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Determination of the lysosomal hydrolase activity in blood collected on filter paper,an alternative to screen high risk populations
Authors:Cristina D. Castilhos,Jamila MezzaliraMariana P.S. Goldim,Vanessa V. DaitxCristina da S. Garcia,Carla V. AndradeAna C. Breier,Jaqueline Cé  Alexandre S. Mello,Janice C. Coelho
Affiliation:Postgraduate Program, Biochemistry Department, Lysosomal Storage Diseases Testing Laboratory, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil
Abstract:This study aimed to determine the enzymatic activity in dried blood samples collected on filter paper (DBS) for the diagnosis of the following diseases: Fabry, Pompe, Mucopolysaccharidosis type I (MPS I) and Mucopolysaccharosis type VI (MPS VI). DBS was used for high risk patientscreening, according to clinical suspicion. Plasma, leukocytes and cultured fibroblasts were used to confirm the diagnosis when necessary. Among the 529 DBS samples sent to the laboratory, 164 had abnormal results. Confirmatory materials of 73 individuals were rerouted. The frequency of diagnosis for lysosomal storage disorders was 5.9%. DBS is an alternative screening technique used in high risk populations, which should lead to earlier diagnosis for lysosomal storage disorders (LSDs), help patients get treatment sooner and improve the outcome of the disease.
Keywords:DBS, Dried blood spots collected on filter paper   MPS I, Mucopolysaccharidosis type I   MPS VI, Mucopolysaccharosis type VI   LSDs, Lysosomal storage disorders   LC/MS/MS, Liquid chromatography combined with tandem mass spectrometry   GAL, Alpha-galactosidase A   GAA, Alpha-glucosidase   ASB, Arylsulphatase B   IDUA, Alpha-iduronidase   ROC, Receiver Operating Characteristics
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