Literature DB >> 28625968

Long-Term Dose-Dependent Agalsidase Effects on Kidney Histology in Fabry Disease.

Rannveig Skrunes1,2, Camilla Tøndel2,3, Sabine Leh2,4, Kristin Kampevold Larsen4, Gunnar Houge5, Einar Skulstad Davidsen6, Carla Hollak7,8, André B P van Kuilenburg9, Frédéric M Vaz9, Einar Svarstad10,2.   

Abstract

BACKGROUND AND OBJECTIVES: Dose-dependent clearing of podocyte globotriaosylceramide has previously been shown in patients with classic Fabry disease treated with enzyme replacement. Our study evaluates the dose-dependent effects of agalsidase therapy in serial kidney biopsies of patients treated for up to 14 years. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Twenty patients with classic Fabry disease (12 men) started enzyme replacement therapy at a median age of 21 (range =7-62) years old. Agalsidase-α or -β was prescribed for a median of 9.4 (range =5-14) years. The lower fixed dose group received agalsidase 0.2 mg/kg every other week throughout the follow-up period. The higher dose group received a range of agalsidase doses (0.2-1.0 mg/kg every other week). Dose changes were made due to disease progression, suboptimal effect, or agalsidase-β shortage. Serial kidney biopsies were performed along with clinical assessment and biomarkers and scored according to recommendations from the International Study Group of Fabry Nephropathy.
RESULTS: No statistical differences were found in baseline or final GFR or albuminuria. Kidney biopsies showed significant reduction of podocyte globotriaosylceramide in both the lower fixed dose group (-1.39 [SD=1.04]; P=0.004) and the higher dose group (-3.16 [SD=2.39]; P=0.002). Podocyte globotriaosylceramide (Gb3) reduction correlated with cumulative agalsidase dose (r=0.69; P=0.001). Arterial/arteriolar intima Gb3 cleared significantly in the higher dose group, all seven patients with baseline intimal Gb3 cleared the intima, one patient gained intimal Gb3 inclusions (P=0.03), and medial Gb3 did not change statistically in either group. Residual plasma globotriaosylsphingosine levels remained higher in the lower fixed dose group (20.1 nmol/L [SD=11.9]) compared with the higher dose group (10.4 nmol/L [SD=8.4]) and correlated with cumulative agalsidase dose in men (r=0.71; P=0.01).
CONCLUSIONS: Reduction of podocyte globotriaosylceramide was found in patients with classic Fabry disease treated with long-term agalsidase on different dosing regimens, correlating with cumulative dose. Limited clearing of arterial/arteriolar globotriaosylceramide raises concerns regarding long-term vascular effects of current therapy. Residual plasma globotriaosylsphingosine correlated with cumulative dose in men.
Copyright © 2017 by the American Society of Nephrology.

Entities:  

Keywords:  Adolescent; Adult; Biomarkers; Biopsy; Child; Disease Progression; Enzyme Replacement Therapy; Fabry Disease; Follow-Up Studies; Humans; Isoenzymes; Male; Middle Aged; Podocytes; Trihexosylceramides; Young Adult; albuminuria; alpha-Galactosidas; chronic kidney disease; genetic renal disease; glomerular filtration rate; podocyte

Mesh:

Substances:

Year:  2017        PMID: 28625968      PMCID: PMC5586567          DOI: 10.2215/CJN.01820217

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  43 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.  Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortage.

Authors:  Gabor E Linthorst; Alessandro P Burlina; Franco Cecchi; Timothy M Cox; Janice M Fletcher; Ulla Feldt-Rasmussen; Roberto Giugliani; Carla E M Hollak; Gunnar Houge; Derralynn Hughes; Iikka Kantola; Robin Lachmann; Monica Lopez; Alberto Ortiz; Rossella Parini; Alberto Rivera; Arndt Rolfs; Uma Ramaswami; Einar Svarstad; Camilla Tondel; Anna Tylki-Szymanska; Bojan Vujkovac; Steven Waldek; Michael West; F Weidemann; Atul Mehta
Journal:  JIMD Rep       Date:  2012-07-14

Review 3.  Fabry disease (alpha-galactosidase A deficiency): renal involvement and enzyme replacement therapy.

Authors:  R J Desnick; M P Wasserstein; M Banikazemi
Journal:  Contrib Nephrol       Date:  2001       Impact factor: 1.580

4.  Reduction of elevated plasma globotriaosylsphingosine in patients with classic Fabry disease following enzyme replacement therapy.

Authors:  Mariëlle J van Breemen; Saskia M Rombach; Nick Dekker; Ben J Poorthuis; Gabor E Linthorst; Aeilko H Zwinderman; Frank Breunig; Christoph Wanner; Johannes M Aerts; Carla E Hollak
Journal:  Biochim Biophys Acta       Date:  2010-09-17

5.  Screening, diagnosis, and management of patients with Fabry disease: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference.

