Literature DB >> 29880332

Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease.

Marco Savarese1, Annalaura Torella2, Olimpia Musumeci3, Corrado Angelini4, Guja Astrea5, Luca Bello6, Claudio Bruno7, Giacomo Pietro Comi8, Giuseppina Di Fruscio9, Giulio Piluso9, Giuseppe Di Iorio10, Manuela Ergoli11, Gaia Esposito9, Marina Fanin6, Olimpia Farina10, Chiara Fiorillo7, Arcomaria Garofalo9, Teresa Giugliano9, Francesca Magri8, Carlo Minetti7, Maurizio Moggio12, Luigia Passamano11, Elena Pegoraro6, Ester Picillo11, Simone Sampaolo10, Filippo Maria Santorelli5, Claudio Semplicini6, Bjarne Udd13, Antonio Toscano3, Luisa Politano14, Vincenzo Nigro2.   

Abstract

Mutations in the GAA gene may cause a late onset Pompe disease presenting with proximal weakness without the characteristic muscle pathology, and therefore a test for GAA activity is the first tier analysis in all undiagnosed patients with hyperCKemia and/or limb-girdle muscular weakness. By using MotorPlex, a targeted gene panel for next generation sequencing, we analyzed GAA and other muscle disease-genes in a large cohort of undiagnosed patients with suspected inherited skeletal muscle disorders (n = 504). In this cohort, 275 patients presented with limb-girdle phenotype and/or an isolated hyperCKemia. Mutational analysis identified GAA mutations in ten patients. Further seven affected relatives were identified by segregation studies. All the patients carried the common GAA mutation c.-32-13T >G and a second, previously reported mutation. In the subcohort of 275 patients with proximal muscle weakness and/or hyperCKemia, we identified late-onset Pompe disease in 10 patients. The clinical overlap between Pompe disease and LGMDs or other skeletal muscle disorders suggests that GAA and the genes causing a metabolic myopathy should be analyzed in all the gene panels used for testing neuromuscular patients. However, enzymatic tests are essential for the interpretation and validation of genetic results.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  GAA; Gene panels; HyperCKemia; LGMD; Late onset Pompe disease (LOPD); Metabolic myopathies

Mesh:

Substances:

Year:  2018        PMID: 29880332     DOI: 10.1016/j.nmd.2018.03.011

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  5 in total

Review 1.  Diagnostic tools in late onset Pompe disease (LOPD).

Authors:  Olimpia Musumeci; Antonio Toscano
Journal:  Ann Transl Med       Date:  2019-07

2.  Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.

Authors:  Babi Ramesh Reddy Nallamilli; Samya Chakravorty; Akanchha Kesari; Alice Tanner; Arunkanth Ankala; Thomas Schneider; Cristina da Silva; Randall Beadling; John J Alexander; Syed Hussain Askree; Zachary Whitt; Lora Bean; Christin Collins; Satish Khadilkar; Pradnya Gaitonde; Rashna Dastur; Matthew Wicklund; Tahseen Mozaffar; Matthew Harms; Laura Rufibach; Plavi Mittal; Madhuri Hegde
Journal:  Ann Clin Transl Neurol       Date:  2018-12-01       Impact factor: 4.511

3.  The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease.

Authors:  Jorge A Bevilacqua; Maria Del Rosario Guecaimburu Ehuletche; Abayuba Perna; Alberto Dubrovsky; Marcondes C Franca; Steven Vargas; Madhuri Hegde; Kristl G Claeys; Volker Straub; Nadia Daba; Roberta Faria; Magali Periquet; Susan Sparks; Nathan Thibault; Roberto Araujo
Journal:  Orphanet J Rare Dis       Date:  2020-01-13       Impact factor: 4.123

Review 4.  The rapidly evolving view of lysosomal storage diseases.

Authors:  Giancarlo Parenti; Diego L Medina; Andrea Ballabio
Journal:  EMBO Mol Med       Date:  2021-01-18       Impact factor: 12.137

5.  Late-onset myopathies: clinical features and diagnosis.

Authors:  Marianne de Visser
Journal:  Acta Myol       Date:  2020-12-01
  5 in total

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