Evidence map›Paper›PMID 18377803›Full record

ReviewCurrent gastroenterology reports2007

Microbial host interactions in IBD: implications for pathogenesis and therapy.

R Balfour Sartor, Marcus Muehlbauer

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Current gastroenterology reports, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02516384 (Fecal Microbiota Transplantation), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.0field-weighted citation impact, top 5% 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.

NCT02516384 phase1completednot on this mapstarted 2016, after this paper: background citation

Fecal Microbiota Transplantation (FMT) in the Management of Ulcerative Colitis (UC)

TypeinterventionalSponsorWeill Medical College of Cornell UniversityRan2016 to 2017Enrolled20ConditionsUlcerative ColitisArmsFecal Microbiota Transplantation
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. BioMed research international · 2022
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Clinical microbiology reviews · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Crohn's disease: a clinical update.Therapeutic advances in gastroenterology · 2015
    Review
  18. Article
  19. Article
  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

2 authors at 1 institution in 1 country.

R Balfour SartorDepartment of Medicine, Center for Gastrointestinal Biology and Disease, University of North Carolina at Chapel Hill, CB #7032, Room 7309, Medical Biomolecular Research Building, Chapel Hill, NC 27599, USA. rbs@med.unc.edu
Marcus Muehlbauer
University of North Carolina at Chapel Hill · US

Funding

PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Temitope O. Keku · 1985 to 2026
$30.5M
Colitis Induced by immune responses to luminal bacteria-mouseR01DK053347 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SARTOR, RYAN B · 1998 to 2012
$4.6M
MECHANISMS OF COLITIS INDUCED BY DEFINED BACTERIAL FLORAR01DK040249 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SARTOR, RYAN B · 1989 to 2011
$3.0M
NIDDK NIH HHS P30 DK34987NIDDK NIH HHS R01 DK40249NIDDK NIH HHS R01 DK53347
6 · The paper itself

Abstract

Crohn's disease (CD), ulcerative colitis (UC), and pouchitis appear to be caused by pathogenic T-cell responses to discrete antigens from the complex luminal microbiota, with susceptibility conferred by genetic polymorphisms that regulate bacterial killing, mucosal barrier function, or immune responses. Environmental triggers initiate or reactivate inflammation and modulate genetic susceptibility. New pathogenesis concepts include defective bacterial killing by innate immune cells in CD, colonization of the ileum in CD with functionally abnormal Escherichia coli that adhere to and invade epithelial cells and resist bacterial killing, and alterations in enteric microbiota composition in CD, UC, and pouchitis detected by molecular probes. The considerable therapeutic potential of manipulating the enteric microbiota in inflammatory bowel disease patients has not been realized, probably due to failure to recognize heterogenic disease mechanisms that require individualized use of antibiotics, probiotics, prebiotics, combination therapies, and genetically engineered bacteria to restore mucosal homeostasis.

Indexed as

AnimalsAnti-Infective AgentsBacterial Outer Membrane ProteinsColitis, UlcerativeCrohn DiseaseEpithelial CellsEscherichia coliGastric MucosaGenetic EngineeringHomeostasisHost-Pathogen InteractionsHumansInflammationInflammatory Bowel DiseasesPhagocytosisProbioticsAnti-Infective AgentsBacterial Outer Membrane ProteinsRifamycinsRifaximinTLR protein, bacteria

Identifiers

PMID18377803
OpenAlexW2080401272

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.