Evidence map›Paper›PMID 35007355›Full record

ArticleExperimental dermatology2022

Gene expression profiling suggests severe, extensive central centrifugal cicatricial alopecia may be both clinically and biologically distinct from limited disease subtypes.

Taylor A Jamerson, C Conover Talbot, Yemisi Dina, Shawn G Kwatra, Luis A Garza, Crystal Aguh

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Experimental dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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.

NCT06946550 narecruitingnot on this mapstarted 2025, after this paper: background citation

1470 nm Non-Ablative Laser for the Treatment of Scarring Alopecia: A Clinical and Mechanistic Study

TypeinterventionalSponsorMontefiore Medical CenterRan2025 to 2027Enrolled5ConditionsScarring AlopeciaArms1470nm non-ablative fractional laser
NCT07734870 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Tirzepatide for Treatment of CCCA

TypeinterventionalSponsorJohns Hopkins UniversityRan2026 to 2028Enrolled20ConditionsCentral Centrifugal Cicatricial Alopecia (CCCA)ArmsTirzepatide
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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 at 2 institutions in 1 country.

Taylor A JamersonUniversity of Michigan Medical School, Ann Arbor, Michigan, USA.
C Conover TalbotJohns Hopkins Medical Institute Single Cell & Transcriptomics Core, Baltimore, Maryland, USA.
Yemisi DinaDepartment of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Shawn G KwatraDepartment of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Luis A GarzaDepartment of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-6547-9695
Crystal AguhDepartment of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-3590-9682
Johns Hopkins University · USUniversity of Michigan · US

Funding

Retinoic acid synthesis induced by noncoding dsRNA controls RegenerationR01AR074846 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI GARZA, LUIS ANDRES · 2019 to 2023
$2.3M
Injection of autologous volar fibroblasts to the stump site to allow pressure adaptation and enhanced prosthetic use in amputeesUG3AR079376 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI GARZA, LUIS ANDRES · 2021 to 2021
$532k
NIAMS NIH HHS L30 AR074129NIAMS NIH HHS R01 AR074846NIAMS NIH HHS UG3 AR079376
6 · The paper itself

Abstract

The natural history of central centrifugal cicatricial alopecia (CCCA) is widely variable. Some patients experience rapid progression to extensive, end-stage disease while others never approach extensive involvement over decades, suggesting heterogeneity in CCCA disease phenotype. To better characterize clinically severe disease in CCCA, tissue samples were obtained from the peripheral, hair-bearing lesional scalp of women with clinically focal, limited and extensive CCCA disease involvement. A microarray analysis was conducted to identify differential expression of genes previously identified to be preferentially expressed in the lesional scalp vs. non-lesional scalp of CCCA patients. Clinically extensive, severe CCCA was characterized by increased expression of MMP9, SFRP4 and MSR1 when directly compared with focal and limited disease. These biomarkers correspond to dysregulated pathways of fibrosis, Wnt signalling and macrophage-mediated inflammatory processes respectively. These findings hold significance for both possible targets for future study of prognostic markers of disease severity and new potential therapeutic targets. In summary, this study suggests clinically extensive, severe CCCA may have a differential gene expression pattern in the lesional scalp of affected patients, in addition to its clinical distinction.

Indexed as

AlopeciaDermatitisCicatrixFemaleGene Expression ProfilingHairHumansMicroarray AnalysisScalpalopeciacentral centrifugal cicatricial alopeciacicatricial alopeciafibroproliferative disordersfibrosis

Identifiers

PMID35007355
PMCPMC9127746
OpenAlexW4206762793

What OpenQuestion holds

Textmetadata
LicenceTDM
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.