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Published on: September 13, 2018
Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals
Avantika Mishra1, Ronda Greaves, Katherine Smith
1Department of Biochemical Genetics, VCGS Pathology, The Royal Children's Hospital, Parkville, Victoria, Australia.
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. DeltaF508 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.
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