Skip to main content
Top
Published in: Journal of Inherited Metabolic Disease 1/2017

01-01-2017 | Original Article

Newborn screening for mucopolysaccharidoses: a pilot study of measurement of glycosaminoglycans by tandem mass spectrometry

Authors: Francyne Kubaski, Robert W. Mason, Akiko Nakatomi, Haruo Shintaku, Li Xie, Naomi N. van Vlies, Heather Church, Roberto Giugliani, Hironori Kobayashi, Seiji Yamaguchi, Yasuyuki Suzuki, Tadao Orii, Toshiyuki Fukao, Adriana M. Montaño, Shunji Tomatsu

Published in: Journal of Inherited Metabolic Disease | Issue 1/2017

Login to get access

Abstract

Background

Mucopolysaccharidoses (MPS) are a group of inborn errors of metabolism that are progressive and usually result in irreversible skeletal, visceral, and/or brain damage, highlighting a need for early diagnosis.

Methods

This pilot study analyzed 2862 dried blood spots (DBS) from newborns and 14 DBS from newborn patients with MPS (MPS I, n = 7; MPS II, n = 2; MPS III, n = 5). Disaccharides were produced from polymer GAGs by digestion with chondroitinase B, heparitinase, and keratanase II. Heparan sulfate (0S, NS), dermatan sulfate (DS) and mono- and di-sulfated KS were measured by liquid chromatography tandem mass spectrometry (LC-MS/MS). Median absolute deviation (MAD) was used to determine cutoffs to distinguish patients from controls. Cutoffs were defined as median + 7× MAD from general newborns.

Results

The cutoffs were as follows: HS-0S > 90 ng/mL; HS-NS > 23 ng/mL, DS > 88 ng/mL; mono-sulfated KS > 445 ng/mL; di-sulfated KS > 89 ng/mL and ratio di-KS in total KS > 32 %. All MPS I and II samples were above the cutoffs for HS-0S, HS-NS, and DS, and all MPS III samples were above cutoffs for HS-0S and HS-NS. The rate of false positives for MPS I and II was 0.03 % based on a combination of HS-0S, HS-NS, and DS, and for MPS III was 0.9 % based upon a combination of HS-0S and HS-NS.

Conclusions

Combination of levels of two or more different GAGs improves separation of MPS patients from unaffected controls, indicating that GAG measurements are potentially valuable biomarkers for newborn screening for MPS.
Appendix
Available only for authorised users
Literature
go back to reference Auclair D, Hopwood JJ, Brooks DA et al (2003) Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy. Mol Genet Metab 78:163–174CrossRefPubMed Auclair D, Hopwood JJ, Brooks DA et al (2003) Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy. Mol Genet Metab 78:163–174CrossRefPubMed
go back to reference Baldo G, Matte U, Artigalas O et al (2011) Placenta analysis of prenatally diagnosed patients reveals early GAG storage in mucopolysaccharidoses II and VI. Mol Genet Metab 103:197–198CrossRefPubMed Baldo G, Matte U, Artigalas O et al (2011) Placenta analysis of prenatally diagnosed patients reveals early GAG storage in mucopolysaccharidoses II and VI. Mol Genet Metab 103:197–198CrossRefPubMed
go back to reference Baldo G, Mayer FQ, Martinelli BZ et al (2013) Enzyme replacement therapy started at birth improves outcome in difficult-to-treat organs in mucopolysaccharidosis I mice. Mol Genet Metab 109:33–40CrossRefPubMed Baldo G, Mayer FQ, Martinelli BZ et al (2013) Enzyme replacement therapy started at birth improves outcome in difficult-to-treat organs in mucopolysaccharidosis I mice. Mol Genet Metab 109:33–40CrossRefPubMed
go back to reference Beck M, Braun S, Coerdt W et al (1992) Fetal presentation of Morquio disease type A. Prenat Diagn 12:1019–1029CrossRefPubMed Beck M, Braun S, Coerdt W et al (1992) Fetal presentation of Morquio disease type A. Prenat Diagn 12:1019–1029CrossRefPubMed
go back to reference Blanchard S, Sadilek M, Scott CR et al (2008) Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis I. Clin Chem 54:2067–2070CrossRefPubMedPubMedCentral Blanchard S, Sadilek M, Scott CR et al (2008) Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis I. Clin Chem 54:2067–2070CrossRefPubMedPubMedCentral
go back to reference Chace DH, Hannon WH (2010) Impact of second-tier testing on the effectiveness of newborn screening. Clin Chem 56:1653–1655CrossRefPubMed Chace DH, Hannon WH (2010) Impact of second-tier testing on the effectiveness of newborn screening. Clin Chem 56:1653–1655CrossRefPubMed
go back to reference de Ruijter J, Minke HR, Wagemans T et al (2012) Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses type I, II and III. Mol Genet Metab 107:705–710CrossRefPubMed de Ruijter J, Minke HR, Wagemans T et al (2012) Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses type I, II and III. Mol Genet Metab 107:705–710CrossRefPubMed
go back to reference Gabrielli O, Clarke LA, Bruni S et al (2010) Enzyme-replacement therapy in a 5-month-old boy with attenuated presymptomatic MPS I: 5-year follow-up. Pediatrics 125:183–187CrossRef Gabrielli O, Clarke LA, Bruni S et al (2010) Enzyme-replacement therapy in a 5-month-old boy with attenuated presymptomatic MPS I: 5-year follow-up. Pediatrics 125:183–187CrossRef
go back to reference Gelb MH, Turecek F, Scott CR et al (2006) Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders. J Inherit Metab Dis 29:397–404CrossRefPubMedPubMedCentral Gelb MH, Turecek F, Scott CR et al (2006) Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders. J Inherit Metab Dis 29:397–404CrossRefPubMedPubMedCentral
go back to reference Gelb MH, Scott CR, Turecek F (2015) Newborn screening for lysosomal storage diseases. Clin Chem 61:335–346CrossRefPubMed Gelb MH, Scott CR, Turecek F (2015) Newborn screening for lysosomal storage diseases. Clin Chem 61:335–346CrossRefPubMed
go back to reference Gucciardi A, Legini E, Di Gangi IM et al (2014) A column-switching HPLC-MS/MS method for mucopolysaccharidosis type I analysis in a multiplex assay for the simultaneous newborn screening of six lysosomal storage disorders. Biomed Chromatogr 28:1131–1139CrossRefPubMed Gucciardi A, Legini E, Di Gangi IM et al (2014) A column-switching HPLC-MS/MS method for mucopolysaccharidosis type I analysis in a multiplex assay for the simultaneous newborn screening of six lysosomal storage disorders. Biomed Chromatogr 28:1131–1139CrossRefPubMed
go back to reference Hennessey PT, Hurst RE, Hemstreet GP et al (1981) Urinary glycosaminoglycan excretion as a biochemical marker in patients with bladder carcinoma. Cancer Res 41:3868–3873PubMed Hennessey PT, Hurst RE, Hemstreet GP et al (1981) Urinary glycosaminoglycan excretion as a biochemical marker in patients with bladder carcinoma. Cancer Res 41:3868–3873PubMed
go back to reference Hopkins PV, Campbell C, Klug T et al (2015) Lysosomal storage disorder screening implementation: findings from the first six months of full population pilot testing in Missouri. J Pediatr 166:172–177CrossRefPubMed Hopkins PV, Campbell C, Klug T et al (2015) Lysosomal storage disorder screening implementation: findings from the first six months of full population pilot testing in Missouri. J Pediatr 166:172–177CrossRefPubMed
go back to reference Komosinska-Vassev K, Olczyk K, Kozma EM et al (2005) Alterations of glycosaminoglycan metabolism in the development of diabetic complications in relation to metabolic control. Clin Chem Lab Med 43:924–929CrossRefPubMed Komosinska-Vassev K, Olczyk K, Kozma EM et al (2005) Alterations of glycosaminoglycan metabolism in the development of diabetic complications in relation to metabolic control. Clin Chem Lab Med 43:924–929CrossRefPubMed
go back to reference Lawrence R, Brown JR, Al-Mafraji K et al (2012) Disease-specific non-reducing end carbohydrate biomarkers for mucopolysaccharidoses. Nat Chem Biol 8:197–204CrossRefPubMedPubMedCentral Lawrence R, Brown JR, Al-Mafraji K et al (2012) Disease-specific non-reducing end carbohydrate biomarkers for mucopolysaccharidoses. Nat Chem Biol 8:197–204CrossRefPubMedPubMedCentral
go back to reference Lawrence R, Brown JR, Lorey F et al (2014) Glycan-based biomarkers for mucopolysaccharidoses. Mol Genet Metab 111:73–83CrossRefPubMed Lawrence R, Brown JR, Lorey F et al (2014) Glycan-based biomarkers for mucopolysaccharidoses. Mol Genet Metab 111:73–83CrossRefPubMed
go back to reference Leys C, Ley C, Klein O et al (2013) Detecting outliers: do not use standard deviation around the mean, use absolute deviation around the median. J Exp Soc Psychol 49:764–766CrossRef Leys C, Ley C, Klein O et al (2013) Detecting outliers: do not use standard deviation around the mean, use absolute deviation around the median. J Exp Soc Psychol 49:764–766CrossRef
go back to reference Liao HC, Chiang CC, Niu DM et al (2014) Detecting multiple lysosomal storage diseases by tandem mass spectrometry—a national newborn screening program in Taiwan. Clin Chem Acta 431:80–86CrossRef Liao HC, Chiang CC, Niu DM et al (2014) Detecting multiple lysosomal storage diseases by tandem mass spectrometry—a national newborn screening program in Taiwan. Clin Chem Acta 431:80–86CrossRef
go back to reference Lin SP, Lin HY, Wang TJ et al (2013) A pilot newborn screening program for Mucopolysaccharidosis type I in Taiwan. Orphanet J Rare Dis 22:1–8 Lin SP, Lin HY, Wang TJ et al (2013) A pilot newborn screening program for Mucopolysaccharidosis type I in Taiwan. Orphanet J Rare Dis 22:1–8
go back to reference Martin JJ, Ceuterick C (1983) Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases. Clin Neuropathol 2:122–127PubMed Martin JJ, Ceuterick C (1983) Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases. Clin Neuropathol 2:122–127PubMed
go back to reference McGill JJ, Inwood AC, Coman DJ et al (2010) Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age—a sibling control study. Clin Genet 77:492–498CrossRefPubMed McGill JJ, Inwood AC, Coman DJ et al (2010) Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age—a sibling control study. Clin Genet 77:492–498CrossRefPubMed
go back to reference Meikle PJ, Grasby DJ, Dean CJ et al (2006) Newborn screening for lysosomal storage disorders. Mol Genet Metab 88:307–314CrossRefPubMed Meikle PJ, Grasby DJ, Dean CJ et al (2006) Newborn screening for lysosomal storage disorders. Mol Genet Metab 88:307–314CrossRefPubMed
go back to reference Muenzer J (2014) Early initiation of enzyme replacement therapy for the mucopolysaccharidoses. Mol Genet Metab 111:63–72CrossRefPubMed Muenzer J (2014) Early initiation of enzyme replacement therapy for the mucopolysaccharidoses. Mol Genet Metab 111:63–72CrossRefPubMed
go back to reference Neufeld E, Muenzer J (2001) The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease, 8th edn. McGraw-Hill, New York, pp 3421–3452 Neufeld E, Muenzer J (2001) The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease, 8th edn. McGraw-Hill, New York, pp 3421–3452
go back to reference Oguma T, Tomatsu S, Montaño AM et al (2007) Analytical method for determination of disaccharides derived from keratan, heparan, and dermatan sulfates in human serum and plasma by high-performance liquid chromatography/turbo ionspray ionization tandem mass spectrometry. Anal Biochem 368:79–86CrossRefPubMed Oguma T, Tomatsu S, Montaño AM et al (2007) Analytical method for determination of disaccharides derived from keratan, heparan, and dermatan sulfates in human serum and plasma by high-performance liquid chromatography/turbo ionspray ionization tandem mass spectrometry. Anal Biochem 368:79–86CrossRefPubMed
go back to reference Ohashi A, Montaño AM, Colón JE et al (2009) Sacral dimple: incidental findings from newborn evaluation. Mucopolysaccharidosis IVA disease. Acta Paediatr 98:768–769CrossRefPubMed Ohashi A, Montaño AM, Colón JE et al (2009) Sacral dimple: incidental findings from newborn evaluation. Mucopolysaccharidosis IVA disease. Acta Paediatr 98:768–769CrossRefPubMed
go back to reference Poe MD, Chagnon SL, Escolar ML (2014) Early treatment is associated with improved cognition in Hurler syndrome. Ann Neurol 76:1–24CrossRef Poe MD, Chagnon SL, Escolar ML (2014) Early treatment is associated with improved cognition in Hurler syndrome. Ann Neurol 76:1–24CrossRef
go back to reference Rowan DJ, Tomatsu S, Grubb JH et al (2013) Assessment of bone dysplasia by micro-CT and glycosaminoglycan levels in mouse models for mucopolysaccharidosis type I, IIA, IVA and VII. J Inherit Metab Dis 36:235–246CrossRefPubMed Rowan DJ, Tomatsu S, Grubb JH et al (2013) Assessment of bone dysplasia by micro-CT and glycosaminoglycan levels in mouse models for mucopolysaccharidosis type I, IIA, IVA and VII. J Inherit Metab Dis 36:235–246CrossRefPubMed
go back to reference Ruijter GJ, Goudriaan DA, Boer AM et al (2014) Newborn screening for hunter disease: a small-scale feasibility study. J Inherit Metab Dis Rep 14:23–27 Ruijter GJ, Goudriaan DA, Boer AM et al (2014) Newborn screening for hunter disease: a small-scale feasibility study. J Inherit Metab Dis Rep 14:23–27
go back to reference Saad OM, Ebel H, Uchimura K et al (2005) Compositional profiling of heparin/heparan sulfate using mass spectrometry: assay for specificity of a novel extracellular human endosulfatase. Glycobiology 15:818–826CrossRefPubMed Saad OM, Ebel H, Uchimura K et al (2005) Compositional profiling of heparin/heparan sulfate using mass spectrometry: assay for specificity of a novel extracellular human endosulfatase. Glycobiology 15:818–826CrossRefPubMed
go back to reference Schulze-Frenking G, Jones SA, Roberts J et al (2011) Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type II. J Inherit Metab Dis 34:203–208CrossRefPubMed Schulze-Frenking G, Jones SA, Roberts J et al (2011) Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type II. J Inherit Metab Dis 34:203–208CrossRefPubMed
go back to reference Scott CR, Elliott S, Buroker N et al (2013) Identification of infants at risk for developing Fabry, Pompe, or Mucopolysaccharidosis-I from newborn blood spots by tandem mass spectrometry. J Pediatr 163:498–503CrossRefPubMedPubMedCentral Scott CR, Elliott S, Buroker N et al (2013) Identification of infants at risk for developing Fabry, Pompe, or Mucopolysaccharidosis-I from newborn blood spots by tandem mass spectrometry. J Pediatr 163:498–503CrossRefPubMedPubMedCentral
go back to reference Shimada T, Kelly J, LaMarr WA et al (2014a) Novel heparan sulfate assay by using automated high-throughput mass spectrometry: application to monitoring and screening for mucopolysaccharidoses. Mol Genet Metab 113:92–99CrossRefPubMedPubMedCentral Shimada T, Kelly J, LaMarr WA et al (2014a) Novel heparan sulfate assay by using automated high-throughput mass spectrometry: application to monitoring and screening for mucopolysaccharidoses. Mol Genet Metab 113:92–99CrossRefPubMedPubMedCentral
go back to reference Shimada T, Tomatsu S, Yasuda E et al (2014b) Chondroitin 6-sulfate as a novel biomarker for mucopolysaccharidosis type I, IIIA, IVA and VII. J Inherit Metab Dis Rep 16:15–24 Shimada T, Tomatsu S, Yasuda E et al (2014b) Chondroitin 6-sulfate as a novel biomarker for mucopolysaccharidosis type I, IIIA, IVA and VII. J Inherit Metab Dis Rep 16:15–24
go back to reference Shimada T, Tomatsu S, Mason RW et al (2015) Di-sulfated KS as a novel biomarker for mucopolysaccharidosis II, IVA, and IVB. J Inherit Metab Dis Rep 21:1–13 Shimada T, Tomatsu S, Mason RW et al (2015) Di-sulfated KS as a novel biomarker for mucopolysaccharidosis II, IVA, and IVB. J Inherit Metab Dis Rep 21:1–13
