Literature DB >> 24906254

Effectiveness of enzyme replacement therapy in adults with late-onset Pompe disease: results from the NCS-LSD cohort study.

L J Anderson1, W Henley, K M Wyatt, V Nikolaou, S Waldek, D A Hughes, R H Lachmann, S Logan.   

Abstract

OBJECTIVES: To determine the effectiveness of enzyme replacement therapy (ERT) for adults with late-onset Pompe disease.
DESIGN: A longitudinal cohort study including prospective and retrospective clinical outcome data. Age- and gender-adjusted treatment effects were estimated using generalised linear mixed models. Treated patients contributed data before and during treatment. Untreated patients contributed natural history data. PARTICIPANTS: Consenting adults (N = 62) with a diagnosis of late-onset Pompe disease who attended a specialist treatment centre in England. This cohort represented 83 % of all patients in the UK with a confirmed diagnosis of this rare condition. At study entry, all but three patients were receiving ERT (range of treatment duration, 0 to 3.1 years). OUTCOME MEASURES: Percent predicted forced vital capacity (%FVC); ventilation dependency; mobility; 6 min walk test (6MWT); muscle strength and body mass index (BMI).
RESULTS: An association was found between time on ERT and significant increases in the distance walked in the 6MWT (p < 0.001) and muscle strength scores (p < 0.001). Improvements in both these measures were seen over the first 2 years of treatment with ERT. No statistically significant relationship was found between time on ERT and respiratory function or in BMI.
CONCLUSIONS: These data provide some further evidence of the effectiveness of ERT in adults with late-onset Pompe disease. SYNOPSIS: The results of this longitudinal cohort study of 62 adults with late-onset Pompe disease, provide further evidence on the effectiveness of ERT in this rare condition.

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Year:  2014        PMID: 24906254     DOI: 10.1007/s10545-014-9728-1

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  29 in total

1.  Identification of two subtypes of infantile acid maltase deficiency.

Authors:  A E Slonim; L Bulone; S Ritz; T Goldberg; A Chen; F Martiniuk
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2.  A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease.

Authors:  Priya S Kishnani; Wuh-Liang Hwu; Hanna Mandel; Marc Nicolino; Florence Yong; Deyanira Corzo
Journal:  J Pediatr       Date:  2006-05       Impact factor: 4.406

3.  Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease.

Authors:  N A M E Van der Beek; M L C Hagemans; A J J Reuser; W C J Hop; A T Van der Ploeg; P A Van Doorn; J H J Wokke
Journal:  Neuromuscul Disord       Date:  2008-12-11       Impact factor: 4.296

4.  Recombinant human alpha-glucosidase from rabbit milk in Pompe patients.

Authors:  H Van den Hout; A J Reuser; A G Vulto; M C Loonen; A Cromme-Dijkhuis; A T Van der Ploeg
Journal:  Lancet       Date:  2000-07-29       Impact factor: 79.321

5.  Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years.

Authors:  C Angelini; C Semplicini; S Ravaglia; B Bembi; S Servidei; E Pegoraro; M Moggio; M Filosto; E Sette; G Crescimanno; P Tonin; R Parini; L Morandi; G Marrosu; G Greco; O Musumeci; G Di Iorio; G Siciliano; M A Donati; F Carubbi; M Ermani; T Mongini; A Toscano
Journal:  J Neurol       Date:  2011-11-12       Impact factor: 4.849

6.  Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease.

Authors:  P S Kishnani; D Corzo; M Nicolino; B Byrne; H Mandel; W L Hwu; N Leslie; J Levine; C Spencer; M McDonald; J Li; J Dumontier; M Halberthal; Y H Chien; R Hopkin; S Vijayaraghavan; D Gruskin; D Bartholomew; A van der Ploeg; J P Clancy; R Parini; G Morin; M Beck; G S De la Gastine; M Jokic; B Thurberg; S Richards; D Bali; M Davison; M A Worden; Y T Chen; J E Wraith
Journal:  Neurology       Date:  2006-12-06       Impact factor: 9.910

7.  Pompe disease: dramatic improvement in gastrointestinal function following enzyme replacement therapy. A report of three later-onset patients.

Authors:  Donna L Bernstein; Martin G Bialer; Lakshmi Mehta; Robert J Desnick
Journal:  Mol Genet Metab       Date:  2010-06-22       Impact factor: 4.797

Review 8.  The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature.

