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Published in: Clinical and Experimental Nephrology 4/2018

Open Access 01-08-2018 | Original article

Plasma lyso-Gb3: a biomarker for monitoring fabry patients during enzyme replacement therapy

Authors: Hitoshi Sakuraba, Tadayasu Togawa, Takahiro Tsukimura, Hiroshi Kato

Published in: Clinical and Experimental Nephrology | Issue 4/2018

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Abstract

Background

Recently, globotriaosylsphingosine (lyso-Gb3) has attracted interest as a biomarker of Fabry disease. However, little is known regarding its utility for the evaluation of the therapeutic efficacy.

Method

We measured plasma lyso-Gb3 concentration in Japanese healthy subjects and Fabry patients by means of liquid chromatography–tandem mass spectrometry (LC–MS/MS). We determined the reference interval in Japanese (UMIN000016854), and examined the effect of enzyme replacement therapy (ERT) with recombinant α-galactosidase A (GLA) and the influence of antibodies against the enzyme on the plasma lyso-Gb3 level in Fabry patients (UMIN000017152).

Results

The reference interval was determined to be 0.35–0.71 nmol/L, this being almost the same as the normal range in a non-Japanese population previously reported. The analysis revealed that the plasma lyso-Gb3 level was strikingly increased in classic Fabry males, and to a lesser extent in later-onset Fabry males and Fabry females. The elevation of the plasma lyso-Gb3 level was related to renal involvement in the Fabry females. ERT gave a rapid reduction in the elevated plasma lyso-Gb3 level in the classic Fabry males, and a gradual one or stabilization in most of the later-onset Fabry males and Fabry females. However, formation of antibodies against the recombinant GLA had a negative effect on the reduction of plasma lyso-Gb3.

