Literature DB >> 22926198

Effect of rapid cessation of enzyme replacement therapy: a report of 5 cases and a review of the literature.

Agnieszka Jurecka1, Zbigniew Żuberuber, Violetta Opoka-Winiarska, Grzegorz Węgrzyn, Anna Tylki-Szymańska.   

Abstract

UNLABELLED: Enzyme replacement therapy (ERT) is a treatment modality available for several of the lysosomal storage diseases including mucopolysaccharidosis type II (MPS II). We report a series of patients with MPS II (n = 5, age range at the start of ERT 11-21 years, median 15 years) and the effects of ERT cessation (range 2-8 months, median 3 months) on their clinical status. Additionally, we review previously published cases. In our series, a worsening of the patients' clinical status was observed. Symptoms after ERT discontinuation included recurrent respiratory infections (severe pneumonia) with respiratory insufficiency (80%), difficulty with walking/standing (60%), increased joint stiffness (40%), but also decreased hematological parameters (40%), renal insufficiency (40%) and death (20%). The literature review confirms that the beneficial clinical effects of ERT are soon lost if treatment is discontinued in MPS I and Pompe patients.
CONCLUSIONS: 1. Rapid cessation of ERT results not only in the loss of the beneficial effects, but in a significant worsening of the patient's clinical status. 2. Decisions about the introduction of ERT, especially in patients severely affected, should be made carefully. 3. Once started, it is essential to keep an adequate administration schedule of ERT to maintain the clinical benefits of enzyme therapy.
Copyright © 2012 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22926198     DOI: 10.1016/j.ymgme.2012.08.013

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  10 in total

1.  Enzyme replacement in neuronal storage disorders in the pediatric population.

Authors:  Erika F Augustine; Jonathan W Mink
Journal:  Curr Treat Options Neurol       Date:  2013-10       Impact factor: 3.598

2.  Cessation and resuming of alglucosidase alfa in Pompe disease: a retrospective analysis.

Authors:  Thomas Hundsberger; Kai M Rösler; Oliver Findling
Journal:  J Neurol       Date:  2014-06-13       Impact factor: 4.849

3.  Safety of Intradiaphragmatic Delivery of Adeno-Associated Virus-Mediated Alpha-Glucosidase (rAAV1-CMV-hGAA) Gene Therapy in Children Affected by Pompe Disease.

Authors:  Manuela Corti; Cristina Liberati; Barbara K Smith; Lee Ann Lawson; Ibrahim S Tuna; Thomas J Conlon; Kirsten E Coleman; Saleem Islam; Roland W Herzog; David D Fuller; Shelley W Collins; Barry J Byrne
Journal:  Hum Gene Ther Clin Dev       Date:  2017-12       Impact factor: 5.032

Review 4.  Treatment of mucopolysaccharidosis type II (Hunter syndrome): results from a systematic evidence review.

Authors:  Linda A Bradley; Hamish R M Haddow; Glenn E Palomaki
Journal:  Genet Med       Date:  2017-05-18       Impact factor: 8.822

Review 5.  Intravenous Enzyme Replacement Therapy in Mucopolysaccharidoses: Clinical Effectiveness and Limitations.

Authors:  Rossella Parini; Federica Deodato
Journal:  Int J Mol Sci       Date:  2020-04-23       Impact factor: 5.923

6.  Enzyme replacement therapy interruption in mucopolysaccharidosis type IVA patients and its impact in different clinical outcomes.

Authors:  Juan Politei; Gloria Liliana Porras-Hurtado; Norberto Guelbert; Alejandro Fainboim; Dafne Dain Gandelman Horovitz; José María Satizábal
Journal:  JIMD Rep       Date:  2021-01-12

Review 7.  Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future.

Authors:  David Ah Whiteman; Alan Kimura
Journal:  Drug Des Devel Ther       Date:  2017-08-23       Impact factor: 4.162

8.  Advancements in AAV-mediated Gene Therapy for Pompe Disease.

Authors:  S M Salabarria; J Nair; N Clement; B K Smith; N Raben; D D Fuller; B J Byrne; M Corti
Journal:  J Neuromuscul Dis       Date:  2020

9.  Enzyme replacement therapy interruption in patients with Mucopolysaccharidoses: Recommendations for distinct scenarios in Latin America.

Authors:  MarthaL Solano; Alejandro Fainboim; Juan Politei; Gloria L Porras-Hurtado; Ana Maria Martins; Carolina F Moura Souza; Felipe Mendez Koch; Hernan Amartino; Jose Maria Satizábal; Dafne D G Horovitz; Paula F V Medeiros; Rachel S Honjo; Charles M Lourenço
Journal:  Mol Genet Metab Rep       Date:  2020-02-27

10.  Transcriptomic analyses suggest that mucopolysaccharidosis patients may be less susceptible to COVID-19.

Authors:  Karolina Pierzynowska; Lidia Gaffke; Grzegorz Węgrzyn
Journal:  FEBS Lett       Date:  2020-09-06       Impact factor: 3.864

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.