Evidence map›Paper›PMID 35279741›Full record

Trial reportArchives of dermatological research2023

Apremilast and narrowband ultraviolet B combination therapy suppresses Th17 axis and promotes melanogenesis in vitiligo skin: a randomized, split-body, pilot study in skin types IV-VI.

Hee J Kim, Ester Del Duca, Ana B Pavel, Giselle K Singer, Brian J Abittan, Margot A Chima, Grace Kimmel, Jennifer Bares, Danielle Baum, Matthew Gagliotti and 4 more

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Archives of dermatological research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. PDE4 Inhibitor-Responsive Dermatoses: An Emerging Concept in Dermatology.The Journal of clinical and aesthetic dermatology · 2025
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Vitiligo, from Pathogenesis to Therapeutic Advances: State of the Art.International journal of molecular sciences · 2023
    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

14 authors at 2 institutions in 1 country.

Hee J KimDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA. hee.kim@mountsinai.org.ORCID http://orcid.org/0000-0002-0546-6913
Ester Del DucaDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Ana B PavelDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Giselle K SingerDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Brian J AbittanDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Margot A ChimaDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Grace KimmelDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Jennifer BaresDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Danielle BaumDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Matthew GagliottiDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Jordan GeneceDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Justin ChuDepartment of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Mark G Lebwohl *Department of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Emma Guttman-Yassky *Department of Dermatology, Icahn School of Medicine and Mount Sinai, New York, NY, 10029, USA.
Icahn School of Medicine at Mount Sinai · USUniversity of Mississippi · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Improved repigmentation of generalized vitiligo in skin types IV-VI has been reported in clinical response to combined therapy with apremilast and narrowband (NB)-UVB; however, tissue responses to combined therapy versus NB-UVB monotherapy have not been elucidated. We compared the change from baseline in cellular and molecular markers in vitiligo skin after combined therapy versus NB-UVB monotherapy. We assessed lesional and nonlesional skin samples from enrolled subjects and evaluated for immune infiltrates, inflammatory, and melanogenesis-related markers which were compared across different treatment groups. Combined therapy resulted in significant reduction of CD8

Indexed as

Ultraviolet TherapyVitiligoCombined Modality TherapyHumansPilot ProjectsSkinThalidomideTreatment OutcomeapremilastThalidomideAnti-inflammatoryApremilastIFNγ pathwayInnate immune systemNarrowband UVBPhosphodiesterase-4 inhibitorSplit-body studyTh17 axisVitiligo

Identifiers

PMID35279741
OpenAlexW4220932339

What Socratic 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 Socratic graph.