Evidence map›Paper›PMID 36154894›Full record

ReviewRedox report : communications in free radical research2022

Damage-associated molecular patterns in vitiligo: igniter fuse from oxidative stress to melanocyte loss.

Jingying Wang, Yinghao Pan, Guangmin Wei, Hanxiao Mao, Rulan Liu, Yuanmin He

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Redox report : communications in free radical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05869942 (Histological and Histochemical Study of Vitiligo Pathogenesis in Sohag University Hospital Patients), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 9% 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.

NCT05869942 naunknown statusnot on this mapstarted 2023, after this paper: background citation

Histological and Histochemical Study of Vitiligo Pathogenesis in Sohag University Hospital Patients

TypeinterventionalSponsorSohag UniversityRan2023 to 2024Enrolled60ConditionsVitiligoArmsLight microscopic studies, Immunohistochemical studies
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Identification of active compounds inFrontiers in pharmacology · 2024
    Article
  13. TanshinoneIIA inhibits melanocyte pyroptosis by regulating the ROS/NLRP3 signaling axis.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023
    Article
  14. Etiopathogenesis and Emerging Methods for Treatment of Vitiligo.International journal of molecular sciences · 2023
    Review
  15. 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.

Jingying WangDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Yinghao PanDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Guangmin WeiDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Hanxiao MaoDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Rulan LiuDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Yuanmin HeDepartment of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Affiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe pathogenesis of vitiligo remains unclear. In this review, we comprehensively describe the role of damage associated molecular patterns (DAMPs) during vitiligo pathogenesis.

methodsPublished papers on vitiligo, oxidative stress and DAMPs were collected and reviewed via database searching on PubMed, MEDLINE and Embase, etc.

resultsOxidative stress may be an important inducer of vitiligo. At high oxidative stress levels, damage-associated molecular patterns (DAMPs) are released from keratinocytes or melanocytes in the skin and induce downstream immune responses during vitiligo. Treatment regimens targeting DAMPs can effectively improve disease severity. DISCUSSION: DAMPs play key roles in initiating host defenses against danger signals, deteriorating the condition of vitiligo. DAMP levels in serum and skin may be used as biomarkers to indicate vitiligo activity and prognosis. Targeted therapies, incorporating HMGB1, Hsp70, and IL-15 could significantly improve disease etiology. Thus, novel strategies could be identified for vitiligo treatment by targeting DAMPs.

Indexed as

MelanocytesOxidative StressVitiligoBiomarkersHMGB1 ProteinHSP70 Heat-Shock ProteinsHumansInterleukin-15BiomarkersHMGB1 ProteinHSP70 Heat-Shock ProteinsInterleukin-15Adenosine triphosphate (ATP)Antimicrobial peptides (AMPs)damage-associated molecular patternsHeat shock protein 70 (Hsp70)High mobility group box 1 (HMGB1)Interleukinoxidative stresspathogenesisS100BVitiligo

Identifiers

PMID36154894
PMCPMC9518600
OpenAlexW4297064878

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.