RELIABLE DIAGNOSIS OF THE MAJOR TYPE OF CYSTIC FIBROSIS WITH FIBROBLAST CULTURES A Double Blind Study
- 1 September 1978
- journal article
- research article
- Published by Wiley in Acta Paediatrica
- Vol. 67 (5), 617-620
- https://doi.org/10.1111/j.1651-2227.1978.tb17812.x
Abstract
A double blind study was carried out to demonstrate that the most common type of cystic fibrosis (CF) can be reliably diagnosed with skin-derived fibroblast cultures. Alkaline phosphatase (AIP) activity was measured in 6 normal controls, 12 CF-heterozygotes and 6 CF-homozygotes before and after stimulation with Tamm-Horsfall-glycoprotein (THP), isoproterenol and theophylline (THP-induction test). The mean AIP-activities after THP-induction were 8.8, 12.7 and 34.6 for the 3 different genotypes, respectively. There was no overlap between the values of CF-homozygotes on 1 hand, and the values of CF-heterozygotes and normal controls on the other. All 24 specimens were correctly diagnosed in the present double blind study, indicating the high degree of reliability of the THP-induction test in the detection of the predominant type of cystic fibrosis with fibroblast cultures. Normal controls and CF-heterozygotes could not be discriminated on an individual basis, but as a group the CF-heterozygotes displayed higher AIP-values.This publication has 13 references indexed in Scilit:
- Reliable detection of cystic fibrosis in skin-derived fibroblast culturesHuman Genetics, 1978
- Cystic fibrosis: Leakage of lysosomal enzymes and of alkaline phosphatase into the extracellular spaceBiochemical and Biophysical Research Communications, 1977
- Prospects for prenatal diagnosis of cystic fibrosis: Induction of biochemical abnormalities in fibroblasts from patients with cystic fibrosis by a urinary glycoproteinBiochemical and Biophysical Research Communications, 1976
- A CLINICAL STUDY OF THE DIAGNOSIS OF CYSTIC FIBROSIS BY INSTRUMENTAL NEUTRON ACTIVATION ANALYSIS OF SODIUM IN NAIL CLIPPINGSActa Paediatrica, 1974
- A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomesBiochemical and Biophysical Research Communications, 1972
- I-CELL DISEASE : MULTIPLE LYSOSOMAL-ENZYME DEFECTThe Lancet, 1971
- Glycogen content of tissue culture fibroblasts from patients with cystic fibrosis and other heritable disordersThe Journal of Pediatrics, 1970
- Ultrastructure of cultivated fibroblasts in cystic fibrosis of the pancreasThe Journal of Pediatrics, 1970
- CYSTIC FIBROSIS OF THE PANCREASThe Journal of Experimental Medicine, 1969
- Acid mucopolysaccharides in cultured fibroblasts of cystic fibrosis of the pancreasBiochemical and Biophysical Research Communications, 1968