La Marca, Giancarlo

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Florence Research

BACKGROUNDThe newborn screening (NBS) programme is a complex and organised system consisting of family and personal education, biochemical tests, confi rma-tory biochemical and genetic tests, diagnosis, therapy, and patient follow-up. The programme identifi es treatable metabolic disorders, possibly when still as-ymptomatic, by using dried blood spot (DBS). Over the last 20 years, tandem mass spectrometry (TMS) has become the leading technology in NBS pro-grammes and has been shown to be versatile, sensitive and specifi c. There is consistent evidence of benefi ts from NBS for many disorders detected by TMS as well as for congenital hypothyroidism, cystic fi brosis and congenital adrenal hyperplasia by immune-enzy-matic methods. Some methods were developed for the detection of lysosomal storage disorders (LSDs), and even if for some of them there is a reliable and rela-tively simple test, a reasonable associated therapy may still not be available. Therefore the inclusion of LSDs in NBS is still under debate.MATERIALS AND METHODSAt the beginning of the 2000’s, fl uorometric meth-ods were developed for many LSDs such as Pompe disease, Gaucher disease, Fabry disease, mucopoly-saccharidosis (MPS), Hurler-like LSDs, Niemann-Pick A/B disease, Tay-Sachs disease and Sandhoff disease. However, the incorporation of a chromophore or fl uorophore into the substrate caused false-negative results and had the limitations of specifi city and lim-ited capacity for multiplexing. In recent years new Newborn Screening: Are We Ready for It? Giancarlo la Marca*Clinical and Preclinical Pharmacology Department, University of Florence Mass Spectrometry, Clinical Chemistry and Pharmacology Labs, Meyer Children Hospital, Florence, ItalyJournal of Neuromuscular Diseases 1 (2015) S10DOI 10.3233/JND-159010IOS PressPlenary AbstractISSN 2214-3599/15/$27.50 © 2015 – IOS Press and the authors. All rights reservedThis article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License.MS-based technology for simultaneous screening of several enzyme activities related to lysosomal storage disorders from DBS was developed, replacing the old methods and enabling the assay of single enzyme ac-tivity. Li et al (1) fi rst developed a direct multiplex assay of lysosomal enzymes for Gaucher, Pompe, Krabbe, Fabry and Niemann-Pick A/B diseases in DBS by fl ow injection analysis (FIA) tandem mass spectrometry. Since then, an expansion of simultane-ously diagnosable disorders by MS has been reported. Some countries already include some LSDs in their newborn screening panels, and local or pilot pro-grammes have been launched in others. (2-6). CONCLUSIONSIt is currently debated whether or not LSD diseases should be included in a general NBS worldwide pro-gramme. In 2014, most LDS pilot projects include Pompe disease. In general, NBS for LSD could iden-tify asymptomatic forms; it is not able to discriminate between treatable and untreatable forms, surely it can-not suggest if and when to start therapy. However, even if long-term clinical studies are not available, it seems that Pompe disease meets the criteria for inclu-sion in NBS, including basal availability of a simple test, a combination therapy that modifi es the natural course of the disease, and early diagnosis that allows for genetic counsel ling and prenatal diagnosis in fam-ilies with an affected baby.REFERENCES[1]  Li et al; Clin Chem 2004, 50:1785-1796.[2]  Chien et al.; Pediatrics 2008, 122: doi: 10.1542/peds.2007-2222.[3]  Wittmann et al.; JIMD Rep 2012, 6:117-125.[4]  Paciotti et al.; Clin Chim Acta, 2012 413:1827-1831.[5]  Inoue et al.; Hum Genet 2013, 58:548-552.[6]  Liao et al.; 2014 Clin Chim Acta 2014, 431:80-86. *Correspondence to: Giancarlo la Marca, Dept of Neurosciences, Psychology, Pharmacology and Child Health, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy, Tel.: +39 055 5662988; Fax: +39 055 5662489. E-mail: g.lamarca@meyer.it; giancarlo.lamarca@unifi .it.

Newborn Screening: Are We Ready for It?

https://flore.unifi.it/bitstream/2158/1069887/1/PompeJND2015.pdf

Newborn Screening: Are We Ready for It?

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