Evidence map›Paper›PMID 42813741›Full record

ArticleActa dermato-venereologica2026

Objectively Measured Photoaging and Skin Cancer in Organ Transplant Recipients.

Stine R Wiegell, Peter A Philipsen, Susanne K Kjær, Jay F Nash, Peter Bjerring, Merete Hædersdal

Abstract read
In one paragraph

Article in Acta dermato-venereologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

6 authors.

Stine R WiegellDepartment of Dermatology, Copenhagen University Hospital Bispebjerg, Copenhagen, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark. stine.regin.wiegell@regionh.dk.
Peter A PhilipsenDepartment of Dermatology, Copenhagen University Hospital Bispebjerg, Copenhagen, Denmark.ORCID 0000-0002-9656-733X
Susanne K KjærDepartment of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark; Unit of Virus, Lifestyle and Genes, Danish Cancer Institute, Copenhagen, Denmark; Juliane Marie Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-8347-1398
Jay F NashGlobal Product Stewardship, The Procter & Gamble Company, Mason, Ohio, United States.ORCID 0000-0001-6133-9639
Peter BjerringDepartment of Dermatology, Aalborg University Hospital, Aalborg, Denmark.ORCID 0000-0002-3031-1390
Merete HædersdalDepartment of Dermatology, Copenhagen University Hospital Bispebjerg, Copenhagen, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-1250-2035

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid organ transplant recipients (SOTRs) have an increased risk of keratinocyte skin cancer (KC) due to lifelong immunosuppression. Photoaging, reflecting cumulative ultraviolet (UV) exposure, may serve as a biomarker of KC risk. This study characterized objective photoaging features in SOTRs and their association with age, photodamage, photoaging phenotype, actinic keratoses (AKs) and KC history. In 251 SOTRs, VISIA imaging showed significant age-related increases in photoaging features; median red- feature scores reflecting erythema and telangiectasia were 44 AU (arbitrary units) in patients >60 vs 22 AU in those <60. Higher clinical photodamage severity corresponded to higher VISIA scores, especially red- features and visible- spots. The atrophic photoaging phenotype, observed in 60 % of patients, showed higher red- features (40 AU) than the hypertrophic type (27 AU). Patients with AKs had elevated UV- spots and red- features. A history of KC (32 % of participants) was associated with older age, longer time since transplantation, fairer skin type, more severe photodamage, higher VISIA scores, especially red- features (45 AU vs 29 AU) and greater pigmentation on sun-exposed sites. Objective imaging identified photoaging features associated with cumulative UV damage. Further studies should evaluate their predictive value for KC development to improve individualized risk stratification and surveillance strategies in this high-risk population.

Indexed as

Immunosuppressive AgentsKeratosis, ActinicNeoplasms, Radiation-InducedOrgan TransplantationSkinSkin AgingSkin NeoplasmsAdultAgedAge FactorsFemaleHumansImmunocompromised HostMaleMiddle AgedPhenotypeImmunosuppressive Agents

Identifiers

PMID42813741
PMCPMC13625172

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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.