Evidence map›Paper›PMID 37212867›Full record

ReviewInflammation research : official journal of the European Histamine Research Society ... [et al.]2023

New small molecules in dermatology: for the autoimmunity, inflammation and beyond.

Paulo Ricardo Criado, Daniel Lorenzini, Hélio Amante Miot, Roberto Bueno-Filho, Francisca Regina Oliveira Carneiro, Mayra Ianhez

Open access · bronzeAbstract readReview
In one paragraph

Review in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Chronic pruritus: a narrative review.Anais brasileiros de dermatologia
    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 6 institutions in 1 country.

Paulo Ricardo CriadoFaculdade de Medicina Do ABC, Post-Graduation Program, Full Researcher, Santo André, Rua Carneiro Leão 33, Vila Scarpelli, Santo André, São Paulo, Brazil. prcriado@uol.com.br.ORCID http://orcid.org/0000-0001-9785-6099
Daniel LorenziniSanta Casa de Misericórida de Porto Alegre, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-6850-5799
Hélio Amante MiotUniversidade Estadual Paulista Júlio de Mesquita Filho (UNESP), Botucatu, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-2596-9294
Roberto Bueno-FilhoRibeirão Preto Medical School-University of São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0003-2871-0306
Francisca Regina Oliveira CarneiroUniversidade Do Estado Do Pará, UEPA-Belém, Belém, Brazil.ORCID http://orcid.org/0000-0001-6735-4004
Mayra IanhezUniversidade Federal de Goiás (UFG) E Hospital de Doenças Tropicais (HDT-GO), Goiânia, Goiás, Brazil.ORCID http://orcid.org/0000-0003-3604-3128
Faculdade de Medicina do ABC · BRSanta Casa de Misericórdia de Marília · BRUniversidade de Ribeirão Preto · BRUniversidade do Estado do Pará · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal de Goiás · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE AND

designThe discovery of new inflammatory pathways and the mechanism of action of inflammatory, autoimmune, genetic, and neoplastic diseases led to the development of immunologically driven drugs. We aimed to perform a narrative review regarding the rising of a new class of drugs capable of blocking important and specific intracellular signals in the maintenance of these pathologies: the small molecules. MATERIALS/

methodsA total of 114 scientific papers were enrolled in this narrative review.

resultsWe describe in detail the families of protein kinases-Janus Kinase (JAK), Src kinase, Syk tyrosine kinase, Mitogen-Activated Protein Kinase (MAPK), and Bruton Tyrosine Kinase (BTK)-their physiologic function and new drugs that block these pathways of intracellular signaling. We also detail the involved cytokines and the main metabolic and clinical implications of these new medications in the field of dermatology.

conclusionsDespite having lower specificity compared to specific immunobiological therapies, these new drugs are effective in a wide variety of dermatological diseases, especially diseases that had few therapeutic options, such as psoriasis, psoriatic arthritis, atopic dermatitis, alopecia areata, and vitiligo.

Indexed as

DermatologyPsoriasisVitiligoAutoimmunityHumansInflammationJanus KinasesJanus KinasesAtopicDermatitisJanus kinasesMitogen-activated protein kinase kinasesSrc-family kinasesSyk Kinase

Identifiers

PMID37212867
PMCPMC10201519
OpenAlexW4377220436

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.