Literature DB >> 16817011

Improvement in serial cardiopulmonary exercise testing following enzyme replacement therapy in Fabry disease.

Gregory Bierer1, David Balfe, William R Wilcox, Zab Mosenifar.   

Abstract

BACKGROUND: Fabry disease is an X-linked genetic disorder resulting in the accumulation of glycosphingolipids in various organs, leading to exercise intolerance and early mortality. Enzyme replacement therapy (ERT) has recently been approved for use in Fabry patients. GOALS OF STUDY: To assess baseline cardiopulmonary exercise characteristics in both invasive and noninvasive tests and to study the impact of ERT on exercise.
METHODS: A total of 15 patients with Fabry disease underwent baseline cardiopulmonary exercise tests. Six patients were randomized 2:1 to receive either ERT or placebo. We performed serial cardiopulmonary exercise tests at baseline and every 3 months over a period of at least 18 months. The baseline test was compared to the last two exercise tests for each patient.
RESULTS: Mean age was 32 years. Mean VO2max was 1.680 +/- 0.67 L/min and increased by 0.459 +/- 0.64 L/min in the patients receiving ERT. Mean VO2max was 1.462 +/- 0.25 L/min and decreased by 0.116 +/- 0.44 L/min in patients on placebo. Mean oxygen pulse (VO2/HR) increased by 1.71 with enzyme, but increased only 0.025 in patients taking placebo. Estimated stroke volume (SV) increased by 10 ml in patients on ERT.
CONCLUSIONS: In this small cohort, exercise tolerance increased in patients receiving enzyme replacement therapy. Cardiopulmonary exercise testing is a useful test in measuring the response to therapy in Fabry disease patients.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16817011     DOI: 10.1007/s10545-006-0361-5

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


  19 in total

1.  Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Authors:  C M Eng; N Guffon; W R Wilcox; D P Germain; P Lee; S Waldek; L Caplan; G E Linthorst; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

2.  Lung function testing: selection of reference values and interpretative strategies. American Thoracic Society.

Authors: 
Journal:  Am Rev Respir Dis       Date:  1991-11

3.  Chronic airflow obstruction in Fabry's disease.

Authors:  D M Rosenberg; V J Ferrans; J D Fulmer; B R Line; J A Barranger; R O Brady; R G Crystal
Journal:  Am J Med       Date:  1980-06       Impact factor: 4.965

4.  The 1995 update of recommendations for a standard technique for measuring the single-breath carbon monoxide diffusing capacity (transfer factor)

Authors:  E Rosenberg
Journal:  Am J Respir Crit Care Med       Date:  1996-09       Impact factor: 21.405

5.  Cardiac output estimated noninvasively from oxygen uptake during exercise.

Authors:  W W Stringer; J E Hansen; K Wasserman
Journal:  J Appl Physiol (1985)       Date:  1997-03

Review 6.  Pulmonary involvement in Fabry's disease: a reappraisal follow-up of a San Diego kindred and review of literature.

Authors:  E E Bartimmo; M Guisan; K M Moser
Journal:  Am J Med       Date:  1972-12       Impact factor: 4.965

7.  Early detection of Fabry cardiomyopathy by tissue Doppler imaging.

Authors:  Maurizio Pieroni; Cristina Chimenti; Roberta Ricci; Patrizio Sale; Matteo Antonio Russo; Andrea Frustaci
Journal:  Circulation       Date:  2003-03-31       Impact factor: 29.690

8.  Fabry disease: overall effects of agalsidase alfa treatment.

Authors:  M Beck; R Ricci; U Widmer; F Dehout; A García de Lorenzo; C Kampmann; A Linhart; G Sunder-Plassmann; G Houge; U Ramaswami; A Gal; A Mehta
Journal:  Eur J Clin Invest       Date:  2004-12       Impact factor: 4.686

9.  Pulmonary involvement in Fabry disease.

Authors:  L K Brown; A Miller; A Bhuptani; M F Sloane; M I Zimmerman; G Schilero; C M Eng; R J Desnick
Journal:  Am J Respir Crit Care Med       Date:  1997-03       Impact factor: 21.405

Review 10.  Tissue Doppler imaging in Fabry disease.

Authors:  Maurizio Pieroni; Cristina Chimenti; Andrea Russo; Matteo Antonio Russo; Attilio Maseri; Andrea Frustaci
Journal:  Curr Opin Cardiol       Date:  2004-09       Impact factor: 2.161

View more
  14 in total

Review 1.  Natural course of Fabry disease and the effectiveness of enzyme replacement therapy: a systematic review and meta-analysis: effectiveness of ERT in different disease stages.

Authors:  Saskia M Rombach; Bouwien E Smid; Gabor E Linthorst; Marcel G W Dijkgraaf; Carla E M Hollak
Journal:  J Inherit Metab Dis       Date:  2014-02-04       Impact factor: 4.982

Review 2.  Enzyme replacement therapy for Anderson-Fabry disease.

Authors:  Regina El Dib; Huda Gomaa; Raíssa Pierri Carvalho; Samira E Camargo; Rodrigo Bazan; Pasqual Barretti; Fellype C Barreto
Journal:  Cochrane Database Syst Rev       Date:  2016-07-25

Review 3.  Enzyme replacement therapy for Fabry disease: a systematic review of available evidence.

Authors:  Roland M Schaefer; Anna Tylki-Szymańska; Max J Hilz
Journal:  Drugs       Date:  2009-11-12       Impact factor: 9.546

4.  Enzyme replacement therapy stabilizes obstructive pulmonary Fabry disease associated with respiratory globotriaosylceramide storage.

Authors:  R Y Wang; J T Abe; A H Cohen; W R Wilcox
Journal:  J Inherit Metab Dis       Date:  2008-10-21       Impact factor: 4.982

5.  Enzyme replacement therapy for Fabry disease: A systematic review and meta-analysis.

Authors:  Taciane Alegra; Filippo Vairo; Monica V de Souza; Bárbara C Krug; Ida V D Schwartz
Journal:  Genet Mol Biol       Date:  2012-12-18       Impact factor: 1.771

6.  Enzyme replacement therapy for Fabry disease: some answers but more questions.

Authors:  Majid Alfadhel; Sandra Sirrs
Journal:  Ther Clin Risk Manag       Date:  2011-02-25       Impact factor: 2.423

7.  Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document.

Authors:  Marieke Biegstraaten; Reynir Arngrímsson; Frederic Barbey; Lut Boks; Franco Cecchi; Patrick B Deegan; Ulla Feldt-Rasmussen; Tarekegn Geberhiwot; Dominique P Germain; Chris Hendriksz; Derralynn A Hughes; Ilkka Kantola; Nesrin Karabul; Christine Lavery; Gabor E Linthorst; Atul Mehta; Erica van de Mheen; João P Oliveira; Rossella Parini; Uma Ramaswami; Michael Rudnicki; Andreas Serra; Claudia Sommer; Gere Sunder-Plassmann; Einar Svarstad; Annelies Sweeb; Wim Terryn; Anna Tylki-Szymanska; Camilla Tøndel; Bojan Vujkovac; Frank Weidemann; Frits A Wijburg; Peter Woolfson; Carla E M Hollak
Journal:  Orphanet J Rare Dis       Date:  2015-03-27       Impact factor: 4.123

8.  A single lung transplant in a patient with fabry disease: causality or far-fetched? A case report.

Authors:  Martina Gaggl; Renate Kain; Peter Jaksch; Dominik Haider; Gerald Mundigler; Till Voigtländer; Raute Sunder-Plassmann; Paulus Rommer; Walter Klepetko; Gere Sunder-Plassmann
Journal:  Case Rep Transplant       Date:  2013-04-07

9.  Twenty-four-month alpha-galactosidase A replacement therapy in Fabry disease has only minimal effects on symptoms and cardiovascular parameters.

Authors:  J W Koskenvuo; J J Hartiala; P Nuutila; R Kalliokoski; J S Viikari; E Engblom; M Penttinen; J Knuuti; I Mononen; I M Kantola
Journal:  J Inherit Metab Dis       Date:  2008-05-23       Impact factor: 4.750

Review 10.  Fabry disease, respiratory symptoms, and airway limitation - a systematic review.

Authors:  Camilla Kara Svensson; Ulla Feldt-Rasmussen; Vibeke Backer
Journal:  Eur Clin Respir J       Date:  2015-06-26
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.