Abstract
Sweat chlorides of 10 sets of parents of children with cystic fibrosis and 11 controls were studied in an attempt to develop a test for the diagnosis of cystic fibrosis heterozygotes by subjecting both the parents and controls to a low sodium diet and comparing sweat chloride values as the diet progressed. It was hoped that the sweat chloride levels of the parents, the heterozygotes, would remain stationary throughout the diet, since their children, the homozygotes, reveal this finding under similar conditions of salt deprivation. The sweat chloride levels of the controls, because of effects of aldosterone, were expected to decrease steadily from the commencement of the diet to its termination.
A decrease in sweat chloride values of similar magnitude was found in both parents and controls as the diet continued. It is concluded that the study of sweat electrolyte levels in salt-deprived subjects is of no value in the diagnosis of cystic fibrosis heterozygotes.
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Selected References
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- ANDERSON C. M., FREEMAN M. 'Sweat test' results in normal persons of different ages compared with families with fibrocystic disease of the pancreas. Arch Dis Child. 1960 Dec;35:581–587. doi: 10.1136/adc.35.184.581. [DOI] [PMC free article] [PubMed] [Google Scholar]