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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 |
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container_title | Clinica chimica acta |
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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.
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.</description><identifier>ISSN: 0009-8981</identifier><identifier>EISSN: 1873-3492</identifier><identifier>DOI: 10.1016/j.cca.2019.10.031</identifier><identifier>PMID: 31770509</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>Clinica chimica acta, 2020-02, Vol.501, p.27-32</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-c208cc402a44e82bd1386ec002f6346e4cd94fa68fd37851b8204e9a374e5aa63</citedby><cites>FETCH-LOGICAL-c353t-c208cc402a44e82bd1386ec002f6346e4cd94fa68fd37851b8204e9a374e5aa63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31770509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baydakova, G.V.</creatorcontrib><creatorcontrib>Ilyushkina, A.A.</creatorcontrib><creatorcontrib>Moiseev, S.</creatorcontrib><creatorcontrib>Bychkov, I.O.</creatorcontrib><creatorcontrib>Nikitina, N.V.</creatorcontrib><creatorcontrib>Buruleva, Т.А.</creatorcontrib><creatorcontrib>Zakharova, E.Y.</creatorcontrib><title>α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females</title><title>Clinica chimica acta</title><addtitle>Clin Chim Acta</addtitle><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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>alpha-Galactosidase - blood</subject><subject>alpha-Galactosidase - genetics</subject><subject>Biochemical markers</subject><subject>Biomarkers - blood</subject><subject>Child</subject><subject>Dried Blood Spot Testing</subject><subject>Fabry disease</subject><subject>Fabry Disease - blood</subject><subject>Fabry Disease - diagnosis</subject><subject>Female</subject><subject>Genotype</subject><subject>GLA gene</subject><subject>Globotriaosylsphingosine</subject><subject>Glycolipids - blood</subject><subject>Glycolipids - genetics</subject><subject>Humans</subject><subject>Inherited metabolic diseases</subject><subject>Lysosomal disorders</subject><subject>Middle Aged</subject><subject>Sphingolipids - blood</subject><subject>Sphingolipids - genetics</subject><subject>Young Adult</subject><issn>0009-8981</issn><issn>1873-3492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kMFqGzEURUVpaZykH5BN0LKbsZ9GskaiKxNiJxDoIs1avNG8Abljy5XGBX9WfyTfVA1Ou8zqcR_3XriHsRsBcwFCL7Zz73Feg7BFz0GKD2wmTCMrqWz9kc0AwFbGGnHBLnPeFqlAi8_sQoqmgSXYGXt-_VNtcEA_xhw6zMRXi-GU46aVPOEYIsfMkR_iSPsx4MB3mH5S4n1MfI1tOvEuZJpyYc972uFA-Zp96nHI9OXtXrGX9f2Pu4fq6fvm8W71VHm5lGPlazDeK6hRKTJ12wlpNHmAutdSaVK-s6pHbfpONmYpWlODIouyUbRE1PKKfT33HlL8daQ8ul3InoYB9xSP2dVSWGGt1lCs4mz1KeacqHeHFMqUkxPgJpZu6wpLN7GcXoVlydy-1R_bHXX_E__gFcO3s4HKyN-Bkss-0N5TFxL50XUxvFP_F8R1g7M</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Baydakova, G.V.</creator><creator>Ilyushkina, A.A.</creator><creator>Moiseev, S.</creator><creator>Bychkov, I.O.</creator><creator>Nikitina, N.V.</creator><creator>Buruleva, Т.А.</creator><creator>Zakharova, E.Y.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202002</creationdate><title>α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females</title><author>Baydakova, G.V. ; Ilyushkina, A.A. ; Moiseev, S. ; Bychkov, I.O. ; Nikitina, N.V. ; Buruleva, Т.А. ; Zakharova, E.Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-c208cc402a44e82bd1386ec002f6346e4cd94fa68fd37851b8204e9a374e5aa63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>alpha-Galactosidase - blood</topic><topic>alpha-Galactosidase - genetics</topic><topic>Biochemical markers</topic><topic>Biomarkers - blood</topic><topic>Child</topic><topic>Dried Blood Spot Testing</topic><topic>Fabry disease</topic><topic>Fabry Disease - blood</topic><topic>Fabry Disease - diagnosis</topic><topic>Female</topic><topic>Genotype</topic><topic>GLA gene</topic><topic>Globotriaosylsphingosine</topic><topic>Glycolipids - blood</topic><topic>Glycolipids - genetics</topic><topic>Humans</topic><topic>Inherited metabolic diseases</topic><topic>Lysosomal disorders</topic><topic>Middle Aged</topic><topic>Sphingolipids - blood</topic><topic>Sphingolipids - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baydakova, G.V.</creatorcontrib><creatorcontrib>Ilyushkina, A.A.</creatorcontrib><creatorcontrib>Moiseev, S.</creatorcontrib><creatorcontrib>Bychkov, I.O.</creatorcontrib><creatorcontrib>Nikitina, N.V.</creatorcontrib><creatorcontrib>Buruleva, Т.А.</creatorcontrib><creatorcontrib>Zakharova, E.Y.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baydakova, G.V.</au><au>Ilyushkina, A.A.</au><au>Moiseev, S.</au><au>Bychkov, I.O.</au><au>Nikitina, N.V.</au><au>Buruleva, Т.А.</au><au>Zakharova, E.Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females</atitle><jtitle>Clinica chimica acta</jtitle><addtitle>Clin Chim Acta</addtitle><date>2020-02</date><risdate>2020</risdate><volume>501</volume><spage>27</spage><epage>32</epage><pages>27-32</pages><issn>0009-8981</issn><eissn>1873-3492</eissn><abstract>•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.</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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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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