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Evaluation of Two Methods for Quantification of Glycosaminoglycan Biomarkers in Newborn Dried Blood Spots from Patients with Severe and Attenuated Mucopolysaccharidosis Type II.
Herbst, Zackary M; Urdaneta, Leslie; Klein, Terri; Burton, Barbara K; Basheeruddin, Khaja; Liao, Hsuan-Chieh; Fuller, Maria; Gelb, Michael H.
Afiliação
  • Herbst ZM; Department of Chemistry, University of Washington, Seattle, WA 98195, USA.
  • Urdaneta L; Department of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Klein T; National MPS Society, P.O. Box 14686, Durham, NC 27707-4686, USA.
  • Burton BK; National MPS Society, P.O. Box 14686, Durham, NC 27707-4686, USA.
  • Basheeruddin K; Genetics, Birth Defects & Metabolism at Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
  • Liao HC; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
  • Fuller M; Newborn Screening Laboratory, Illinois Department of Public Health, Chicago, IL 60604, USA.
  • Gelb MH; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98195, USA.
Int J Neonatal Screen ; 8(1)2022 Jan 21.
Article em En | MEDLINE | ID: mdl-35225932
ABSTRACT
All newborn screening (NBS) for mucopolysaccharidosis-I and -II (MPS-I and MPS-II) is carried out via the measurement of α-iduronidase (IDUA) and iduronate-2-sulfatase (IDS) enzymatic activity, respectively, in dried blood spots (DBS). The majority of low enzyme results are due to pseudodeficiencies, and data from recent MPS-II population screenings and studies from the Mayo Clinic show that the false positive rate can be dramatically reduced by the inclusion of a second-tier analysis of glycosaminoglycans (GAGs) in DBS as part of NBS. In the present study, which focused on MPS-II, we obtained newborn DBS from 17 patients with severe MPS-II, 1 with attenuated MPS-II, and 6 patients with various IDS pseudodeficiencies. These samples were submitted to two different GAG mass spectrometry analyses in a comparative study (1) internal disaccharide biomarkers and (2) endogenous biomarkers. For both of these methods, the biomarker levels in six patients with pseudodeficiencies were below the range measured in MPS-II patients. One patient with attenuated MPS-II was not distinguishable from severe disease patients, but all MPS-II patients were distinguishable from the reference range using both methods. The minimal differential factor (lowest GAG marker level in MPS-II samples divided by highest level in the reference range of 60 random newborns) was 3.01-fold for the internal disaccharide method. The endogenous biomarker method demonstrated an improved minimum differential of 5.41-fold. The minimum differential factors between MPS-II patients and patients with pseudodeficiencies for the internal disaccharide and endogenous biomarker methods were 3.77-fold and 2.06-fold, respectively. This study supports use of the second-tier GAG analysis of newborn DBS, especially the endogenous disaccharide method, as part of NBS to reduce the false positive rate.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article