetic data are thus strikingly correlated with exposure. Considering the strong coding sequence conservation of primate prion protein genes, the number of global coding polymorphisms in man is surprising. By intronic resequencing in a European population, we have shown that haplotype diversity at PRNP comprises two major and divergent clades associated with 129M and 129V. Kuru may have imposed the strongest episode of recent human balancing selection, which may not have been an isolated episode in human history.

Indexed as

Genetic VariationEthnicityFemaleGene FrequencyGenetic Predisposition to DiseaseHaplotypesHeterozygoteHumansKuruMalePapua New GuineaPrion ProteinsPrionsSelection, GeneticPrion ProteinsPrionsPRNP protein, human

Identifiers

PMID18849290
PMCPMC2576515
OpenAlexW2163829697

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.