Authors:  Hannerieke M P van den Hout; Wim Hop; Otto P van Diggelen; Jan A M Smeitink; G Peter A Smit; Bwee-Tien T Poll-The; Henk D Bakker; M Christa B Loonen; Johannis B C de Klerk; Arnold J J Reuser; Ans T van der Ploeg
Journal:  Pediatrics       Date:  2003-08       Impact factor: 7.124

Review 9.  Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review.

Authors:  Antonio Toscano; Benedikt Schoser
Journal:  J Neurol       Date:  2012-08-28       Impact factor: 4.849

10.  The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disorders.

Authors:  K Wyatt; W Henley; L Anderson; R Anderson; V Nikolaou; K Stein; L Klinger; D Hughes; S Waldek; R Lachmann; A Mehta; A Vellodi; S Logan
Journal:  Health Technol Assess       Date:  2012       Impact factor: 4.014

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  17 in total

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2.  Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatment.

Authors:  Federica Montagnese; E Barca; O Musumeci; S Mondello; A Migliorato; A Ciranni; C Rodolico; P De Filippi; C Danesino; A Toscano
Journal:  J Neurol       Date:  2015-02-12       Impact factor: 4.849

Review 3.  Disease models for the development of therapies for lysosomal storage diseases.

Authors:  Miao Xu; Omid Motabar; Marc Ferrer; Juan J Marugan; Wei Zheng; Elizabeth A Ottinger
Journal:  Ann N Y Acad Sci       Date:  2016-05-04       Impact factor: 5.691

Review 4.  Survival and long-term outcomes in late-onset Pompe disease following alglucosidase alfa treatment: a systematic review and meta-analysis.

Authors:  Benedikt Schoser; Andrew Stewart; Steve Kanters; Alaa Hamed; Jeroen Jansen; Keith Chan; Mohammad Karamouzian; Antonio Toscano
Journal:  J Neurol       Date:  2016-07-02       Impact factor: 4.849

5.  Quantification of intramuscular fat in patients with late-onset Pompe disease by conventional magnetic resonance imaging for the long-term follow-up of enzyme replacement therapy.

Authors:  André Lollert; Clemens Stihl; Andreas M Hötker; Eugen Mengel; Jochem König; Katharina Laudemann; Seyfullah Gökce; Christoph Düber; Gundula Staatz
Journal:  PLoS One       Date:  2018-01-09       Impact factor: 3.240

6.  GAA Deficiency in Pompe Disease Is Alleviated by Exon Inclusion in iPSC-Derived Skeletal Muscle Cells.

Authors:  Erik van der Wal; Atze J Bergsma; Tom J M van Gestel; Stijn L M In 't Groen; Holm Zaehres; Marcos J Araúzo-Bravo; Hans R Schöler; Ans T van der Ploeg; W W M Pim Pijnappel
Journal:  Mol Ther Nucleic Acids       Date:  2017-03-14

7.  Enzyme replacement therapy reduces the risk for wheelchair dependency in adult Pompe patients.

Authors:  Jan C van der Meijden; Michelle E Kruijshaar; Dimitris Rizopoulos; Pieter A van Doorn; Nadine A M E van der Beek; Ans T van der Ploeg
Journal:  Orphanet J Rare Dis       Date:  2018-05-22       Impact factor: 4.123

8.  Positive association between physical outcomes and patient-reported outcomes in late-onset Pompe disease: a cross sectional study.

Authors:  Meng Yuan; Eleni-Rosalina Andrinopoulou; Michelle E Kruijshaar; Aglina Lika; Laurike Harlaar; Ans T van der Ploeg; Dimitris Rizopoulos; Nadine A M E van der Beek
Journal:  Orphanet J Rare Dis       Date:  2020-09-03       Impact factor: 4.123

9.  Effect of enzyme replacement therapy (ERT) added to Home Mechanical Ventilation (HMV) in Adult Pompe disease.

Authors:  Nadia Sayeed; Pooja Sharma; Manahil Abdelhalim; Rahul Mukherjee
Journal:  Respirol Case Rep       Date:  2015-11-19

10.  Satellite cells fail to contribute to muscle repair but are functional in Pompe disease (glycogenosis type II).

Authors:  Lydie Lagalice; Julien Pichon; Eliot Gougeon; Salwa Soussi; Johan Deniaud; Mireille Ledevin; Virginie Maurier; Isabelle Leroux; Sylvie Durand; Carine Ciron; Francesca Franzoso; Laurence Dubreil; Thibaut Larcher; Karl Rouger; Marie-Anne Colle
Journal:  Acta Neuropathol Commun       Date:  2018-10-31       Impact factor: 7.801

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