Journal of Inherited Metabolic Disease · 2007 · 31 citations · 9 references
MedicineBiochemistryMolecular MedicineClinical BiochemistryHepatologyMolecular DiagnosticsBiomarkers Of Liver InjuryChronic Liver DiseaseHepatic PathophysiologyLiver DiseaseLiver Function TestsMetabolic Liver DiseaseBiotinidase DeficiencyGlycogen Storage DiseasesGlycogen Storage In LiverHepatic BiomarkersHepatic DisordersLiver BiomarkersSerum Enzyme Activity Measurement
An elevated serum biotinidase activity in patients with glycogen storage disease (GSD) type Ia has been reported previously. The aim of this work was to investigate the specificity of the phenomenon and thus we expanded the study to other types of hepatic GSDs. Serum biotinidase activity was measured in a total of 68 GSD patients and was compared with that of healthy controls (8.7 +/- 1.0; range 7.0-10.6 mU/ml; n = 26). We found an increased biotinidase activity in patients with GSD Ia (17.7 +/- 3.9; range: 11.4-24.8; n = 21), GSD I non-a (20.9 +/- 5.6; range 14.6-26.0; n = 4), GSD III (12.5 +/- 3.6; range 7.8-19.1; n = 13), GSD VI (15.4 +/- 2.0; range 14.1-17.7; n = 3) and GSD IX (14.0 +/- 3.8; range: 7.5-21.6; n = 22). The sensitivity of this test was 100% for patients with GSD Ia, GSD I non-a and GSD VI, 62% for GSD III, and 77% for GSD IX, indicating reduced sensitivity for GSD III and GSD IX, respectively. In addition, we found elevated biotinidase activity in all sera from 5 patients with Fanconi-Bickel Syndrome (15.3 +/- 3.7; range 11.0-19.4). Taken together, we propose serum biotinidase as a diagnostic biomarker for hepatic glycogen storage disorders.
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The estimation of glycogen with the anthrone reagent.
Sam Seifter, S Dayton · PubMed · 1950 · 1.4K citations
B Lederer, F. Van Hoof, Greet Van den Berghe · Biochemical Journal · 1975 · 81 citations · Full text