Literature DB >> 23609959

Selective screening for lysosomal storage diseases with dried blood spots collected on filter paper in 4,700 high-risk colombian subjects.

Alfredo Uribe1, Roberto Giugliani.   

Abstract

Lysosomal storage disorders (LSDs) are a very heterogeneous group of hereditary disorders. The diagnostic process usually involves complex sampling, processing, testing, and validation procedures, performed by specialized laboratories only, which causes great limitations in reaching a diagnosis for patients affected by these diseases.There are few studies about LSDs in Colombia. The diagnostic limitations often make medical practitioners disregard the possibility of these disorders while diagnosing their patients. The current study documents the results of a 7-year screening in high-risk patients, aimed to detect LSDs using dried blood spots (DBS) collected on filter paper, with a micromethodology that facilitates diagnosis even with a large number of samples.The activities of α-galactosidase A, α glucosidase, α-L-iduronidase, arylsulfatase B, β-galactosidase, β-glucosidase, total hexosaminidase, iduronate sulfatase, and chitotriosidase were analyzed in high-risk patients for lysosomal disease. The catalytic activity was evaluated with fluorometric micromethods using artificial substrates marked with 4-methylumbelliferone.The reference values for a control population were established for the enzymes listed above, and 242 patients were found to have an enzyme deficiency, guiding to the following diagnoses: Fabry disease (n = 31), Pompe disease (n = 16), Hurler Syndrome (n = 15), Maroteaux-Lamy Syndrome (n = 34), GM1 Gangliosidosis (n = 10), Morquio B (n = 1), Gaucher disease (n = 101), Sandhoff disease (n = 1), Mucolipidosis (n = 2), and Hunter Syndrome (n = 31). In conclusion, this protocol provides a comprehensive diagnostic approach which could be carried out in Colombia and made it available to medical services spread around the country, enabling the identification of a large number of patients affected by LSDs, which could potentially benefit from the therapeutic tools already available for many of these diseases.

Entities:  

Year:  2013        PMID: 23609959      PMCID: PMC3755556          DOI: 10.1007/8904_2013_229

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  32 in total

1.  Hurler-like phenotype: enzymatic diagnosis in dried blood spots on filter paper.

Authors:  N A Chamoles; M B Blanco; D Gaggioli; C Casentini
Journal:  Clin Chem       Date:  2001-12       Impact factor: 8.327

2.  Fabry disease: enzymatic diagnosis in dried blood spots on filter paper.

Authors:  N A Chamoles; M Blanco; D Gaggioli
Journal:  Clin Chim Acta       Date:  2001-06       Impact factor: 3.786

Review 3.  Lysosomal disorders.

Authors:  J E Wraith
Journal:  Semin Neonatol       Date:  2002-02

Review 4.  The cell biology of lysosomal storage disorders.

Authors:  Anthony H Futerman; Gerrit van Meer
Journal:  Nat Rev Mol Cell Biol       Date:  2004-07       Impact factor: 94.444

5.  Twelve different enzyme assays on dried-blood filter paper samples for detection of patients with selected inherited lysosomal storage diseases.

Authors:  Gabriel Civallero; Kristiane Michelin; Jurema de Mari; Marli Viapiana; Maira Burin; Janice C Coelho; Roberto Giugliani
Journal:  Clin Chim Acta       Date:  2006-05-18       Impact factor: 3.786

6.  Measurements of arylsulfatases A and B in human serum.

Authors:  J Singh; D Tavella; N D Ferrante
Journal:  J Pediatr       Date:  1975-04       Impact factor: 4.406

7.  Hemoglobin precipitation greatly improves 4-methylumbelliferone-based diagnostic assays for lysosomal storage diseases in dried blood spots.

Authors:  L F Oemardien; A M Boer; G J G Ruijter; A T van der Ploeg; J B C de Klerk; A J J Reuser; F W Verheijen
Journal:  Mol Genet Metab       Date:  2010-09-26       Impact factor: 4.797

8.  A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease).

Authors:  Y V Voznyi; J L Keulemans; O P van Diggelen
Journal:  J Inherit Metab Dis       Date:  2001-11       Impact factor: 4.982

9.  The quantitative measurement of Alcian Blue-glycosaminoglycan complexes.

Authors:  P Whiteman
Journal:  Biochem J       Date:  1973-02       Impact factor: 3.857

Review 10.  Lysosomal storage disorders: diagnostic dilemmas and prospects for therapy.

Authors:  David A Wenger; Stephanie Coppola; Shu-Ling Liu
Journal:  Genet Med       Date:  2002 Nov-Dec       Impact factor: 8.822

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  3 in total

Review 1.  Pompe disease: literature review and case series.

Authors:  Majed Dasouki; Omar Jawdat; Osama Almadhoun; Mamatha Pasnoor; April L McVey; Ahmad Abuzinadah; Laura Herbelin; Richard J Barohn; Mazen M Dimachkie
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

2.  Lentivector Iterations and Pre-Clinical Scale-Up/Toxicity Testing: Targeting Mobilized CD34+ Cells for Correction of Fabry Disease.

Authors:  Ju Huang; Aneal Khan; Bryan C Au; Dwayne L Barber; Lucía López-Vásquez; Nicole L Prokopishyn; Michel Boutin; Michael Rothe; Jack W Rip; Mona Abaoui; Murtaza S Nagree; Shaalee Dworski; Axel Schambach; Armand Keating; Michael L West; John Klassen; Patricia V Turner; Sandra Sirrs; C Anthony Rupar; Christiane Auray-Blais; Ronan Foley; Jeffrey A Medin
Journal:  Mol Ther Methods Clin Dev       Date:  2017-05-12       Impact factor: 6.698

3.  Twenty years of Colombian experience with enzymatic screening in patients with features of mucopolysaccharidosis.

Authors:  Alfredo Uribe-Ardila; Johana Ramirez-Borda; Adis Ayala
Journal:  JIMD Rep       Date:  2022-07-28
  3 in total

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