Evidence map›Paper›PMID 41647765›Full record

ReviewThe Journal of clinical and aesthetic dermatology2025

PDE4 Inhibitor-Responsive Dermatoses: An Emerging Concept in Dermatology.

Courtney A Chau, Hilary E Baldwin, James Q Del Rosso, Julie C Harper, Edward Lain, Todd Schlesinger, Ali Shahbaz, Heather Woolery-Lloyd, Jennifer C Jaworski, Melissa S Seal and 2 more

Abstract readReview
In one paragraph

Review in The Journal of clinical and aesthetic dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Courtney A ChauMs. Chau is with the Icahn School of Medicine at Mount Sinai in New York, New York.
Hilary E BaldwinDr. Baldwin is with the Department of Dermatology at Rutgers University Robert Wood Johnson Medical Center in New Brunswick, New Jersey.
James Q Del RossoDr. Del Rosso is with JDR Dermatology Research Center, LLC in Las Vegas, Nevada and Advanced Dermatology and Cosmetic Surgery in Maitland, Florida.
Julie C HarperDr. Harper is with the Dermatology and Skin Care Center of Birmingham in Birmingham, Alabama.
Edward LainDr. Lain is with Sanova Dermatology in Austin, Texas.
Todd SchlesingerDr. Schlesinger is with Clinical Research Center of the Carolinas in Charleston, South Carolina.
Ali ShahbazDr. Shahbaz is with Texas A&M School of Medicine in Bryan, Texas and Westlake Dermatology and Cosmetic Surgery in Austin, Texas.
Heather Woolery-LloydDr. Woolery-Lloyd is with the Dr. Philip Frost Department of Dermatology and Cutaneous Surgery at the University of Miami Miller School of Medicine in Miami, Florida.
Jennifer C JaworskiMs. Jaworski, Dr. Seal, and Dr. Hanna are with Arcutis Biotherapeutics, Inc. in Westlake Village, California.
Melissa S SealMs. Jaworski, Dr. Seal, and Dr. Hanna are with Arcutis Biotherapeutics, Inc. in Westlake Village, California.
Diane HannaMs. Jaworski, Dr. Seal, and Dr. Hanna are with Arcutis Biotherapeutics, Inc. in Westlake Village, California.
Peter LioDr. Lio is with the Departments of Dermatology & Pediatrics at Northwestern University Feinberg School of Medicine in Chicago, Illinois.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many inflammatory skin conditions share mechanistic pathways involving multiple receptors and cytokines. Perhaps there is no better endorsement of this idea than the foundational concept of "steroid-responsive dermatoses." Similarly, targeting the phosphodiesterase 4 (PDE4) enzyme, which exists at the crux of several pathways that contribute to inflammatory skin diseases, offers an avenue by which the pathogenesis of multiple conditions may be interrupted. This suggests that PDE4 inhibitors may assume a similar complementary framework for treating "PDE4 inhibitor-responsive dermatoses." Certain formulations of PDE4 inhibitors (including apremilast, crisaborole, and roflumilast) have undergone rigorous investigation in clinical trials and demonstrated robust efficacy and safety in many dermatologic conditions, achieving United States Food and Drug Administration approval for atopic dermatitis, psoriasis, and seborrheic dermatitis. Herein, we summarize the clinical evidence supporting the emerging concept of "PDE4 inhibitor-responsive dermatoses" and propose that PDE4 inhibition offers an additional pathway to achieving desired clinical outcomes.

Indexed as

apremilastcrisaborolePDE4 inhibitor-responsive dermatosesphosphodiesterase 4 inhibitionroflumilastSteroid-responsive dermatoses

Identifiers

PMID41647765
PMCPMC12871500

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.