Literature DB >> 31899940

Pulmonary outcome measures in long-term survivors of infantile Pompe disease on enzyme replacement therapy: A case series.

Mai K ElMallah1, Ankit K Desai2, Erica B Nading2, Stephanie DeArmey2, Richard M Kravitz1, Priya S Kishnani2.   

Abstract

OBJECTIVES: To report the respiratory function of school-aged children with infantile Pompe disease (IPD) who started enzyme replacement therapy (ERT) in infancy and early childhood. STUDY
DESIGN: This is a retrospective chart review of pulmonary function tests of: (a) patients with IPD 5 to 18 years of age, (b) who were not ventilator dependent, and (c) were able to perform upright and supine spirometry. Subjects were divided into a younger (5-9 years) and older cohort (10-18 years) for the analysis. Upright and supine forced vital capacity (FVC), maximal inspiratory pressure (MIP), and maximal expiratory pressure (MEP) were analyzed.
RESULTS: Fourteen patients, all cross-reactive immunologic material (CRIM)-positive, met the inclusion criteria and were included in this study. Mean upright and supine FVC were 70.3% and 64.9% predicted, respectively, in the 5- to 9-year-old cohort; and 61.5% and 52.5% predicted, respectively, in the 10- to 18-year-old group. Individual patient trends showed stability in FVC overtime in six of the 14 patients. MIPs and MEPs were consistent with inspiratory and expiratory muscle weakness in the younger and older age group but did not decline with age.
CONCLUSION: Data from this cohort of CRIM-positive patients with IPD showed that ERT is able to maintain respiratory function in a subgroup of patients whereas others had a steady decline. There was a statistically significant decline in FVC from the upright to a supine position in both the younger and older age groups of CRIM-positive ERT-treated patients. Before ERT, patients with IPD were unable to maintain independent ventilation beyond the first few years of life.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  enzyme replacement therapy; infantile Pompe disease; pulmonary function testing

Mesh:

Year:  2020        PMID: 31899940      PMCID: PMC7053514          DOI: 10.1002/ppul.24621

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  52 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
Journal:  J Pediatr       Date:  2000-08       Impact factor: 4.406

2.  Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation.

Authors:  Alberto Dubrovsky; Jose Corderi; Min Lin; Priya S Kishnani; Harrison N Jones
Journal:  Muscle Nerve       Date:  2011-09-26       Impact factor: 3.217

3.  The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease.

Authors:  P Laforêt; K Laloui; B Granger; D Hamroun; N Taouagh; J-Y Hogrel; D Orlikowski; F Bouhour; A Lacour; E Salort-Campana; I Penisson-Besnier; S Sacconi; F Zagnoli; F Chapon; B Eymard; C Desnuelle; J Pouget
Journal:  Rev Neurol (Paris)       Date:  2013-09-03       Impact factor: 2.607

4.  Spanish Pompe registry: Baseline characteristics of first 49 patients with adult onset of Pompe disease.

Authors:  Jorge Alonso-Pérez; Sonia Segovia; Cristina Domínguez-González; Montse Olivé; María Dolores Mendoza Grimón; Roberto Fernández-Torrón; Adolfo López de Munain; José Luis Muñoz-Blanco; Alba Ramos-Fransi; Miriam Almendrote; Isabel Illa; Jordi Díaz-Manera
Journal:  Med Clin (Barc)       Date:  2019-06-26       Impact factor: 1.725

Review 5.  Clinical and histologic ocular findings in pompe disease.

Authors:  Tammy L Yanovitch; Suhrad G Banugaria; Alan D Proia; Priya S Kishnani
Journal:  J Pediatr Ophthalmol Strabismus       Date:  2010-01-21       Impact factor: 1.402

Review 6.  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

7.  Neural deficits contribute to respiratory insufficiency in Pompe disease.

Authors:  Lara R DeRuisseau; David D Fuller; Kai Qiu; Keith C DeRuisseau; William H Donnelly; Cathryn Mah; Paul J Reier; Barry J Byrne
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

8.  Effect of enzyme therapy and prognostic factors in 69 adults with Pompe disease: an open-label single-center study.

Authors:  Juna M de Vries; Nadine A M E van der Beek; Wim C J Hop; Francois P J Karstens; John H Wokke; Marianne de Visser; Baziel G M van Engelen; Jan B M Kuks; Anneke J van der Kooi; Nicolette C Notermans; Catharina G Faber; Jan J G M Verschuuren; Michelle E Kruijshaar; Arnold J J Reuser; Pieter A van Doorn; Ans T van der Ploeg
Journal:  Orphanet J Rare Dis       Date:  2012-09-26       Impact factor: 4.123

9.  Pompe disease diagnosis and management guideline.

Authors:  Priya S Kishnani; Robert D Steiner; Deeksha Bali; Kenneth Berger; Barry J Byrne; Laura E Case; Laura Case; John F Crowley; Steven Downs; R Rodney Howell; Richard M Kravitz; Joanne Mackey; Deborah Marsden; Anna Maria Martins; David S Millington; Marc Nicolino; Gwen O'Grady; Marc C Patterson; David M Rapoport; Alfred Slonim; Carolyn T Spencer; Cynthia J Tifft; Michael S Watson
Journal:  Genet Med       Date:  2006-05       Impact factor: 8.822

10.  Effects of a higher dose of alglucosidase alfa on ventilator-free survival and motor outcome in classic infantile Pompe disease: an open-label single-center study.

Authors:  C M van Gelder; E Poelman; I Plug; M Hoogeveen-Westerveld; N A M E van der Beek; A J J Reuser; A T van der Ploeg
Journal:  J Inherit Metab Dis       Date:  2016-01-14       Impact factor: 4.982

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  2 in total

1.  Lentiviral Hematopoietic Stem Cell Gene Therapy Rescues Clinical Phenotypes in a Murine Model of Pompe Disease.

Authors:  Giuseppa Piras; Claudia Montiel-Equihua; Yee-Ka Agnes Chan; Slawomir Wantuch; Daniel Stuckey; Derek Burke; Helen Prunty; Rahul Phadke; Darren Chambers; Armando Partida-Gaytan; Diego Leon-Rico; Neelam Panchal; Kathryn Whitmore; Miguel Calero; Sara Benedetti; Giorgia Santilli; Adrian J Thrasher; H Bobby Gaspar
Journal:  Mol Ther Methods Clin Dev       Date:  2020-07-06       Impact factor: 6.698

Review 2.  The Respiratory Phenotype of Pompe Disease Mouse Models.

Authors:  Anna F Fusco; Angela L McCall; Justin S Dhindsa; Lucy Zheng; Aidan Bailey; Amanda F Kahn; Mai K ElMallah
Journal:  Int J Mol Sci       Date:  2020-03-24       Impact factor: 5.923

  2 in total

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