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Extension of the Pompe mutation database by linking disease-associated variants to clinical severity.
Niño, Monica Y; In 't Groen, Stijn L M; Bergsma, Atze J; van der Beek, Nadine A M E; Kroos, Marian; Hoogeveen-Westerveld, Marianne; van der Ploeg, Ans T; Pijnappel, W W M Pim.
Afiliação
  • Niño MY; Department of Pediatrics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • In 't Groen SLM; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Bergsma AJ; Center for Lysosomal and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • van der Beek NAME; Department of Pediatrics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Kroos M; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Hoogeveen-Westerveld M; Center for Lysosomal and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • van der Ploeg AT; Department of Pediatrics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Pijnappel WWMP; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Hum Mutat ; 40(11): 1954-1967, 2019 11.
Article em En | MEDLINE | ID: mdl-31254424
Pompe disease is an autosomal recessive lysosomal storage disorder caused by disease-associated variants in the acid alpha-glucosidase (GAA) gene. The current Pompe mutation database provides a severity rating of GAA variants based on in silico predictions and expression studies. Here, we extended the database with clinical information of reported phenotypes. We added additional in silico predictions for effects on splicing and protein function and for cross reactive immunologic material (CRIM) status, minor allele frequencies, and molecular analyses. We analyzed 867 patients and 562 GAA variants. Based on their combination with a GAA null allele (i.e., complete deficiency of GAA enzyme activity), 49% of the 422 disease-associated variants could be linked to classic infantile, childhood, or adult phenotypes. Predictions and immunoblot analyses identified 131 CRIM negative and 216 CRIM positive variants. While disease-associated missense variants were found throughout the GAA protein, they were enriched up to seven-fold in the catalytic site. Fifteen percent of disease-associated missense variants were predicted to affect splicing. This should be confirmed using splicing assays. Inclusion of clinical severity rating in the Pompe mutation database provides an invaluable tool for diagnosis, prognosis of disease progression, treatment regimens, and the future development of personalized medicine for Pompe disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Depósito de Glicogênio Tipo II / Predisposição Genética para Doença / Bases de Dados Genéticas / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Depósito de Glicogênio Tipo II / Predisposição Genética para Doença / Bases de Dados Genéticas / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article