Reliable detection of mucopolysacchariduria in dried-urine filter paper samples

被引:17
作者
Civallero, G. [1 ,3 ]
Bender, F. [1 ]
Gomes, A. [1 ]
Marasca, G. [1 ]
Guidobono, R. [1 ]
De Mari, J. [1 ]
Burin, M. [1 ]
Giugliani, R. [1 ,2 ,3 ]
机构
[1] HCPA, Med Genet Serv, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Dept Genet, Porto Alegre, RS, Brazil
[3] INAGEMP, Porto Alegre, RS, Brazil
关键词
Inborn errors of metabolism; Lysosomal storage diseases; Mucopolysaccharidoses; Glycosaminoglycans; Screening; GLYCOSAMINOGLYCAN;
D O I
10.1016/j.cca.2012.11.009
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The mucopolysaccharidoses (MPS) are inherited metabolic disorders with bone, joint, and visceral abnormalities, leading to multi-organ dysfunction and, sometimes, neurological manifestations. These diseases are caused by storage of glycosaminoglycans (GAGS) and other complex molecules in tissues, among other pathogenic mechanisms. Definitive diagnosis of the affected individual is mainly based on the identification of the specific enzyme deficiency. New therapies are available or are in development for these pathologies, and early diagnosis seems to be important for the therapy outcomes. Almost all MPS patients have increased levels of GAGs in urine being their evaluation usually the first step in the screening of these conditions. Test on urine may be challenging as transportation of liquid urine samples in appropriate conditions for long distances, especially across international borders, could be difficult. Methods: With the aim of overcoming the difficulties related to the use of liquid samples, we extended and validated previous studies about colorimetric determination of GAGs in dried-urine filter paper (DUFF) samples. Results: In the conditions we described, there are no differences in the concentration of GAGs between urine and DUFP samples. Untreated patients with MPS and normal controls were well discriminated using any of the samples. Conclusions: Dried-urine filter paper is a suitable sample for the colorimetric quantitation of GAGs, and that its incorporation as an additional tool for screening of MPS should be considered by reference laboratories. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:334 / 336
页数:3
相关论文
共 8 条
[1]   Neonatal Screening for Mucopolysaccharidoses by Determination of Glycosaminoglycans in the Eluate of Urine-Impregnated Paper: Preliminary Results of an Improved DMB-Based Procedure [J].
Alonso-Fernandez, J. R. ;
Fidalgo, J. ;
Colon, C. .
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2010, 24 (03) :149-153
[2]   An improved method for glycosaminoglycan analysis by LC-MS/MS of urine samples collected on filter paper [J].
Auray-Blais, Christiane ;
Lavoie, Pamela ;
Zhang, Haoyue ;
Gagnon, Rene ;
Clarke, Joe T. R. ;
Maranda, Bruno ;
Young, Sarah P. ;
An, Yan ;
Millington, David S. .
CLINICA CHIMICA ACTA, 2012, 413 (7-8) :771-778
[3]  
Chamoles NA, 2001, CLIN CHEM, V47, P2098
[4]   Twelve different enzyme assays on dried-blood filter paper samples for detection of patients with selected inherited lysosomal storage diseases [J].
Civallero, Gabriel ;
Michelin, Kristiane ;
de Mari, Jurema ;
Viapiana, Marli ;
Burin, Maira ;
Coelho, Janice C. ;
Giugliani, Roberto .
CLINICA CHIMICA ACTA, 2006, 372 (1-2) :98-102
[5]  
DEJONG JGN, 1992, CLIN CHEM, V38, P803
[6]  
Valle D SO., 2001, METABOLIC MOL BASIS, P1909
[7]  
WHITLEY CB, 1989, CLIN CHEM, V35, P2074
[8]   Urinary glycosaminoglycan excretion quantified by an automated semimicro method in specimens conveniently transported from around the globe [J].
Whitley, CB ;
Spielmann, RC ;
Herro, G ;
Teragawa, SS .
MOLECULAR GENETICS AND METABOLISM, 2002, 75 (01) :56-64