Conclusions

Regular observation of plasma lyso-Gb3 and antibodies is useful for monitoring of Fabry patients during ERT.
Literature
2.
go back to reference Cox TM. Biomarkers in lysosomal storage disease. In: Mehta A, Beck M, Sunder Plassman G, editors. Fabry disease: perspective from 5 years of FOS. Oxford: Oxford PharmaGenesis. 2006;pp. 75–91. Cox TM. Biomarkers in lysosomal storage disease. In: Mehta A, Beck M, Sunder Plassman G, editors. Fabry disease: perspective from 5 years of FOS. Oxford: Oxford PharmaGenesis. 2006;pp. 75–91.
3.
go back to reference Aerts JM, Groener JE, Kuiper S, Donker-Koopman WE, Strijland A, Ottenhoff R, et al. Elevated globotriaosylsphingosine is a hallmark of Fabry disease. Proc Natl Acad Sci USA. 2008;105:2812–7.CrossRefPubMed Aerts JM, Groener JE, Kuiper S, Donker-Koopman WE, Strijland A, Ottenhoff R, et al. Elevated globotriaosylsphingosine is a hallmark of Fabry disease. Proc Natl Acad Sci USA. 2008;105:2812–7.CrossRefPubMed
4.
go back to reference Rombach SM, Dekker N, Bouwman MG, Linthorst GE, Zwinderman AH, Wijburg FA, et al. Plasma globotriaosylsphingosine: diagnostic value and relation to clinical manifestations of Fabry disease. Biochim Biophys Acta. 2010;1802:741–8.CrossRefPubMed Rombach SM, Dekker N, Bouwman MG, Linthorst GE, Zwinderman AH, Wijburg FA, et al. Plasma globotriaosylsphingosine: diagnostic value and relation to clinical manifestations of Fabry disease. Biochim Biophys Acta. 2010;1802:741–8.CrossRefPubMed
5.
go back to reference Togawa T, Kodama T, Suzuki T, Sugawara K, Tsukimura T, Ohashi T, et al. Plasma globotriaosylsphingosine as a biomarker of Fabry disease. Mol Genet Metab. 2010;100:257 – 61.CrossRefPubMed Togawa T, Kodama T, Suzuki T, Sugawara K, Tsukimura T, Ohashi T, et al. Plasma globotriaosylsphingosine as a biomarker of Fabry disease. Mol Genet Metab. 2010;100:257 – 61.CrossRefPubMed
6.
go back to reference Sueoka H, Ichihara J, Tsukimura T, Togawa T, Sakuraba H. Nano-LC–MS/MS for quantification of lyso-Gb3 and its analogues reveals a useful biomarker for Fabry disease. PLoS One. 2015;10:e0127048.CrossRefPubMedPubMedCentral Sueoka H, Ichihara J, Tsukimura T, Togawa T, Sakuraba H. Nano-LC–MS/MS for quantification of lyso-Gb3 and its analogues reveals a useful biomarker for Fabry disease. PLoS One. 2015;10:e0127048.CrossRefPubMedPubMedCentral
7.
go back to reference Schiffmann R, Kopp JB, Austin HA 3rd, Sabnis S, Moore DF, Weibei T, et al. Enzyme replacement therapy in Fabry disease: a randamized controlled trial. JAMA. 2001;285:2743–9.CrossRefPubMed Schiffmann R, Kopp JB, Austin HA 3rd, Sabnis S, Moore DF, Weibei T, et al. Enzyme replacement therapy in Fabry disease: a randamized controlled trial. JAMA. 2001;285:2743–9.CrossRefPubMed
8.
go back to reference van Breemen MJ, Rombach SM, Dekker N, Poorthuis BJ, Linthorst GE, Zwinderman AH, et al. Reduction of elevated plasma globotriaosylsphingosine in patients with classic Fabry disease following enzyme replacement therapy. Biochim Biophys Acta. 2011;1812:70 – 6.CrossRefPubMed van Breemen MJ, Rombach SM, Dekker N, Poorthuis BJ, Linthorst GE, Zwinderman AH, et al. Reduction of elevated plasma globotriaosylsphingosine in patients with classic Fabry disease following enzyme replacement therapy. Biochim Biophys Acta. 2011;1812:70 – 6.CrossRefPubMed
9.
go back to reference Lenders M, Stypmann J, Duning T, Schmitz B, Brand SM, Brand E. Serum-mediated inhibition of enzyme replacement therapy in Fabry disease. J Am Soc Nephrol. 2016;27:256 – 64.CrossRefPubMed Lenders M, Stypmann J, Duning T, Schmitz B, Brand SM, Brand E. Serum-mediated inhibition of enzyme replacement therapy in Fabry disease. J Am Soc Nephrol. 2016;27:256 – 64.CrossRefPubMed
10.
go back to reference Rombach SM, Aerts JM, Poorthuis BJ, Groener JE, Donker-Koopman W, Hendriks E, et al. Long-term effect of antibodies against infused alpha-galactosidase A in Fabry disease on plasma and urinary (lyso)Gb3 reduction and treatment outcome. PLoS One. 2012;7:e47805.CrossRefPubMedPubMedCentral Rombach SM, Aerts JM, Poorthuis BJ, Groener JE, Donker-Koopman W, Hendriks E, et al. Long-term effect of antibodies against infused alpha-galactosidase A in Fabry disease on plasma and urinary (lyso)Gb3 reduction and treatment outcome. PLoS One. 2012;7:e47805.CrossRefPubMedPubMedCentral
11.
go back to reference Gold H, Mirzaian M, Dekker N, Ferraz MJ, Lugtenburg J, Codée JDC, et al. Quantification of globotriaosylsphingosine in plasma and urine of Fabry patients by stable isotope ultraperformance liquid chromatography-tandem mass spectrometry. Clin Chem. 2013;59:547 – 56.CrossRefPubMed Gold H, Mirzaian M, Dekker N, Ferraz MJ, Lugtenburg J, Codée JDC, et al. Quantification of globotriaosylsphingosine in plasma and urine of Fabry patients by stable isotope ultraperformance liquid chromatography-tandem mass spectrometry. Clin Chem. 2013;59:547 – 56.CrossRefPubMed
12.
go back to reference Sanchez-Niño MD, Sanz AB, Carrasco S, Saleem MA, Mathieson PW, Valdivielso JM, et al. Globotriaosylsphingosine actions on human glomerular podocytes: implications for Fabry nephropathy. Nephrol Dial Transplant. 2011;26:1797 – 802.CrossRefPubMed Sanchez-Niño MD, Sanz AB, Carrasco S, Saleem MA, Mathieson PW, Valdivielso JM, et al. Globotriaosylsphingosine actions on human glomerular podocytes: implications for Fabry nephropathy. Nephrol Dial Transplant. 2011;26:1797 – 802.CrossRefPubMed
13.
go back to reference Deegan PB. Fabry disease, enzyme replacement therapy and the significance of antibody responses. J Inherit Metab Dis. 2012;35:227 – 43.CrossRefPubMed Deegan PB. Fabry disease, enzyme replacement therapy and the significance of antibody responses. J Inherit Metab Dis. 2012;35:227 – 43.CrossRefPubMed
14.
go back to reference Nakano S, Tsukimura T, Togawa T, Ohashi T, Kobayashi M, Takayama K, et al. Rapid immunochromatographic detection of serum anti-α-galactosidase A antibodies in Fabry patients after enzyme replacement therapy. PLoS One. 2015;10:e0128351.CrossRefPubMedPubMedCentral Nakano S, Tsukimura T, Togawa T, Ohashi T, Kobayashi M, Takayama K, et al. Rapid immunochromatographic detection of serum anti-α-galactosidase A antibodies in Fabry patients after enzyme replacement therapy. PLoS One. 2015;10:e0128351.CrossRefPubMedPubMedCentral
Metadata
Title
Plasma lyso-Gb3: a biomarker for monitoring fabry patients during enzyme replacement therapy
Authors
Hitoshi Sakuraba
Tadayasu Togawa
Takahiro Tsukimura
Hiroshi Kato
Publication date
01-08-2018
Publisher
Springer Singapore
Published in
Clinical and Experimental Nephrology / Issue 4/2018
Print ISSN: 1342-1751
Electronic ISSN: 1437-7799
DOI
https://doi.org/10.1007/s10157-017-1525-3

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