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1.
Clin Biochem ; 50(7-8): 431-435, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28088454

RESUMO

BACKGROUND: The goal of this study was to assess the biochemical parameters of the enzymes α-l-iduronidase (IDUA) and arylsulfatase B (ASB), which are deficient in mucopolysaccharidosis (MPS) I and VI, respectively, in dried blood spot (DBS) samples impregnated on filter paper. METHODS AND RESULTS: The optimal pH, Km, and Vmax of IDUA and ASB in DBS are hereby presented. After these analyses, the reference values for the activities of these enzymes in DBS with cutoff of 3.65nmol/h/mL for IDUA and 6.80nmol/h/mL for ASB were established. The research also showed that the stability (21days) of the IDUA activity is lower than ASB, which maintained its enzymatic activity stable up until 60days of analysis, after impregnating the filter paper with blood. CONCLUSION: Currently, DBS ensures important advantages in handling storage and transportation of samples with respect to neonatal screening programs. This study contributes to characterizing and differentiating the biochemistry of deficient enzymes in MPSs I and VI of DBS samples.


Assuntos
Teste em Amostras de Sangue Seco/métodos , Iduronidase/sangue , Mucopolissacaridose IV/sangue , Mucopolissacaridose I/sangue , N-Acetilgalactosamina-4-Sulfatase/sangue , Teste em Amostras de Sangue Seco/instrumentação , Feminino , Humanos , Masculino
2.
Gene ; 536(2): 344-7, 2014 Feb 25.
Artigo em Inglês | MEDLINE | ID: mdl-24342658

RESUMO

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.


Assuntos
Hidrolases/metabolismo , Doenças por Armazenamento dos Lisossomos/diagnóstico , Lisossomos/enzimologia , Lisossomos/metabolismo , Coleta de Amostras Sanguíneas , Feminino , Humanos , Doenças por Armazenamento dos Lisossomos/enzimologia , Doenças por Armazenamento dos Lisossomos/metabolismo , Masculino , Programas de Rastreamento/métodos
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