Elevation of glycosaminoglycans in the amniotic fluid of a fetus with mucopolysaccharidosis VII
- PMID: 28207930
- PMCID: PMC5436936
- DOI: 10.1002/pd.5028
Elevation of glycosaminoglycans in the amniotic fluid of a fetus with mucopolysaccharidosis VII
Abstract
Objective: The aim of this study was to quantify glycosaminoglycans (GAGs) in amniotic fluid (AF) from an MPS VII fetus compared with age-matched fetuses obtained from normal pregnancies.
Method: Disaccharides were measured by liquid chromatography tandem mass spectrometry, compared to age-matched controls. Enzyme assay was performed in AF supernatant or cultured amniocytes. GUSB was analyzed by next generation sequencing using Ion Torrent Personal Genome Machine with a customized panel.
Results: No activity of β-glucuronidase was detected in fetal cells. The pregnancy was spontaneously terminated in the third trimester. Genetic studies identified a homozygous mutation of p.N379D (c.1135A > G) in the GUSB gene. Liquid chromatography tandem mass spectrometry showed that chondroitin sulfate, dermatan sulfate, heparan sulfate, and keratan sulfate levels were markedly increased in the MPS VII AF, compared to those in age-matched control AF (dermatan sulfate, heparan sulfate, and chondroitin-6-sulfate more than 10 × than age-matched controls; chondroitin-4-sulfate and keratan sulfate more than 3 times higher).
Conclusion: This is the first report of specific GAG analysis in AF from an MPS VII fetus, indicating that GAG elevation in AF occurs by 21 weeks of gestation and could be an additional tool for prenatal diagnosis of MPS VII and potentially other MPS types. © 2017 John Wiley & Sons, Ltd.
© 2017 John Wiley & Sons, Ltd.
Conflict of interest statement
Similar articles
-
Newborn screening and diagnosis of mucopolysaccharidoses.Mol Genet Metab. 2013 Sep-Oct;110(1-2):42-53. doi: 10.1016/j.ymgme.2013.06.007. Epub 2013 Jun 21. Mol Genet Metab. 2013. PMID: 23860310 Free PMC article. Review.
-
Histopathological diagnosis of a type vii mucopolysaccharidosis after pregnancy termination.Fetal Pediatr Pathol. 2009;28(1):1-8. doi: 10.1080/15513810802547943. Fetal Pediatr Pathol. 2009. PMID: 19116811
-
First human treatment with investigational rhGUS enzyme replacement therapy in an advanced stage MPS VII patient.Mol Genet Metab. 2015 Feb;114(2):203-8. doi: 10.1016/j.ymgme.2014.10.017. Epub 2014 Nov 7. Mol Genet Metab. 2015. PMID: 25468648 Free PMC article.
-
Rapid prenatal testing for human beta-glucuronidase deficiency (MPS VII).Genet Test. 2003 Fall;7(3):241-3. doi: 10.1089/109065703322537269. Genet Test. 2003. PMID: 14642000
-
Mutations and polymorphisms in GUSB gene in mucopolysaccharidosis VII (Sly Syndrome).Hum Mutat. 2009 Apr;30(4):511-9. doi: 10.1002/humu.20828. Hum Mutat. 2009. PMID: 19224584 Free PMC article. Review.
Cited by
-
Contribution of tandem mass spectrometry to the diagnosis of lysosomal storage disorders.J Inherit Metab Dis. 2018 May;41(3):457-477. doi: 10.1007/s10545-017-0126-3. Epub 2018 Mar 19. J Inherit Metab Dis. 2018. PMID: 29556840 Review.
-
Enzyme replacement therapy for mucopolysaccharidoses; past, present, and future.J Hum Genet. 2019 Nov;64(11):1153-1171. doi: 10.1038/s10038-019-0662-9. Epub 2019 Aug 27. J Hum Genet. 2019. PMID: 31455839 Review.
-
Prenatal Diagnosis of Mucopolysaccharidosis-Plus Syndrome (MPSPS).Genes (Basel). 2023 Aug 3;14(8):1581. doi: 10.3390/genes14081581. Genes (Basel). 2023. PMID: 37628632 Free PMC article.
-
Open-label phase 1/2 study of vestronidase alfa for mucopolysaccharidosis VII.Mol Genet Metab Rep. 2021 May 29;28:100774. doi: 10.1016/j.ymgmr.2021.100774. eCollection 2021 Sep. Mol Genet Metab Rep. 2021. PMID: 34136357 Free PMC article.
-
Diagnosis of Mucopolysaccharidoses.Diagnostics (Basel). 2020 Mar 22;10(3):172. doi: 10.3390/diagnostics10030172. Diagnostics (Basel). 2020. PMID: 32235807 Free PMC article. Review.
References
-
- Elizabeht Neufeld, Joseph Muenzer. The Mucopolysaccharidoses. New York: McGraw-Hill; 2001.
-
- Sly WS, Quinton BA, McAlister WH, Rimoin DL. Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis. J Pediatr. 1973;82(2):249–257. - PubMed
-
- Beaudet AL, DiFerrante NM, Ferry GD, et al. Variation in the phenotypic expression of beta-glucuronidase deficiency. J Pediatr. 1975;86(3):388–394. - PubMed
-
- Pfeiffer RA, Kresse H, Bäumer N, Sattinger E. Beta-glucuronidase deficiency in a girl with unusual clinical features. Eur J Pediatr. 1977;126(3):155–161. - PubMed
-
- Gitzelmann R, Wiesmann UN, Spycher MA, et al. Unusually mild course of beta-glucuronidase deficiency in two brothers (mucopolysaccharidosis VII) Helv Paediatr Acta. 1978;33(4–5):413–428. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical