Literature DB >> 29779903

Glycosaminoglycans analysis in blood and urine of patients with mucopolysaccharidosis.

Shaukat A Khan1, Robert W Mason1, Roberto Giugliani2, Kenji Orii3, Toshiyuki Fukao3, Yasuyuki Suzuki4, Seiji Yamaguchi5, Hironori Kobayashi5, Tadao Orii3, Shunji Tomatsu6.   

Abstract

To explore the correlation between glycosaminoglycan (GAG) levels and mucopolysaccharidosis (MPS) type, we have evaluated the GAG levels in blood of MPS II, III, IVA, and IVB and urine of MPS IVA, IVB, and VI by tandem mass spectrometry. Dermatan sulfate (DS), heparan sulfate (HS), keratan sulfate (KS; mono-sulfated KS, di-sulfated KS), and the ratio of di-sulfated KS in total KS were measured. Patients with untreated MPS II had higher levels of DS and HS in blood while untreated MPS III had higher levels of HS in blood than age-matched controls. Untreated MPS IVA had higher levels of KS in blood and urine than age-matched controls. The ratio of blood di-sulfated KS/total KS in untreated MPS IVA was constant and higher than that in controls for children up to 10 years of age. The ratio of urine di-sulfated KS/total KS in untreated MPS IVA was also higher than that in age-matched controls, but the ratio in untreated MPS IVB was lower than controls. ERT reduced blood DS and HS in MPS II, and urine KS in MPS IVA patients, although GAGs levels remained higher than the observed in age-matched controls. ERT did not change blood KS levels in MPS IVA. MPS VI under ERT still had an elevation of urine DS level compared to age-matched controls. There was a positive correlation between blood and urine KS in untreated MPS IVA patients but not in MPS IVA patients treated with ERT. Blood and urine KS levels were secondarily elevated in MPS II and VI, respectively. Overall, measurement of GAG levels in blood and urine is useful for diagnosis of MPS, while urine KS is not a useful biomarker for monitoring therapeutic efficacy in MPS IVA.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Chondroitin sulfate; Dermatan sulfate; Glycosaminoglycans; Heparan sulfate; Hyaluronan; Keratan sulfate; LC/MS; Mucopolysaccharidoses

Mesh:

Substances:

Year:  2018        PMID: 29779903      PMCID: PMC6175648          DOI: 10.1016/j.ymgme.2018.04.011

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  56 in total

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2.  The spot test is not a reliable screening procedure for mucopolysaccharidoses.

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Journal:  Clin Chem       Date:  1991-04       Impact factor: 8.327

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Authors:  Haoyue Zhang; Sarah P Young; Christiane Auray-Blais; Paul J Orchard; Jakub Tolar; David S Millington
Journal:  Clin Chem       Date:  2011-05-16       Impact factor: 8.327

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Journal:  J Chromatogr       Date:  1966-01

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Journal:  Anal Biochem       Date:  1998-02-15       Impact factor: 3.365

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Journal:  Anal Biochem       Date:  2001-03-01       Impact factor: 3.365

7.  Analytical method for determination of disaccharides derived from keratan sulfates in human serum and plasma by high-performance liquid chromatography/turbo-ionspray ionization tandem mass spectrometry.

Authors:  Toshihiro Oguma; Shunji Tomatsu; Osamu Okazaki
Journal:  Biomed Chromatogr       Date:  2007-04       Impact factor: 1.902

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Journal:  Anal Biochem       Date:  1984-08-01       Impact factor: 3.365

9.  Acidolysis-based component mapping of glycosaminoglycans by reversed-phase high-performance liquid chromatography with off-line electrospray ionization-tandem mass spectrometry: evidence and tags to distinguish different glycosaminoglycans.

Authors:  He Zhu; Xuan Chen; Xiao Zhang; Lili Liu; Dapeng Cong; Xia Zhao; Guangli Yu
Journal:  Anal Biochem       Date:  2014-07-30       Impact factor: 3.365

10.  Validation of keratan sulfate level in mucopolysaccharidosis type IVA by liquid chromatography-tandem mass spectrometry.

Authors:  Shunji Tomatsu; Adriana M Montaño; Toshihiro Oguma; Vu Chi Dung; Hirotaka Oikawa; Talita Giacomet de Carvalho; María L Gutiérrez; Seiji Yamaguchi; Yasuyuki Suzuki; Masaru Fukushi; Kazuhiro Kida; Mitsuru Kubota; Luis Barrera; Tadao Orii
Journal:  J Inherit Metab Dis       Date:  2010-01-27       Impact factor: 4.982

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  24 in total

Review 1.  Enzyme replacement therapy for mucopolysaccharidoses; past, present, and future.

Authors:  Hui Hsuan Chen; Kazuki Sawamoto; Robert W Mason; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Shunji Tomatsu
Journal:  J Hum Genet       Date:  2019-08-27       Impact factor: 3.172

2.  Effect of enzyme replacement therapy on the growth of patients with Morquio A.

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Journal:  J Hum Genet       Date:  2019-04-24       Impact factor: 3.172

Review 3.  Advances in glycosaminoglycan detection.

Authors:  Shaukat A Khan; Robert W Mason; Hironori Kobayashi; Seiji Yamaguchi; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2020-03-27       Impact factor: 4.797

Review 4.  Molecular genetics and metabolism, special edition: Diagnosis, diagnosis and prognosis of Mucopolysaccharidosis IVA.

Authors:  Hira Peracha; Kazuki Sawamoto; Lauren Averill; Heidi Kecskemethy; Mary Theroux; Mihir Thacker; Kyoko Nagao; Christian Pizarro; William Mackenzie; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Toshiyuki Fukao; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2018-05-15       Impact factor: 4.797

Review 5.  Therapeutic Options for Mucopolysaccharidoses: Current and Emerging Treatments.

Authors:  Kazuki Sawamoto; Molly Stapleton; Carlos J Alméciga-Díaz; Angela J Espejo-Mojica; Juan Camilo Losada; Diego A Suarez; Shunji Tomatsu
Journal:  Drugs       Date:  2019-07       Impact factor: 11.431

6.  Liver-Targeted AAV8 Gene Therapy Ameliorates Skeletal and Cardiovascular Pathology in a Mucopolysaccharidosis IVA Murine Model.

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Journal:  Mol Ther Methods Clin Dev       Date:  2020-05-22       Impact factor: 6.698

7.  Recommendations for the management of MPS IVA: systematic evidence- and consensus-based guidance.

Authors:  Mehmet Umut Akyol; Tord D Alden; Hernan Amartino; Jane Ashworth; Kumar Belani; Kenneth I Berger; Andrea Borgo; Elizabeth Braunlin; Yoshikatsu Eto; Jeffrey I Gold; Andrea Jester; Simon A Jones; Cengiz Karsli; William Mackenzie; Diane Ruschel Marinho; Andrew McFadyen; Jim McGill; John J Mitchell; Joseph Muenzer; Torayuki Okuyama; Paul J Orchard; Bob Stevens; Sophie Thomas; Robert Walker; Robert Wynn; Roberto Giugliani; Paul Harmatz; Christian Hendriksz; Maurizio Scarpa
Journal:  Orphanet J Rare Dis       Date:  2019-06-13       Impact factor: 4.123

8.  Morquio-B disease: Clinical and genetic characteristics of a distinct GLB1-related dysostosis multiplex.

Authors:  Iman S Abumansour; Nataliya Yuskiv; Eduard Paschke; Sylvia Stockler-Ipsiroglu
Journal:  JIMD Rep       Date:  2019-11-28

9.  Morquio-like dysostosis multiplex presenting with neuronopathic features is a distinct GLB1-related phenotype.

Authors:  Sylvia Stockler-Ipsiroglu; Nahid Yazdanpanah; Mojgan Yazdanpanah; Marioara Moisa Popurs; Nataliya Yuskiv; Mara Lúcia Schmitz Ferreira Santos; Chong Ae Kim; Carolina Fischinger Moura de Souza; Charles Marques Lourenço; Carlos Eduardo Steiner; Andressa Federhen; Luciana Giugliani; Débora Maria Bastos Pereira; Luz Elena Durán-Carabali; Roberto Giugliani
Journal:  JIMD Rep       Date:  2021-03-08

10.  In utero adenine base editing corrects multi-organ pathology in a lethal lysosomal storage disease.

Authors:  Sourav K Bose; Brandon M White; Meghana V Kashyap; Apeksha Dave; Felix R De Bie; Haiying Li; Kshitiz Singh; Pallavi Menon; Tiankun Wang; Shiva Teerdhala; Vishal Swaminathan; Heather A Hartman; Sowmya Jayachandran; Prashant Chandrasekaran; Kiran Musunuru; Rajan Jain; David B Frank; Philip Zoltick; William H Peranteau
Journal:  Nat Commun       Date:  2021-07-13       Impact factor: 14.919

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