Cardiomyopathy and kidney function in agalsidase beta-treated female Fabry patients: a pre-treatment vs. post-treatment analysis.

Agalsidase beta Cardiomyopathy Enzyme replacement therapy Fabry disease Female patients Kidney function

Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
06 2020
Historique:
received: 09 09 2019
revised: 20 11 2019
accepted: 27 01 2020
pubmed: 27 2 2020
medline: 22 6 2021
entrez: 27 2 2020
Statut: ppublish

Résumé

Long-term treatment effect studies in large female Fabry patient groups are challenging to design because of phenotype heterogeneity and lack of appropriate comparison groups, and have not been reported. We compared long-term cardiomyopathy and kidney function outcomes after agalsidase beta treatment with preceding treatment-naive outcomes. Self-controlled pretreatment and post-treatment comparison (piecewise mixed linear modelling) included Fabry female patients ≥18 years at treatment initiation who received agalsidase beta (0.9-1.1 mg/kg every other week) for ≥2 years, with ≥2 pretreatment and ≥2 post-treatment outcome measurements during 10-year follow-up. Left ventricular posterior wall thickness (LVPWT)/interventricular septal thickness (IVST) and estimated glomerular filtration rate (eGFR, Chronic Kidney Disease Epidemiology Collaboration creatinine equation) analyses included 42 and 86 patients, respectively, aged 50.0 and 46.3 years at treatment initiation, respectively. LVPWT and IVST increased pretreatment (follow-up 3.5 years) but stabilized during 3.6 years of treatment (LVPWT: n = 38, slope difference [95% confidence interval (CI)] = -0.41 [-0.68, -0.15] mm/year, P Cardiac hypertrophy, progressing during pretreatment follow-up, appeared to stabilize during sustained agalsidase beta treatment. eGFR decline remained within normal ranges. This suggests that treatment may prevent further Fabry-related progression of cardiomyopathy in female patients and maintain normal kidney function.

Identifiants

pubmed: 32100468
doi: 10.1002/ehf2.12647
pmc: PMC7261571
doi:

Substances chimiques

Isoenzymes 0
alpha-Galactosidase EC 3.2.1.22
agalsidase beta RZD65TSM9U

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

825-834

Subventions

Organisme : Sanofi Genzyme
ID : -
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.

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Auteurs

Christoph Wanner (C)

Department of Medicine, Division of Nephrology, University Hospital Würzburg, Würzburg, Germany.

Ulla Feldt-Rasmussen (U)

Department of Medical Endocrinology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Ana Jovanovic (A)

The Mark Holland Unit, Department of Endocrinology and Metabolic Medicine, Salford Royal NHS Foundation Trust, Salford, UK.

Aleš Linhart (A)

2nd Department of Medicine, Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University, General University Hospital, Prague, Czech Republic.

Meng Yang (M)

Epidemiology & Biostatistics, Sanofi Genzyme, Cambridge, MA, USA.

Elvira Ponce (E)

Global Medical Affairs Rare Diseases, Sanofi Genzyme, Cambridge, MA, USA.

Eva Brand (E)

Internal Medicine D, Department of Nephrology, Hypertension and Rheumatology, University Hospital Münster, Münster, Germany.

Dominique P Germain (DP)

French Referral Center for Fabry Disease, Division of Medical Genetics and INSERM U1179, University of Versailles, Paris-Saclay University, Montigny, France.

Derralynn A Hughes (DA)

Lysosomal Storage Disorder Unit, Royal Free London NHS Foundation Trust and, University College London, London, UK.

John L Jefferies (JL)

Department of Medicine, Division of Cardiovascular Diseases, University of Tennessee Health Science Center, Memphis, TN, USA.

Ana Maria Martins (AM)

Department of Paediatrics, Federal University of São Paulo, São Paulo, Brazil.

Albina Nowak (A)

Department of Internal Medicine, University Hospital of Zürich, University of Zürich, Zürich, Switzerland.

Bojan Vujkovac (B)

Department of Internal Medicine, General Hospital Slovenj Gradec, Slovenj Gradec, Slovenia.

Frank Weidemann (F)

Medical Clinic I, Klinikum Vest, Knappschaftskrankenhaus, Recklinghausen, Germany.

Michael L West (ML)

Department of Medicine, Division of Nephrology, Dalhousie University, Halifax, Nova Scotia, Canada.

Alberto Ortiz (A)

Unidad de Dialisis, IIS-Fundación Jiménez Díaz, UAM, IRSIN, REDINREN, Madrid, Spain.

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Classifications MeSH