Evidence map›Paper›PMID 17538633›Full record

ArticleGenes and immunity2007

The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases.

P L De Jager, D Franchimont, A Waliszewska, A Bitton, A Cohen, D Langelier, J Belaiche, S Vermeire, L Farwell, A Goris and 19 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
8.8field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 146 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Insight Into Polysaccharides FromFrontiers in immunology · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Glutamatergic Signaling Along The Microbiota-Gut-Brain Axis.International journal of molecular sciences · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Gut microbiota and IBD: causation or correlation?Nature reviews. Gastroenterology & hepatology · 2017
    Review
  15. Article
  16. Observational
  17. Article
  18. Review
  19. Article
  20. Association among genetic predisposition, gut microbiota, and host immune response in the etiopathogenesis of inflammatory bowel disease.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2014
    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

29 authors at 17 institutions in 3 countries.

P L De JagerDepartment of Neurology, Center for Neurologic Diseases, Brigham & Women's Hospital and Harvard Medical School, Boston, MA, USA.
D Franchimont
A Waliszewska
A Bitton
A Cohen
D Langelier
J Belaiche
S Vermeire
L Farwell
A Goris
C Libioulle
N Jani
T Dassopoulos
G P Bromfield
B Dubois
J H Cho
S R Brant
R H Duerr
H Yang
J I Rotter
M S Silverberg
A H Steinhart
M J Daly
D K Podolsky
E Louis
D A Hafler
J D Rioux
Quebec IBD Genetics Consortium
NIDDK IBD Genetics Consortium
University of Liège · BECedars-Sinai Medical Center · USHarvard University · USJohns Hopkins University · USKU Leuven · BEMassachusetts Institute of Technology · USUniversity of Pittsburgh · USUniversity of Toronto · CABrigham and Women's Hospital · USBroad Institute · USCentre Hospitalier Universitaire de Sherbrooke · CAJewish General Hospital · CAMassachusetts General Hospital · USMcGill University Health Centre · CAMontreal General Hospital · CAUniversity of Chicago · USYale University · US

Funding

NIDDK IBD Genetics Consortium Genetic Research CenterU01DK062420 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DUERR, RICHARD H · 2002 to 2021
$7.8M
NIDDK NIH HHS U01 DK062420
6 · The paper itself

Abstract

The intestinal flora has long been thought to play a role either in initiating or in exacerbating the inflammatory bowel diseases (IBD). Host defenses, such as those mediated by the Toll-like receptors (TLR), are critical to the host/pathogen interaction and have been implicated in IBD pathophysiology. To explore the association of genetic variation in TLR pathways with susceptibility to IBD, we performed a replication study and pooled analyses of the putative IBD risk alleles in NFKB1 and TLR4, and we performed a haplotype-based screen for association to IBD in the TLR genes and a selection of their adaptor and signaling molecules. Our genotyping of 1539 cases of IBD and pooled analysis of 4805 cases of IBD validates the published association of a TLR4 allele with risk of IBD (odds ratio (OR): 1.30, 95% confidence interval (CI): 1.15-1.48; P=0.00017) and Crohn's disease (OR: 1.33, 95% CI: 1.16-1.54; P=0.000035) but not ulcerative colitis. We also describe novel suggestive evidence that TIRAP (OR: 1.16, 95% CI: 1.04-1.30; P=0.007) has a modest effect on risk of IBD. Our analysis, therefore, offers additional evidence that the TLR4 pathway - in this case, TLR4 and its signaling molecule TIRAP - plays a role in susceptibility to IBD.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideFemaleGene FrequencyGenotypeHaplotypesHumansInflammatory Bowel DiseasesLongitudinal StudiesMaleMembrane GlycoproteinsReceptors, Interleukin-1Signal TransductionToll-Like Receptor 4Toll-Like ReceptorsMembrane GlycoproteinsReceptors, Interleukin-1TIRAP protein, humanTLR4 protein, humanToll-Like Receptor 4Toll-Like Receptors

Identifiers

PMID17538633
OpenAlexW2140541855

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.