Literature DB >> 24831586

Long-term effectiveness of enzyme replacement therapy in Fabry disease: results from the NCS-LSD cohort study.

L J Anderson1, K M Wyatt, W Henley, V Nikolaou, S Waldek, D A Hughes, G M Pastores, S Logan.   

Abstract

OBJECTIVES: To determine the effectiveness of enzyme replacement therapy (ERT) for adults and children with Fabry disease.
DESIGN: Cohort study including prospective and retrospective clinical data. Age- and gender-adjusted treatment effects were estimated using generalised linear mixed models. Treated patients contributed data before and during treatment and untreated patients contributed natural history data. PARTICIPANTS: Consenting adults (N = 289) and children (N = 22) with a confirmed diagnosis of Fabry disease attending a specialist Lysosomal Storage Disorder treatment centre in England. At recruitment 211 adults and seven children were on ERT (range of treatment duration, 0 to 9.7 and 0 to 4.2 years respectively). OUTCOME MEASURES: Clinical outcomes chosen to reflect disease progression included left ventricular mass index (LVMI); proteinuria; estimated glomerular filtration rate (eGFR); pain; hearing and transient ischaemic attacks (TIA)/stroke.
RESULTS: We found evidence of a statistically significant association between time on ERT and a small linear decrease in LVMI (p = 0.01); a reduction in the risk of proteinuria after adjusting for angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (p < 0.001) and a small increase in eGFR in men and women without pre-treatment proteinuria (p = 0.01 and p < 0.001 respectively). The same analyses in children provided no statistically significant results. No associations between time on ERT and pain, risk of needing a hearing aid, or risk of stroke or TIAs, were found.
CONCLUSIONS: These data provide some further evidence on the long-term effectiveness of ERT in adults with Fabry disease, but evidence of effectiveness could not be demonstrated in children.

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Year:  2014        PMID: 24831586     DOI: 10.1007/s10545-014-9717-4

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


  40 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

2.  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

3.  A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies.

Authors:  C M Eng; M Banikazemi; R E Gordon; M Goldman; R Phelps; L Kim; A Gass; J Winston; S Dikman; J T Fallon; S Brodie; C B Stacy; D Mehta; R Parsons; K Norton; M O'Callaghan; R J Desnick
Journal:  Am J Hum Genet       Date:  2001-02-01       Impact factor: 11.025

4.  Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy.

Authors:  Raphael Schiffmann; David G Warnock; Maryam Banikazemi; Jan Bultas; Gabor E Linthorst; Seymour Packman; Sven Asger Sorensen; William R Wilcox; Robert J Desnick
Journal:  Nephrol Dial Transplant       Date:  2009-02-13       Impact factor: 5.992

5.  Four-year prospective clinical trial of agalsidase alfa in children with Fabry disease.

Authors:  Raphael Schiffmann; Rick A Martin; Tyler Reimschisel; Karen Johnson; Victoria Castaneda; Y Howard Lien; Gregory M Pastores; Christoph Kampmann; Markus Ries; Joe T R Clarke
Journal:  J Pediatr       Date:  2010-01-25       Impact factor: 4.406

6.  New equations to estimate GFR in children with CKD.

Authors:  George J Schwartz; Alvaro Muñoz; Michael F Schneider; Robert H Mak; Frederick Kaskel; Bradley A Warady; Susan L Furth
Journal:  J Am Soc Nephrol       Date:  2009-01-21       Impact factor: 10.121

7.  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

8.  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

9.  Treatment of Fabry disease: outcome of a comparative trial with agalsidase alfa or beta at a dose of 0.2 mg/kg.

Authors:  Anouk C Vedder; Gabor E Linthorst; Gunnar Houge; Johannna E M Groener; Els E Ormel; Berto J Bouma; Johannes M F G Aerts; Asle Hirth; Carla E M Hollak
Journal:  PLoS One       Date:  2007-07-11       Impact factor: 3.240

10.  Enzyme replacement reverses abnormal cerebrovascular responses in Fabry disease.

Authors:  David F Moore; Gheona Altarescu; Peter Herscovitch; Raphael Schiffmann
Journal:  BMC Neurol       Date:  2002-06-18       Impact factor: 2.474

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  13 in total

1.  A prospective 10-year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease.

Authors:  Raphael Schiffmann; Caren Swift; Xuan Wang; Derek Blankenship; Markus Ries
Journal:  J Inherit Metab Dis       Date:  2015-04-22       Impact factor: 4.982

Review 2.  Lysosomal storage disease overview.

