Evidence map›Paper›PMID 16405727›Full record

ArticleBMC infectious diseases2006

Comparative evidence for a link between Peyer's patch development and susceptibility to transmissible spongiform encephalopathies.

Suzanne G St Rose, Nora Hunter, Louise Matthews, James D Foster, Margo E Chase-Topping, Loeske E B Kruuk, Darren J Shaw, Susan M Rhind, Robert G Will, Mark E J Woolhouse

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC infectious diseases, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.0field-weighted citation impact, top 9% 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, 55 citations in OpenAlex.

  1. BSE risk posed by ruminant collagen and gelatine derived from bones.EFSA journal. European Food Safety Authority · 2024
    Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. How do PrPPathogens (Basel, Switzerland) · 2017
    Review
  7. Article
  8. Article
  9. Sporadic and Infectious Human Prion Diseases.Cold Spring Harbor perspectives in medicine · 2017
    Review
  10. Article
  11. The molecular epidemiology of variant CJD.International journal of molecular epidemiology and genetics · 2011
    Article
  12. Article
  13. Article
  14. Article
  15. Transmission and detection of prions in feces.The Journal of infectious diseases · 2008
    Article
  16. Evidence of scrapie transmission via milk.BMC veterinary research · 2008
    Article
  17. Article
  18. Article
  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

10 authors at 5 institutions in 1 country.

Suzanne G St RoseCentre for Infectious Diseases, University of Edinburgh, King's Buildings, Edinburgh EH9 3JF, UK. s0231156@sms.ed.ac.uk
Nora Hunter
Louise Matthews
James D Foster
Margo E Chase-Topping
Loeske E B Kruuk
Darren J Shaw
Susan M Rhind
Robert G Will
Mark E J Woolhouse
University of Edinburgh · GBThe Pirbright Institute · GBRoslin Institute · GBUniversity of Glasgow · GBWestern General Hospital · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundEpidemiological analyses indicate that the age distribution of natural cases of transmissible spongiform encephalopathies (TSEs) reflect age-related risk of infection, however, the underlying mechanisms remain poorly understood. Using a comparative approach, we tested the hypothesis that, there is a significant correlation between risk of infection for scrapie, bovine spongiform encephalopathy (BSE) and variant CJD (vCJD), and the development of lymphoid tissue in the gut.

methodsUsing anatomical data and estimates of risk of infection in mathematical models (which included results from previously published studies) for sheep, cattle and humans, we calculated the Spearman's rank correlation coefficient, rs, between available measures of Peyer's patch (PP) development and the estimated risk of infection for an individual of the corresponding age.

resultsThere was a significant correlation between the measures of PP development and the estimated risk of TSE infection; the two age-related distributions peaked in the same age groups. This result was obtained for each of the three host species: for sheep, surface area of ileal PP tissue vs risk of infection, rs = 0.913 (n = 19, P < 0.001), and lymphoid follicle density vs risk of infection, rs = 0.933 (n = 19, P < 0.001); for cattle, weight of PP tissue vs risk of infection, rs = 0.693 (n = 94, P < 0.001); and for humans, number of PPs vs risk of infection, rs = 0.384 (n = 46, P = 0.008). In addition, when changes in exposure associated with BSE-contaminated meat were accounted for, the two age-related patterns for humans remained concordant: rs = 0.360 (n = 46, P = 0.014).

conclusionOur findings suggest that, for sheep, cattle and humans alike there is an association between PP development (or a correlate of PP development) and susceptibility to natural TSE infection. This association may explain changes in susceptibility with host age, and differences in the age-susceptibility relationship between host species.

Indexed as

Age DistributionAnimalsCattleCattle DiseasesDisease SusceptibilityHumansPeyer's PatchesPrion DiseasesRisk FactorsSheepSheep DiseasesSpecies Specificity

Identifiers

PMID16405727
PMCPMC1361786
OpenAlexW2121527997

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.