Evidence map›Paper›PMID 40771400›Full record

ArticleFrontiers in aging2025

Identification of gene-sun exposure interactions of GWAS-identified variants in perceived facial aging progression.

Ludivine Obry, Raissa Medina-Santos, Myriam Rahmouni, Josselin Noirel, Toufik Labib, Pilar Galan, Jean-Louis Spadoni, Gaëlle Gendronneau, Randa Jdid, Sandra Courrèges and 4 more

Abstract read
In one paragraph

Article in Frontiers in aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Ludivine Obry *Laboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Raissa Medina-Santos *Laboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Myriam RahmouniLaboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Josselin NoirelLaboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Toufik LabibLaboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Pilar GalanEquipe de Recherche en Epidémiologie Nutritionnelle (EREN), Centre d'Epidemiologie et Biostatistiques Sorbonne Paris Cité (CRESS), Inserm U1153, Inra U1125, Cnam, Université Sorbonne Paris Nord et Sorbonne-Paris-Cité, Paris, France.
Jean-Louis SpadoniLaboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Gaëlle GendronneauBiological and Clinical Department, IRD Chanel Fragrance & Beauty, Bobigny, France.
Randa JdidBiological and Clinical Department, IRD Chanel Fragrance & Beauty, Bobigny, France.
Sandra CourrègesBiological and Clinical Department, IRD Chanel Fragrance & Beauty, Bobigny, France.
Julie LatreilleBiological and Clinical Department, IRD Chanel Fragrance & Beauty, Bobigny, France.
Nada AndréBiological and Clinical Department, IRD Chanel Fragrance & Beauty, Bobigny, France.
Jean-François ZaguryLaboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.
Sigrid Le ClercLaboratoire Génomique, Bioinformatique, et Chimie Moléculaire, EA7528, Conservatoire National des Arts et Métiers, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Skin aging is characterized by observable major changes in the composition and organization of the skin, including the appearance of wrinkles, tissue sagging, dryness, and pigmentary disorders. While both environmental and genetic factors contribute to these changes, their interaction remains underexplored. Perceived age is a biomarker of health and strongly related to facial skin aging features. Thus, we conducted a gene-environment interaction analysis on the perceived facial aging progression phenotype in 226 women, focusing on sun exposure as the environmental factor. Methods: We assessed perceived age in 226 women at two time points, 12 years apart, allowing defining a perceived facial aging progression as phenotype. We applied a two-step gene-environment interaction approach. First, a genome-wide association study (GWAS) was performed to identify SNP effects on the perceived facial aging progression, selecting those with a Result: The GWAS identified four significant SNP associated with perceived facial aging progression, located in the Discussion: This study revealed four relevant genetic associations with skin aging and one significant G × E interaction. These findings support the known link between telomere shortening/protection and aging, and suggesting a potential role for keratinization in the context of facial aging and sun exposure, though further validation in larger cohorts is necessary. The findings could help to develop new approaches for facial aging prevention and treatment and to better understand molecular mechanisms of aging.

Indexed as

facial agingG×E interactionGWASperceived ageSNPsun exposure

Identifiers

PMID40771400
PMCPMC12326137

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.