Evidence map›Paper›PMID 42244277›Full record

ArticleAnnals of dermatology2026

Effects of Botulinum Toxin A on Rosacea-Like Inflammation in an LL-37-Induced Rosacea Mouse Model.

Daewon Yoon, Jung Ok Lee, You Na Jang, Kwang Ho Yoo, Beom Joon Kim, Sun Young Choi

Abstract read
In one paragraph

Article in Annals of dermatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Daewon Yoon *Department of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0009-0007-5454-0159
Jung Ok Lee *Department of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0048-5322
You Na JangDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0014-9783
Kwang Ho YooDepartment of Dermatology, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Gwangmyeong, Korea.ORCID https://orcid.org/0000-0002-0137-6849
Beom Joon KimDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2320-7621
Sun Young ChoiDepartment of Dermatology, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Gwangmyeong, Korea. sun02ya@naver.com.ORCID https://orcid.org/0000-0003-0248-7708

Funding

Amorepacific
6 · The paper itself

Abstract

backgroundRosacea is a chronic inflammatory disorder characterized by flushing, erythema, papules/pustules, and telangiectasia. Several clinical studies have investigated the efficacy of botulinum neurotoxin A (BoNT/A) in the treatment of rosacea, but its mechanism of action remains unclear.

objectiveThis study aims to examine the potential role of BoNT/A in a mouse model of rosacea-like skin lesions induced by the 37-amino acid C-terminal cathelicidin peptide (LL-37).

methodsMice were randomly divided into 4 groups: Control, LL-37, LL-37 + BoNT/A, and LL-37 + dexamethasone.

resultsBoNT/A treatment alleviated skin damage, reduced skin thickness, and decreased mast cell infiltration. Furthermore, BoNT/A improved redness score severity and redness area while enhancing skin barrier function by suppressing transepidermal water loss and increasing skin hydration. At the molecular level, BoNT/A decreased the mRNA levels of interleukin (IL)-6 and tumor necrosis factor-α, which are known as pro-inflammatory cytokines. It also downregulated the expression of pyrin domain-containing protein 3, caspase-1, and IL-1 beta in the LL-37-injected dorsal skin. Furthermore, BoNT/A prevented LL-37-mediated upregulation of neurovascular-associated factors, including CD31, transient receptor potential vanilloid 1, calcitonin-related polypeptide alpha, vascular endothelial growth factor, chymase 1, and tryptase alpha/beta 1.

conclusionThese results indicate that BoNT/A effectively alleviates inflammatory and vascular responses in a rosacea mouse model, highlighting its potential as a promising preventive approach for rosacea.

Indexed as

AngiogenesisBotulinum toxin AInflammasomesNeurogenic inflammationRosace

Identifiers

PMID42244277
PMCPMC13243716

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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.