Evidence map›Paper›PMID 28617319›Full record

ReviewInternational journal of molecular sciences2017

PDE4 Inhibition and Inflammatory Bowel Disease: A Novel Therapeutic Avenue.

Marco Spadaccini, Silvia D'Alessio, Laurent Peyrin-Biroulet, Silvio Danese

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
–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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
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  5. EngineeredActa pharmaceutica Sinica. B · 2025
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  18. Research progress of phosphodiesterase inhibitors in inflammatory bowel disease treatment.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2021
    Review
  19. Small Molecule Drugs in Inflammatory Bowel Diseases.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  20. 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

4 authors.

Marco SpadacciniLaboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center, Milan 20089, Italy. marco.spadaccini@humanitas.it.
Silvia D'AlessioLaboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center, Milan 20089, Italy. silvia.dalessio@humanitasresearch.it.
Laurent Peyrin-BirouletDepartment of Hepato-Gastroenterology and Inserm U954, University Hospital of Nancy, Lorraine University, Vandoeuvre-lès-Nancy 54500, France. peyrinbiroulet@gmail.com.
Silvio DaneseLaboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center, Milan 20089, Italy. silvio.danese@humanitas.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the last few decades, a better knowledge of the inflammatory pathways involved in the pathogenesis of Inflammatory Bowel Disease (IBD) has promoted biological therapy as an important tool to treat IBD patients. However, in spite of a wider spectrum of biological drugs, a significant proportion of patients is unaffected by or lose their response to these compounds, along with increased risks of infections and malignancies. For these reasons there is an urgent need to look for new pharmacological targets. The novel Phosphodiesterase 4 (PDE4) inhibitors have been recently introduced as new modulators of intracellular signals and gene transcription for the treatment of IBD.

aimTo discuss and describe the state of the art of this new class of compounds in the IBD field, with particular attention to apremilast.

methodsPublished articles selected from PubMed were comprehensively reviewed, with key words including apremilast, inflammatory disease, IBD, psoriasis, psoriatic arthritis, pathogenesis, therapies, and treatment.

resultsPDE4 inhibitors generate elevated intracellular levels of cyclic Adenosine Monophosphate (cAMP), that consequently down-regulate the release of pro-inflammatory cytokines in the mucosa of IBD patients. The newly developed apremilast is one of these drugs and has already been approved for the treatment of dermatologic/rheumatologic inflammatory conditions; studies in psoriasis and psoriatic arthritis have in fact demonstrated its clinical activity. However, no clinical trials have yet been published on the use of apremilast in IBD.

conclusionIn light of the similarity of pro-inflammatory signaling pathways across the gut, the skin, and joints, apremilast is likely supposed to show its efficacy also in IBD.

Indexed as

AnimalsCyclic Nucleotide Phosphodiesterases, Type 4Drug Evaluation, PreclinicalHumansInflammatory Bowel DiseasesMolecular Targeted TherapyPhosphodiesterase 4 InhibitorsThalidomideapremilastCyclic Nucleotide Phosphodiesterases, Type 4Phosphodiesterase 4 InhibitorsThalidomideapremilastInflammatory Bowel DiseasePDE4

Identifiers

PMID28617319
PMCPMC5486098

What OpenQuestion holds

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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.