Authors:  Angela Sun
Journal:  Ann Transl Med       Date:  2018-12

3.  Effect and Tolerability of Agalsidase Alfa in Patients with Fabry Disease Who Were Treatment Naïve or Formerly Treated with Agalsidase Beta or Agalsidase Alfa.

Authors:  Ozlem Goker-Alpan; Khan Nedd; Suma P Shankar; Yeong-Hau H Lien; Neal Weinreb; Anna Wijatyk; Peter Chang; Rick Martin
Journal:  JIMD Rep       Date:  2015-03-31

4.  Burden associated with Fabry disease and its treatment in 12-15 year olds: results from a European survey.

Authors:  Lisa Bashorum; Gerard McCaughey; Owen Evans; Ashley C Humphries; Richard Perry; Alasdair MacCulloch
Journal:  Orphanet J Rare Dis       Date:  2022-07-15       Impact factor: 4.303

Review 5.  Anderson-Fabry cardiomyopathy: prevalence, pathophysiology, diagnosis and treatment.

Authors:  Brendan N Putko; Kevin Wen; Richard B Thompson; John Mullen; Miriam Shanks; Haran Yogasundaram; Consolato Sergi; Gavin Y Oudit
Journal:  Heart Fail Rev       Date:  2015-03       Impact factor: 4.214

6.  Long-term enzyme replacement therapy for Fabry disease: efficacy and unmet needs in cardiac and renal outcomes.

Authors:  Ja Hye Kim; Beom Hee Lee; Ja Hyang Cho; Eungu Kang; Jin-Ho Choi; Gu-Hwan Kim; Han-Wook Yoo
Journal:  J Hum Genet       Date:  2016-06-23       Impact factor: 3.172

Review 7.  Recommendations for the diagnosis and management of Fabry disease in pediatric patients: a document from the Rare Diseases Committee of the Brazilian Society of Nephrology (Comdora-SBN).

Authors:  Maria Helena Vaisbich; Luís Gustavo Modelli de Andrade; Cassiano Augusto Braga Silva; Fellype de Carvalho Barreto
Journal:  J Bras Nefrol       Date:  2022 Apr-Jun

8.  Screening for Fabry disease in left ventricular hypertrophy: documentation of a novel mutation.

Authors:  Ana Baptista; Pedro Magalhães; Sílvia Leão; Sofia Carvalho; Pedro Mateus; Ilídio Moreira
Journal:  Arq Bras Cardiol       Date:  2015-08-07       Impact factor: 2.000

9.  Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis.

Authors:  Michael Beck; Derralynn Hughes; Christoph Kampmann; Sylvain Larroque; Atul Mehta; Guillem Pintos-Morell; Uma Ramaswami; Michael West; Anna Wijatyk; Roberto Giugliani
Journal:  Mol Genet Metab Rep       Date:  2015-03-05

10.  Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype.

Authors:  Jin-Ho Choi; Beom Hee Lee; Sun Hee Heo; Gu-Hwan Kim; Yoo-Mi Kim; Dae-Seong Kim; Jung Min Ko; Young Bae Sohn; Yong Hee Hong; Dong-Hwan Lee; Hoon Kook; Han Hyuk Lim; Kyung Hee Kim; Woo-Shik Kim; Geu-Ru Hong; Su-Hyun Kim; Sang Hyun Park; Chan-Duck Kim; So Mi Kim; Jeong-Sook Seo; Han-Wook Yoo
Journal:  Medicine (Baltimore)       Date:  2017-07       Impact factor: 1.889

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