Aquagenic wrinkling of the palms in cystic fibrosis: comparison with controls and genotype-phenotype correlations

Arch Dermatol. 2009 Nov;145(11):1296-9. doi: 10.1001/archdermatol.2009.260.

Abstract

Objective: To determine the prevalence of aquagenic wrinkling of the palms (AWP) in patients with cystic fibrosis (CF) compared with control patients, and evaluate for genotype-phenotype correlations. Since its first description over 30 years ago, AWP has frequently been anecdotally associated with CF, but this association has not been confirmed in a rigorous prospective case-control study.

Design: Blinded comparison.

Setting: The CF and dermatology clinics at St Louis Children's Hospital.

Participants: Forty-four individuals with CF from a CF clinic and 26 controls from a dermatology clinic. Intervention Participants were tested for AWP using 3 minutes of water immersion with room-temperature tap water. Main Outcome Measure The degree of AWP was scored from 0 (no wrinkling) to 4 (severe wrinkling) by 3 blinded physicians. For genotype-phenotype correlations, patients with CF were divided into those homozygous for the DeltaF508 mutation and those with other genotypes.

Results: The mean AWP score of the CF group was significantly higher than the mean score of the control group (1.5 vs 0.6; P < .001). Patients with CF who were homozygous for the DeltaF508 mutation (n = 27) had significantly higher scores than patients with CF who were not homozygous for the DeltaF508 mutation (n = 17) (1.7 vs 1.1; P = .02). The 17 patients with CF who were not homozygous for the DeltaF508 mutation still had higher scores than the control group (1.1 vs 0.6; P = .03). There was no correlation between sweat chloride concentrations measured at the time of diagnosis and AWP score.

Conclusions: Our results confirm the association between AWP and CF. Among patients with CF, greater AWP occurs in those who are homozygous for the DeltaF508 mutation.

Publication types

  • Comparative Study

MeSH terms

  • Age Distribution
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Confidence Intervals
  • Cystic Fibrosis / epidemiology*
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis / physiopathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Female
  • Genetic Predisposition to Disease / epidemiology*
  • Genetic Testing
  • Genotype
  • Hand*
  • Humans
  • Incidence
  • Male
  • Phenotype
  • Probability
  • Reference Values
  • Severity of Illness Index
  • Sex Distribution
  • Skin Aging / genetics*

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator