Evidence map›Paper›PMID 26640330›Full record

ReviewWorld journal of gastroenterology2015

Update on pathogenesis and predictors of response of therapeutic strategies used in inflammatory bowel disease.

Emilio G Quetglas, Zlatan Mujagic, Simone Wigge, Daniel Keszthelyi, Sebastian Wachten, Ad Masclee, Walter Reinisch

Abstract readReview
In one paragraph

Review in World journal of gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. [Anti-inflammatory effect of interleukin-35 in mice with colitis and its mechanism].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2018
    Article
  6. Article
  7. Article
  8. Review
  9. Current understanding concerning intestinal stem cells.World journal of gastroenterology · 2016
    Review
  10. Review
  11. Article
  12. 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

7 authors.

Emilio G QuetglasEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.
Zlatan MujagicEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.
Simone WiggeEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.
Daniel KeszthelyiEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.
Sebastian WachtenEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.
Ad MascleeEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.
Walter ReinischEmilio G Quetglas, Project Strategy and Science, Grünenthal GmbH, 52078 Aachen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The search for biomarkers that characterize specific aspects of inflammatory bowel disease (IBD), has received substantial interest in the past years and is moving forward rapidly with the help of modern technologies. Nevertheless, there is a direct demand to identify adequate biomarkers for predicting and evaluating therapeutic response to different therapies. In this subset, pharmacogenetics deserves more attention as part of the endeavor to provide personalized medicine. The ultimate goal in this area is the adjustment of medication for a patient's specific genetic background and thereby to improve drug efficacy and safety rates. The aim of the following review is to utilize the latest knowledge on immunopathogenesis of IBD and update the findings on the field of Immunology and Genetics, to evaluate the response to the different therapies. In the present article, more than 400 publications were reviewed but finally 287 included based on design, reproducibility (or expectancy to be reproducible and translationable into humans) or already measured in humans. A few tests have shown clinical applicability. Other, i.e., genetic associations for the different therapies in IBD have not yet shown consistent or robust results. In the close future it is anticipated that this, cellular and genetic material, as well as the determination of biomarkers will be implemented in an integrated molecular diagnostic and prognostic approach to manage IBD patients.

Indexed as

AnimalsAnti-Inflammatory AgentsBiotransformationDiagnostic ImagingDrug MonitoringGastrointestinal AgentsGenetic MarkersGenetic Predisposition to DiseaseHumansInflammation MediatorsInflammatory Bowel DiseasesMolecular Diagnostic TechniquesPhenotypePredictive Value of TestsTreatment OutcomeAnti-Inflammatory AgentsGastrointestinal AgentsGenetic MarkersInflammation MediatorsBiomarkersMode of actionMucosal immunologyPharmacologyTherapeutic drug monitoring

Identifiers

PMID26640330
PMCPMC4658608

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.