[MC1R polymorphisms and facial photoaging]

Ann Dermatol Venereol. 2011 May;138(5):385-9. doi: 10.1016/j.annder.2011.02.026. Epub 2011 Apr 29.
[Article in French]

Abstract

Background: The objective of this study was to assess the association between melanocortin-1 receptor (MC1R) variants and the severity of facial skin photoaging.

Methods: The study population comprised 530 French middle-aged women between 44 and 70 years. A trained dermatologist graded the severity of facial skin photoaging from photographs using Larnier's global scale. Logistic regressions were performed to assess the influence of MC1R polymorphism on severe photoaging (grades 1-3 vs. 4-6), with adjustment for possible confounders (demographic and phenotypic data, and sun exposure intensity).

Results: Overall, 35% of the women were wild-type homozygotes, 49% had one variant, 15% had two variants, and 1% had at least one rare variant. After adjustment for possible confounders, the presence of two major diminished function variants was found to be a risk factor for photoaging (adjusted odds ratio=5.61; 95% confidence interval [1.43-21.96]).

Discussion: Our results suggest that genetic variations of MC1R are important determinants for severe photoaging.

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Confounding Factors, Epidemiologic
  • Female
  • France
  • Genetic Predisposition to Disease
  • Genotype
  • Habits
  • Humans
  • Middle Aged
  • Phenotype
  • Pigmentation
  • Polymorphism, Genetic*
  • Receptor, Melanocortin, Type 1 / genetics*
  • Receptor, Melanocortin, Type 1 / physiology
  • Risk Factors
  • Skin Aging / genetics*
  • Skin Aging / radiation effects
  • Sunlight

Substances

  • Receptor, Melanocortin, Type 1