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α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females

•The α-Gal A/lysoGb3 ratio is a promising marker of Fabry disease in females.•A correlation between lysoGb3 concentration and age was found.•LysoGb3 levels were different between asymptomatic/symptomatic FD female patients. Fabry disease (FD [MIM:301500]) is an X-linked lysosomal storage disorder ca...

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Published in:Clinica chimica acta 2020-02, Vol.501, p.27-32
Main Authors: Baydakova, G.V., Ilyushkina, A.A., Moiseev, S., Bychkov, I.O., Nikitina, N.V., Buruleva, Т.А., Zakharova, E.Y.
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cited_by cdi_FETCH-LOGICAL-c353t-c208cc402a44e82bd1386ec002f6346e4cd94fa68fd37851b8204e9a374e5aa63
cites cdi_FETCH-LOGICAL-c353t-c208cc402a44e82bd1386ec002f6346e4cd94fa68fd37851b8204e9a374e5aa63
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container_title Clinica chimica acta
container_volume 501
creator Baydakova, G.V.
Ilyushkina, A.A.
Moiseev, S.
Bychkov, I.O.
Nikitina, N.V.
Buruleva, Т.А.
Zakharova, E.Y.
description •The α-Gal A/lysoGb3 ratio is a promising marker of Fabry disease in females.•A correlation between lysoGb3 concentration and age was found.•LysoGb3 levels were different between asymptomatic/symptomatic FD female patients. Fabry disease (FD [MIM:301500]) is an X-linked lysosomal storage disorder caused by mutations in the GLA gene. Deficient activity of its product, lysosomal enzyme α-galactosidase A (α-Gal A), leads to excessive accumulation of glycosphingolipids in cells of multiple organs. The establishing of the diagnosis is challenge in female patients because of milder clinical manifestation and normal α-Gal A activity. The globotriaosylsphingosine (lysoGb3) is described as a more sensitive diagnostic biomarker for females with pathogenic mutation in the GLA gene. Thus, the aim of this study is to improve the biochemical diagnostic efficiency for FD in females. Here we report the α-Gal A/lysoGb3 ratio as the novel biochemical criteria for diagnosis of female patients with FD, using dried blood spots (DBS) as test samples. It showed 100% sensitivity in distinguishing our group of 35 female patients from control (n = 140). Whereas measurement of α-Gal A and lysoGb3 alone showed 8.6% and 74.4% respectively. A new approach of using the ratio of α-Gal A activity to lysoGb3 concentration in DBS may provide a more accurate screening tool for identification of FD females.
doi_str_mv 10.1016/j.cca.2019.10.031
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Fabry disease (FD [MIM:301500]) is an X-linked lysosomal storage disorder caused by mutations in the GLA gene. Deficient activity of its product, lysosomal enzyme α-galactosidase A (α-Gal A), leads to excessive accumulation of glycosphingolipids in cells of multiple organs. The establishing of the diagnosis is challenge in female patients because of milder clinical manifestation and normal α-Gal A activity. The globotriaosylsphingosine (lysoGb3) is described as a more sensitive diagnostic biomarker for females with pathogenic mutation in the GLA gene. Thus, the aim of this study is to improve the biochemical diagnostic efficiency for FD in females. Here we report the α-Gal A/lysoGb3 ratio as the novel biochemical criteria for diagnosis of female patients with FD, using dried blood spots (DBS) as test samples. It showed 100% sensitivity in distinguishing our group of 35 female patients from control (n = 140). Whereas measurement of α-Gal A and lysoGb3 alone showed 8.6% and 74.4% respectively. 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Fabry disease (FD [MIM:301500]) is an X-linked lysosomal storage disorder caused by mutations in the GLA gene. Deficient activity of its product, lysosomal enzyme α-galactosidase A (α-Gal A), leads to excessive accumulation of glycosphingolipids in cells of multiple organs. The establishing of the diagnosis is challenge in female patients because of milder clinical manifestation and normal α-Gal A activity. The globotriaosylsphingosine (lysoGb3) is described as a more sensitive diagnostic biomarker for females with pathogenic mutation in the GLA gene. Thus, the aim of this study is to improve the biochemical diagnostic efficiency for FD in females. Here we report the α-Gal A/lysoGb3 ratio as the novel biochemical criteria for diagnosis of female patients with FD, using dried blood spots (DBS) as test samples. It showed 100% sensitivity in distinguishing our group of 35 female patients from control (n = 140). Whereas measurement of α-Gal A and lysoGb3 alone showed 8.6% and 74.4% respectively. 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Fabry disease (FD [MIM:301500]) is an X-linked lysosomal storage disorder caused by mutations in the GLA gene. Deficient activity of its product, lysosomal enzyme α-galactosidase A (α-Gal A), leads to excessive accumulation of glycosphingolipids in cells of multiple organs. The establishing of the diagnosis is challenge in female patients because of milder clinical manifestation and normal α-Gal A activity. The globotriaosylsphingosine (lysoGb3) is described as a more sensitive diagnostic biomarker for females with pathogenic mutation in the GLA gene. Thus, the aim of this study is to improve the biochemical diagnostic efficiency for FD in females. Here we report the α-Gal A/lysoGb3 ratio as the novel biochemical criteria for diagnosis of female patients with FD, using dried blood spots (DBS) as test samples. It showed 100% sensitivity in distinguishing our group of 35 female patients from control (n = 140). Whereas measurement of α-Gal A and lysoGb3 alone showed 8.6% and 74.4% respectively. A new approach of using the ratio of α-Gal A activity to lysoGb3 concentration in DBS may provide a more accurate screening tool for identification of FD females.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31770509</pmid><doi>10.1016/j.cca.2019.10.031</doi><tpages>6</tpages></addata></record>
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ispartof Clinica chimica acta, 2020-02, Vol.501, p.27-32
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subjects Adolescent
Adult
Aged
alpha-Galactosidase - blood
alpha-Galactosidase - genetics
Biochemical markers
Biomarkers - blood
Child
Dried Blood Spot Testing
Fabry disease
Fabry Disease - blood
Fabry Disease - diagnosis
Female
Genotype
GLA gene
Globotriaosylsphingosine
Glycolipids - blood
Glycolipids - genetics
Humans
Inherited metabolic diseases
Lysosomal disorders
Middle Aged
Sphingolipids - blood
Sphingolipids - genetics
Young Adult
title α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females
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