Authors:  Raphael Schiffmann; Derralynn A Hughes; Gabor E Linthorst; Alberto Ortiz; Einar Svarstad; David G Warnock; Michael L West; Christoph Wanner
Journal:  Kidney Int       Date:  2016-12-18       Impact factor: 10.612

6.  Enzyme replacement therapy in Fabry disease: a randomized controlled trial.

Authors:  R Schiffmann; J B Kopp; H A Austin; S Sabnis; D F Moore; T Weibel; J E Balow; R O Brady
Journal:  JAMA       Date:  2001-06-06       Impact factor: 56.272

7.  Geometric method for measuring body surface area: a height-weight formula validated in infants, children, and adults.

Authors:  G B Haycock; G J Schwartz; D H Wisotsky
Journal:  J Pediatr       Date:  1978-07       Impact factor: 4.406

8.  Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease.

Authors:  Dominique P Germain; Joel Charrow; Robert J Desnick; Nathalie Guffon; Judy Kempf; Robin H Lachmann; Roberta Lemay; Gabor E Linthorst; Seymour Packman; C Ronald Scott; Stephen Waldek; David G Warnock; Neal J Weinreb; William R Wilcox
Journal:  J Med Genet       Date:  2015-03-20       Impact factor: 6.318

9.  Urinary Podocyte Loss Is Increased in Patients with Fabry Disease and Correlates with Clinical Severity of Fabry Nephropathy.

Authors:  Brent Fall; C Ronald Scott; Michael Mauer; Stuart Shankland; Jeffrey Pippin; Jonathan A Jefferson; Eric Wallace; David Warnock; Behzad Najafian
Journal:  PLoS One       Date:  2016-12-16       Impact factor: 3.240

10.  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

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  20 in total

Review 1.  Effects of Enzyme Replacement Therapy and Antidrug Antibodies in Patients with Fabry Disease.

Authors:  Malte Lenders; Eva Brand
Journal:  J Am Soc Nephrol       Date:  2018-08-09       Impact factor: 10.121

2.  The Changing Landscape of Fabry Disease.

Authors:  Einar Svarstad; Hans Peter Marti
Journal:  Clin J Am Soc Nephrol       Date:  2020-03-04       Impact factor: 8.237

3.  A classic variant of Fabry disease in a family with the M296I late-onset variant.

Authors:  Shuma Hirashio; Reiko Kagawa; Go Tajima; Takao Masaki
Journal:  CEN Case Rep       Date:  2020-09-09

4.  Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?

Authors:  Juan Politei; Valeria Alberton; Oscar Amoreo; Norberto Antongiovanni; Maria Nieves Arán; Marcelo Barán; Gustavo Cabrera; Silvia Di Pietrantonio; Consuelo Durand; Alejandro Fainboim; Joaquin Frabasil; Fernando Gomez Pizarro; Roberto Iotti; Miguel Liern; Fernando Perretta; Diego Ripeau; Fernanda Toniolo; Hernan Trimarchi; Dana Velasques Rivas; Eric Wallace; Andrea Beatriz Schenone
Journal:  Pediatr Nephrol       Date:  2018-07-09       Impact factor: 3.714

5.  Accumulation of Globotriaosylceramide in Podocytes in Fabry Nephropathy Is Associated with Progressive Podocyte Loss.

Authors:  Behzad Najafian; Camilla Tøndel; Einar Svarstad; Marie-Claire Gubler; João-Paulo Oliveira; Michael Mauer
Journal:  J Am Soc Nephrol       Date:  2020-03-03       Impact factor: 10.121

6.  Unexpectedly high renal pathological scores of two female siblings with Fabry disease presenting with urinary mulberry cells without microalbuminuria.

Authors:  Natsuo Yamada; Hirofumi Sakuma; Mitsuru Yanai; Ayana Suzuki; Keisuke Maruyama; Motoki Matsuki; Naoki Nakagawa
Journal:  Mol Genet Metab Rep       Date:  2022-04-22

7.  Clinical course and pathological findings of two late-onset Fabry hemizygous patients including mulberry cell counts after enzyme replacement therapy.

Authors:  Homare Shimohata; Marina Yamashita; Kentaro Ohgi; Hiroshi Maruyama; Mamiko Takayasu; Kouichi Hirayama; Masaki Kobayashi
Journal:  CEN Case Rep       Date:  2020-03-18

8.  Brazilian consensus recommendations for the diagnosis, screening, and treatment of individuals with fabry disease: Committee for Rare Diseases - Brazilian Society of Nephrology/2021.

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

Review 9.  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

10.  Massive accumulation of globotriaosylceramide in various tissues from a Fabry patient with a high antibody titer against alpha-galactosidase A after 6 years of enzyme replacement therapy.

Authors:  Kenichi Hongo; Toru Harada; Eiko Fukuro; Masahisa Kobayashi; Toya Ohashi; Yoshikatsu Eto
Journal:  Mol Genet Metab Rep       Date:  2020-07-16
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