Literature DB >> 19533645

Screening for Pompe disease using a rapid dried blood spot method: experience of a clinical diagnostic laboratory.

Jennifer L Goldstein1, Sarah P Young, Mohita Changela, Gwen H Dickerson, Haoyue Zhang, Jian Dai, Denise Peterson, David S Millington, Priya S Kishnani, Deeksha S Bali.   

Abstract

Pompe disease (acid maltase deficiency; glycogen storage disease type II) is caused by deficiency of the lysosomal enzyme acid alpha-glucosidase (GAA). Our clinical laboratory began to offer a fluorometric dried blood spot (DBS)-based GAA activity assay for Pompe disease in 2006 after the FDA approved GAA enzyme replacement therapy in April of that year. The purpose of this study was to examine the experience of our clinical laboratory in using this assay. Over a 2-year period, we received samples for the DBS GAA assay from 891 patients referred for possible Pompe disease, of whom 111 (12.5%) patients across the disease spectrum who had results in the affected range. The majority of the patients were referred by neurologists and geneticists. When available, we correlated the results obtained through DBS GAA activity assay with the results from a second DBS, or a second tissue (cultured skin fibroblasts or muscle biopsy). In our experience, the DBS GAA activity assay provides a robust, rapid, and reliable first tier test for screening patients suspected of having Pompe disease.

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Year:  2009        PMID: 19533645     DOI: 10.1002/mus.21376

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  11 in total

1.  Liquid Chromatography-Tandem Mass Spectrometry Assay of Leukocyte Acid α-Glucosidase for Post-Newborn Screening Evaluation of Pompe Disease.

Authors:  Na Lin; Jingyu Huang; Sara Violante; Joseph J Orsini; Michele Caggana; Erin E Hughes; Colleen Stevens; Lisa DiAntonio; Hsuan Chieh Liao; Xinying Hong; Farideh Ghomashchi; Arun Babu Kumar; Hui Zhou; Ruth Kornreich; Melissa Wasserstein; Michael H Gelb; Chunli Yu
Journal:  Clin Chem       Date:  2017-02-14       Impact factor: 8.327

2.  Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness.

Authors:  Zoltan Lukacs; Paulina Nieves Cobos; Stephan Wenninger; Tracey A Willis; Michela Guglieri; Marc Roberts; Rosaline Quinlivan; David Hilton-Jones; Teresinha Evangelista; Stephan Zierz; Beate Schlotter-Weigel; Maggie C Walter; Peter Reilich; Thomas Klopstock; Marcus Deschauer; Volker Straub; Wolfgang Müller-Felber; Benedikt Schoser
Journal:  Neurology       Date:  2016-05-11       Impact factor: 9.910

3.  Swiss national guideline for reimbursement of enzyme replacement therapy in late-onset Pompe disease.

Authors:  Thomas Hundsberger; Marianne Rohrbach; Lukas Kern; Kai M Rösler
Journal:  J Neurol       Date:  2013-06-08       Impact factor: 4.849

4.  Phenotypic implications of pathogenic variant types in Pompe disease.

Authors:  Manuel A Viamonte; Stephanie L Filipp; Zara Zaidi; Matthew J Gurka; Barry J Byrne; Peter B Kang
Journal:  J Hum Genet       Date:  2021-05-11       Impact factor: 3.172

Review 5.  Diagnosis of muscle diseases presenting with early respiratory failure.

Authors:  Gerald Pfeffer; Marcus Povitz; G John Gibson; Patrick F Chinnery
Journal:  J Neurol       Date:  2014-11-07       Impact factor: 4.849

6.  Clinical features of Pompe disease.

Authors:  Fiore Manganelli; Lucia Ruggiero
Journal:  Acta Myol       Date:  2013-10

7.  Highlighting intrafamilial clinical heterogeneity in late-onset Pompe disease.

Authors:  C Papadopoulos; G K Papadimas; H Michelakakis; E Kararizou; P Manta
Journal:  Mol Genet Metab Rep       Date:  2013-12-28

8.  Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship.

Authors:  Simone Sampaolo; Teresa Esposito; Olimpia Farina; Daniela Formicola; Daria Diodato; Fernando Gianfrancesco; Federica Cipullo; Gaetana Cremone; Mario Cirillo; Luca Del Viscovo; Antonio Toscano; Corrado Angelini; Giuseppe Di Iorio
Journal:  Orphanet J Rare Dis       Date:  2013-10-10       Impact factor: 4.123

9.  Evaluation prevalence of Pompe disease in Iranian patients with myopathies of unknown etiology.

Authors:  Khadijeh Haji Naghi Tehrani; Elmira Sakhaeyan; Elnaz Sakhaeyan
Journal:  Electron Physician       Date:  2017-07-25

10.  A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromes.

Authors:  Igor Ribeiro Ferreira; Régis Afonso Costa; Leonardo Henrique Ferreira Gomes; Wilton Darleans Dos Santos Cunha; Latife Salomão Tyszler; Silvia Freitas; Juan Clinton Llerena Junior; Zilton Farias Meira de Vasconcelos; Robert D Nicholls; Letícia da Cunha Guida
Journal:  Sci Rep       Date:  2020-08-03       Impact factor: 4.379

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