Literature DB >> 30535327

Age-related renal function decline in Fabry disease patients on enzyme replacement therapy: a longitudinal cohort study.

Christoffer V Madsen1, Henrik Granqvist1, Jørgen H Petersen2, Åse K Rasmussen1, Allan M Lund3, Peter Oturai4, Søren S Sørensen5, Ulla Feldt-Rasmussen1.   

Abstract

BACKGROUND: Nephropathy is common in Fabry disease (FD). Prior studies of renal function during enzyme replacement therapy (ERT) have primarily used estimated glomerular filtration rate (eGFR). We studied the attrition of renal function in FD by measured GFR (mGFR) and urine protein excretion, and explored the influence of age.
METHODS: This was a long-term observational study of a nationwide, family-screened cohort of FD patients. All Danish genetically verified FD patients on ERT, without end-stage renal disease at baseline and with three or more mGFR values were included.
RESULTS: In all, 52 patients with consecutive mGFR values (n = 841) over median 7 years (range 1-13) were evaluated. Blood pressure remained normal and urine protein excretion was unchanged. Plasma globotriaosylceramide (Gb-3) levels normalized while plasma lyso-Gb-3 remained abnormal in 34% of patients. Baseline mGFR was 90 ± 3 mL/min/1.73 m2 and rate of renal function loss 0.9 ± 0.2 mL/min/1.73 m2/year. Baseline eGFR was 97 ± 5 mL/min/1.73 m2 and rate of renal function loss 0.8 ± 0.3 mL/min/1.73 m2/year. mGFR was age- adjusted to renal healthy non-FD subjects, giving a standard deviation score of -0.8 ± 0.2 with an annual slope of -0.03 ± 0.01 (P = 0.099), without differences between genders. Age grouping of age-adjusted data showed exaggerated renal function loss with age. Urine albumin-creatinine ratio (UACR) >300 mg/g was associated with faster renal function loss, independent of baseline mGFR, age and gender.
CONCLUSIONS: ERT-treated FD patients did not have a faster attrition of renal function than renal healthy non-FD subjects (background population). The rate of renal function loss with age was independent of gender and predicted by high UACR. We suggest cautious interpretation of non-age-adjusted FD renal data.
© The Author(s) 2018. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

Entities:  

Keywords:  Cr-EDTA; Fabry disease; age-grouping; age-standardization; albuminuria

Mesh:

Year:  2019        PMID: 30535327     DOI: 10.1093/ndt/gfy357

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  9 in total

Review 1.  Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry.

Authors:  Michael Beck; Uma Ramaswami; Elizabeth Hernberg-Ståhl; Derralynn A Hughes; Christoph Kampmann; Atul B Mehta; Kathleen Nicholls; Dau-Ming Niu; Guillem Pintos-Morell; Ricardo Reisin; Michael L West; Jörn Schenk; Christina Anagnostopoulou; Jaco Botha; Roberto Giugliani
Journal:  Orphanet J Rare Dis       Date:  2022-06-20       Impact factor: 4.303

2.  Long-term follow-up of renal function in patients treated with migalastat for Fabry disease.

Authors:  Daniel G Bichet; Roser Torra; Eric Wallace; Derralynn Hughes; Roberto Giugliani; Nina Skuban; Eva Krusinska; Ulla Feldt-Rasmussen; Raphael Schiffmann; Kathy Nicholls
Journal:  Mol Genet Metab Rep       Date:  2021-08-04

Review 3.  Clinical Characteristics, Renal Involvement, and Therapeutic Options of Pediatric Patients With Fabry Disease.

Authors:  Carmen Muntean; Iuliana Magdalena Starcea; Cristina Stoica; Claudia Banescu
Journal:  Front Pediatr       Date:  2022-06-01       Impact factor: 3.569

Review 4.  Fabry disease and kidney involvement: starting from childhood to understand the future.

Authors:  Roberto Chimenz; Valeria Chirico; Caterina Cuppari; Giorgia Ceravolo; Daniela Concolino; Paolo Monardo; Antonio Lacquaniti
Journal:  Pediatr Nephrol       Date:  2021-04-30       Impact factor: 3.651

Review 5.  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

6.  Significant hearing loss in Fabry disease: Study of the Danish nationwide cohort prior to treatment.

Authors:  Puriya Daniel Yazdanfard; Christoffer Valdorff Madsen; Lars Holme Nielsen; Åse Krogh Rasmussen; Jørgen Holm Petersen; Alka Seth; Søren Schwartz Sørensen; Lars Køber; Ulla Feldt-Rasmussen
Journal:  PLoS One       Date:  2019-12-06       Impact factor: 3.240

Review 7.  Renal Manifestations of Fabry Disease: A Narrative Review.

Authors:  Cassiano Augusto Braga Silva; José A Moura-Neto; Marlene Antônia Dos Reis; Osvaldo Merege Vieira Neto; Fellype Carvalho Barreto
Journal:  Can J Kidney Health Dis       Date:  2021-01-19

8.  Renoprotective Effect of Agalsidase Alfa: A Long-Term Follow-Up of Patients with Fabry Disease.

Authors:  Markus Cybulla; Kathleen Nicholls; Sandro Feriozzi; Aleš Linhart; Joan Torras; Bojan Vujkovac; Jaco Botha; Christina Anagnostopoulou; Michael L West
Journal:  J Clin Med       Date:  2022-08-17       Impact factor: 4.964

Review 9.  Kidney Transplant in Fabry Disease: A Revision of the Literature.

Authors:  Irene Capelli; Valeria Aiello; Lorenzo Gasperoni; Giorgia Comai; Valeria Corradetti; Matteo Ravaioli; Elena Biagini; Claudio Graziano; Gaetano La Manna
Journal:  Medicina (Kaunas)       Date:  2020-06-10       Impact factor: 2.430

  9 in total

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