Evidence map›Paper›PMID 34345187›Full record

ReviewJournal of experimental pharmacology2021

Experimental Pharmacological Management of Psoriasis.

Elena Campione, Terenzio Cosio, Monia Di Prete, Caterina Lanna, Annunziata Dattola, Luca Bianchi

Abstract readReview
In one paragraph

Review in Journal of experimental pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Review
  10. Review
  11. Article
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  13. Review
  14. Article
  15. Variants in PRKCE and KLC1, Potential Regulators of Type I Psoriasis.Clinical, cosmetic and investigational dermatology · 2022
    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

6 authors.

Elena CampioneDermatologic Unit, Department of Systems Medicine, University of Rome Tor Vergata, Rome, 00133, Italy.ORCID 0000-0001-7447-6798
Terenzio CosioDermatologic Unit, Department of Systems Medicine, University of Rome Tor Vergata, Rome, 00133, Italy.ORCID 0000-0003-4025-7882
Monia Di PreteAnatomic Pathology, University of Rome Tor Vergata, Rome, 00133, Italy.ORCID 0000-0002-3881-8540
Caterina LannaDermatologic Unit, Department of Systems Medicine, University of Rome Tor Vergata, Rome, 00133, Italy.ORCID 0000-0002-3485-6275
Annunziata DattolaDermatologic Unit, Department of Systems Medicine, University of Rome Tor Vergata, Rome, 00133, Italy.
Luca BianchiDermatologic Unit, Department of Systems Medicine, University of Rome Tor Vergata, Rome, 00133, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a chronic, relapsing, immune-mediated systemic disease. Its pathogenesis is complex and not fully understood yet. Genetic and epigenetic factors interact with molecular pathways involving TNF-α, IL-23/IL-17 axis, and peculiar cytokines, as IL-36 or phosphodiesterase 4. This review discusses the mechanisms involved in the development of the disease, as well as the therapeutic options proposed following the investigation of the inflammatory psoriatic pathways. We performed a comprehensive search using the words "psoriasis" and the newest molecules currently under investigation and approval. From these data, a new scenario in psoriasis is occurring to personalize the therapies - especially systemic ones and those using small molecules - and avoid topical and injectable drugs. We reported the newest therapeutic opportunities, including the inhibitors of Janus kinase/tyrosine kinase 2, phosphodiesterase-4 and IL-36 receptor. Today, more than 20 molecules are under investigation for the treatment of cutaneous psoriasis. Most of them are constituted by small molecules or biologic therapies. This underlines how psoriasis needs systemic therapies, due to its complex pathogenesis and multisystemic involvement.

Indexed as

IL-36 receptors inhibitorsjanus kinase inhibitorsphosphodiesterase 4 inhibitorspsoriasistyrosine kinase 2 inhibitors

Identifiers

PMID34345187
PMCPMC8323855

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.