Abstract

In a study of eight glycosidases in serum samples from 72 cystic fibrosis patients, 85 cystic fibrosis parents and 34 healthy and diseased controls, significant elevations of mean α-glucosidase levels were found in cystic fibrosis patients. All other glycosidases did not show any significant change. Mean α-glucosidase levels in obligate heterozygotes were the same as in control individuals. Moreover, α-glucosidase levels in cystic fibrosis patients correlated with the degree of clinical impairment as measured by the Schwachman score.

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