The Journal of Pediatrics
Volume 153, Issue 6 , Pages 758-763.e1, December 2008

Diagnosis of Cystic Fibrosis by Sweat Testing: Age-Specific Reference Intervals

  • Avantika Mishra

      Affiliations

    • Department of Biochemical Genetics, VCGS Pathology, The Royal Children's Hospital, Parkville, Victoria, Australia
    • School of Medical Science–Laboratory Medicine, RMIT University, Bundoora, Victoria, Australia
  • ,
  • Ronda Greaves

      Affiliations

    • Laboratory Services—Complex Biochemistry, The Royal Children's Hospital, Parkville, Victoria, Australia
  • ,
  • Katherine Smith

      Affiliations

    • Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Victoria, Australia
  • ,
  • John B. Carlin

      Affiliations

    • Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Victoria, Australia
    • Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia
  • ,
  • Andrew Wootton

      Affiliations

    • School of Medical Science–Laboratory Medicine, RMIT University, Bundoora, Victoria, Australia
  • ,
  • Rob Stirling

      Affiliations

    • Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital, Melbourne, Victoria, Australia
  • ,
  • John Massie

      Affiliations

    • Department of Respiratory Medicine, The Royal Children's Hospital, Parkville, Victoria, Australia
    • Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia
    • Murdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Victoria, Australia
    • Corresponding Author InformationReprint requests: Associate Professor John Massie, Department of Respiratory Medicine, The Royal Children's Hospital, Parkville VIC 3052, Australia

Received 18 December 2007; received in revised form 25 February 2008; accepted 28 April 2008. published online 01 July 2008.

Objective

To develop reference intervals (RIs) for sweat chloride and sodium in healthy children, adolescents, and adults.

Study design

Healthy, unrelated subjects aged from 5 to >50 years and subjects who were pancreatic insufficient with cystic fibrosis (CF) were recruited. Sweat collection was performed on all subjects with the Wescor Macroduct system. Sweat electrolytes were analyzed with direct ion selective electrodes. ΔF508 mutation analysis was performed on the healthy subjects ≥15 years old.

Results

A total of 282 healthy and 40 subjects with CF were included for analysis. There was no overlap of sweat chloride between the group with CF and the group without CF, but there was some overlap of sweat sodium. Sweat chloride increased with age, with the rate of increase slowing progressively to zero after the age of 19 years. The estimated median (95% RI) for sweat chloride were: 5 to 9 years, 13 mmol/L (1-39 mmol/L); 10 to 14 years, 18mmol/L (3-47 mmol/L); 15 to 19 years, 20 mmol/L (3-51mmol/L); and 20+ years 23 mmol/L (5-56mmol/L).

Conclusions

We have successfully developed the age-related RI for sweat electrolytes, which will be useful for clinicians interpreting sweat test results from children, adolescents, and adults.

Abbreviations: CF, Cystic fibrosis, CFTR, Cystic fibrosis transmembrane conductance regulator, RI, Reference intervals

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 Supported by a Scientific Grant from the Australasian Association of Clinical Biochemists. The authors declare no conflicts of interest.

PII: S0022-3476(08)00375-2

doi:10.1016/j.jpeds.2008.04.067

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The Journal of Pediatrics
Volume 153, Issue 6 , Pages 758-763.e1, December 2008