Sweat conductivity test: can it replace chloride titration for cystic fibrosis diagnosis?


Cinel G., DOĞRU ERSÖZ D. , Yalcin E., Ozcelik U., Gurcan N., Kiper N.

TURKISH JOURNAL OF PEDIATRICS, vol.54, no.6, pp.576-582, 2012 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 54 Issue: 6
  • Publication Date: 2012
  • Title of Journal : TURKISH JOURNAL OF PEDIATRICS
  • Page Numbers: pp.576-582

Abstract

Although sweat conductivity values are well matched with chloride concentrations for cystic fibrosis (CF) diagnosis, sweat conductivity is not accepted as a definitive diagnostic tool but only a screening method. The aim of this study was to compare the sweat chloride measurements and sweat conductivity values of our patients, and to determine cut-off values of conductivity for making or excluding a CF diagnosis. Fifty-nine CF patients, 10 patients with elevated sweat tests and 69 non-CF patients were included in the study. The mean conductivity values were 123 (64-157) mmol/L, 75.1 (60-93) mmol/L and 39 (18-83) mmol/L in the CF, elevated sweat test and control groups, respectively. The mean chloride concentration values were 107.5 (35-166) mEq/L, 48 (42-76) mEq/L and 25 (11-39) mEq/L in the CF, elevated sweat test and control groups, respectively. Spearman correlation test determined a strong correlation between conductivity and chloride concentration values (r=88%, p<0.001) in all subjects. According to the receiver operating characteristic (ROC) curve graph, the best conductivity cut-off value to make the CF diagnosis was found to be 90 mmol/L and to exclude the CF diagnosis was 70 mmol/L. We suggest that the conductivity measurement is as reliable as quantitative sweat chloride analysis to diagnose or exclude CF, and it can be used as a diagnostic test in addition to screening.