Evidence map›Paper›PMID 35456955›Full record

ReviewInternational journal of molecular sciences2022

Opioidergic Signaling-A Neglected, Yet Potentially Important Player in Atopic Dermatitis.

Dorottya Ádám, József Arany, Kinga Fanni Tóth, Balázs István Tóth, Attila Gábor Szöllősi, Attila Oláh

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Frontiers in molecular neuroscience · 2022
    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

6 authors at 1 institution in 1 country.

Dorottya ÁdámDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0002-3543-4146
József AranyDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Kinga Fanni TóthDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0002-5184-8082
Balázs István TóthDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0002-4103-4333
Attila Gábor SzöllősiDepartment of Immunology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0001-6046-8236
Attila OláhDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0003-4122-5639
University of Debrecen · HU

Funding

Hungarian Academy of Sciences János Bolyai Research ScholarshipMinistry for Innovation and Technology ÚNKP-21-5-DE-465Ministry for Innovation and Technology ÚNKP-21-5-DE-491National Research, Development and Innovation Office 134235National Research, Development and Innovation Office 134725National Research, Development and Innovation Office 134993National Research, Development and Innovation Office EFOP-3.6.3-VEKOP-16-2017-00009National Research, Development and Innovation Office GINOP-2.3.2-15-2016-00026
6 · The paper itself

Abstract

Atopic dermatitis (AD) is one of the most common skin diseases, the prevalence of which is especially high among children. Although our understanding about its pathogenesis has substantially grown in recent years, and hence, several novel therapeutic targets have been successfully exploited in the management of the disease, we still lack curative treatments for it. Thus, there is an unmet societal demand to identify further details of its pathogenesis to thereby pave the way for novel therapeutic approaches with favorable side effect profiles. It is commonly accepted that dysfunction of the complex cutaneous barrier plays a central role in the development of AD; therefore, the signaling pathways involved in the regulation of this quite complex process are likely to be involved in the pathogenesis of the disease and can provide novel, promising, yet unexplored therapeutic targets. Thus, in the current review, we aim to summarize the available potentially AD-relevant data regarding one such signaling pathway, namely cutaneous opioidergic signaling.

Indexed as

Dermatitis, AtopicReceptors, OpioidAdministration, CutaneousChildHumansSignal TransductionSkinReceptors, Opioidatopic dermatitis (AD)cutaneous barrierinflammationitchkeratinocytemast cellnociceptin/orphanin FQ (NOP) receptoropioidskinδ-opioid receptor (DOR)κ-opioid receptor (KOR)µ-opioid receptor (MOR)

Identifiers

PMID35456955
PMCPMC9027603
OpenAlexW4224225705

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.