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Newborn screening for mucopolysaccharidoses: Measurement of glycosaminoglycans by LC-MS/MS

Authors :
Molly Stapleton
Francyne Kubaski
Robert W. Mason
Haruo Shintaku
Hironori Kobayashi
Seiji Yamaguchi
Takeshi Taketani
Yasuyuki Suzuki
Kenji Orii
Tadao Orii
Toshiyuki Fukao
Shunji Tomatsu
Source :
Molecular Genetics and Metabolism Reports, Vol 22, Iss , Pp - (2020)
Publication Year :
2020
Publisher :
Elsevier, 2020.

Abstract

Mucopolysaccharidoses (MPS) are a family of lysosomal storage disorders which can lead to degenerative and irreversible skeletal, cardiovascular, pulmonary, and neurological damage. Current treatments, including hematopoietic stem cell transplantation and enzyme replacement therapy, have been found most effective if administered before clinical symptoms are present, highlighting the urgent need for the development of newborn screening.This study analyzed 18,222 dried blood spot samples from newborns for both enzyme activity and glycosaminoglycan (GAG) concentration levels. GAG levels were measured using liquid chromatography tandem mass spectrometry. Results were compared to our previously established cutoff values for three subtypes of GAGs: dermatan sulfate (DS) and heparan sulfate (HS0S and HSNS). Samples that were high for two of the three GAGs were identified and screened a second time. Samples were also measured for iduronate-2-sulfatase and alfa-L-iduronidase activity.A total of 300 samples were above the established cutoff values for at least two of the three GAGs after the first screening. One sample was determined through clinical and genetic testing to be a true positive for MPS II. The false positive rate after the first GAG screening was 1.64%. A Cochran's formula test showed that the samples available for the second screening were representative samples (p = .0000601). False positive rate after second GAG screening, extrapolated from the representative sample was 0.4%. False positive rate after enzyme activity assay by fluorimetry for IDUA and IDS enzymes was 0.21% and 0.18%. A combination of GAG and enzyme assays provided no false positive and false negative samples.Two-tier screening involving a combination of enzyme activity and multiple GAGs should be considered the gold standard for the diagnosis of MPS patients. Keywords: Newborn screening, Mucopolysaccharidosis, Fetal GAG contamination, Tandem mass spectrometry, Glycosaminoglycans

Details

Language :
English
ISSN :
22144269
Volume :
22
Issue :
-
Database :
Directory of Open Access Journals
Journal :
Molecular Genetics and Metabolism Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.b40847e2cc744d6497014a2d4ca0d659
Document Type :
article
Full Text :
https://doi.org/10.1016/j.ymgmr.2019.100563