Infant palmar hyperlinearity and type 2 inflammatory markers predict atopic dermatitis at 1year of age

Iben Frier Ruge1,2, Anne-Sofie Halling1,2, Maria Rasmussen Rinnov2,3

  • 1Department of Dermatology and Venereology, Bispebjerg Hospital, Bispebjerg and Frederiksberg Hospital, University of Copenhagen, Copenhagen, Denmark.

Insights

Hyperlinear palms in infants are linked to a higher risk of developing atopic dermatitis (AD) within the first two years of life. Early signs of inflammation can further increase this risk, aiding in early AD detection.

Area of Science:

  • Dermatology
  • Pediatrics
  • Immunology

Background:

  • Identifying early predictors for pediatric atopic dermatitis (AD) is crucial for prevention.
  • Hyperlinear palms, a clinical sign, are associated with filaggrin gene (FLG) mutations and AD.
  • Understanding palmar phenotypes in infancy may reveal links to childhood AD.

Purpose of the Study:

  • To determine if distinct palmar phenotypes in infancy predict the onset of AD in early childhood.
  • To investigate the association between infant palmar crease patterns and the development of AD.

Main Methods:

  • A cohort of 300 term and 150 preterm newborns were clinically monitored for AD up to age 2.
  • Palmar photographs were taken at 2 months for blinded assessment; FLG mutations and biomarkers (TARC/CCL17) were analyzed.
  • Hazard ratios (HR) were calculated to assess the risk of AD development.

Main Results:

  • Hyperlinear palms at 2 months were present in 14.3% of infants and significantly associated with increased AD occurrence by age 1 and 2.
  • This association persisted after adjusting for FLG mutation status.
  • The combination of hyperlinear palms and elevated TARC/CCL17 at 2 months further increased AD risk in term infants by age 2.

Conclusions:

  • Hyperlinear palms observed at 2 months of age are a significant indicator of paediatric AD risk within the first year.
  • The presence of type 2 inflammation markers at 2 months, alongside hyperlinear palms, amplifies the risk of developing AD.
Abstract