go back to reference Tomatsu S, Orii KO, Vogler C et al (2003) Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns−/−) produced by targeted disruption of the gene defective in Morquio A Disease. Hum Mol Genet 12:3349–3358CrossRefPubMed Tomatsu S, Orii KO, Vogler C et al (2003) Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns−/−) produced by targeted disruption of the gene defective in Morquio A Disease. Hum Mol Genet 12:3349–3358CrossRefPubMed
go back to reference Tomatsu S, Okamura K, Maeda H et al (2005) Keratan sulphate levels in mucopolysaccharidoses and mucolipidoses. J Inherit Metab Dis 28:187–202CrossRefPubMed Tomatsu S, Okamura K, Maeda H et al (2005) Keratan sulphate levels in mucopolysaccharidoses and mucolipidoses. J Inherit Metab Dis 28:187–202CrossRefPubMed
go back to reference Tomatsu S, Montaño AM, Oguma T et al (2010) Validation of keratan sulfate level in mucopolysaccharidosis IVA by liquid tandem mass spectrometry method. J Inherit Metab Dis 33:35–42CrossRef Tomatsu S, Montaño AM, Oguma T et al (2010) Validation of keratan sulfate level in mucopolysaccharidosis IVA by liquid tandem mass spectrometry method. J Inherit Metab Dis 33:35–42CrossRef
go back to reference Tomatsu S, Almeciga-Diaz CJ, Montano AM et al (2015) Therapies for the bone in mucopolysaccharidoses. Mol Genet Metab 114:94–109CrossRefPubMed Tomatsu S, Almeciga-Diaz CJ, Montano AM et al (2015) Therapies for the bone in mucopolysaccharidoses. Mol Genet Metab 114:94–109CrossRefPubMed
go back to reference Tomatsu S, Azario I, Sawamoto K et al (2016) Neonatal cellular and gene therapies for mucopolysaccharidoses: the earlier the better? J Inherit Metab Dis 39:189–202CrossRefPubMed Tomatsu S, Azario I, Sawamoto K et al (2016) Neonatal cellular and gene therapies for mucopolysaccharidoses: the earlier the better? J Inherit Metab Dis 39:189–202CrossRefPubMed
go back to reference Turgeon CT, Magera MJ, Cuthbert CD et al (2010) Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry. Clin Chem 56:1686–1695CrossRefPubMed Turgeon CT, Magera MJ, Cuthbert CD et al (2010) Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry. Clin Chem 56:1686–1695CrossRefPubMed
go back to reference Vogler C, Birkenmeier EH, Sly WS et al (1990) A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice. Am J Pathol 136:207–217PubMedPubMedCentral Vogler C, Birkenmeier EH, Sly WS et al (1990) A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice. Am J Pathol 136:207–217PubMedPubMedCentral
go back to reference Wei W, Ninñonuevo MR, Sharma A et al (2011) A comprehensive compositional analysis of heparin/heparan sulfate-derived disaccharides from human serum. Anal Chem 83:3703–3708CrossRefPubMedPubMedCentral Wei W, Ninñonuevo MR, Sharma A et al (2011) A comprehensive compositional analysis of heparin/heparan sulfate-derived disaccharides from human serum. Anal Chem 83:3703–3708CrossRefPubMedPubMedCentral
go back to reference Wolfe BJ, Blanchard S, Sadilek M et al (2011) Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis II (Hunter syndrome). Anal Chem 83:1152–1156CrossRefPubMed Wolfe BJ, Blanchard S, Sadilek M et al (2011) Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis II (Hunter syndrome). Anal Chem 83:1152–1156CrossRefPubMed
go back to reference Zhang Y, Conrad AH, Tasheva ES et al (2005) Detection and quantification of sulfated disaccharides from keratin sulfate and chondroitin/dermatan sulfate during chick corneal development by ESI-MS/MS. Invest Ophthalmol Vis Sci 46:1604–1614CrossRefPubMed Zhang Y, Conrad AH, Tasheva ES et al (2005) Detection and quantification of sulfated disaccharides from keratin sulfate and chondroitin/dermatan sulfate during chick corneal development by ESI-MS/MS. Invest Ophthalmol Vis Sci 46:1604–1614CrossRefPubMed
Metadata
Title
Newborn screening for mucopolysaccharidoses: a pilot study of measurement of glycosaminoglycans by tandem mass spectrometry
Authors
Francyne Kubaski
Robert W. Mason
Akiko Nakatomi
Haruo Shintaku
Li Xie
Naomi N. van Vlies
Heather Church
Roberto Giugliani
Hironori Kobayashi
Seiji Yamaguchi
Yasuyuki Suzuki
Tadao Orii
Toshiyuki Fukao
Adriana M. Montaño
Shunji Tomatsu
Publication date
01-01-2017
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 1/2017
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-016-9981-6

Other articles of this Issue 1/2017

Journal of Inherited Metabolic Disease 1/2017 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine