Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Jan;7(1):60-9.
doi: 10.2215/CJN.03130411.

The effectiveness of long-term agalsidase alfa therapy in the treatment of Fabry nephropathy

Affiliations

The effectiveness of long-term agalsidase alfa therapy in the treatment of Fabry nephropathy

Sandro Feriozzi et al. Clin J Am Soc Nephrol. 2012 Jan.

Abstract

Background and objectives: Fabry disease is a rare X-linked disease with multisystemic manifestations. This study investigated the effectiveness of long-term enzyme replacement therapy with agalsidase alfa in Fabry nephropathy treatment.

Design, setting, participants, & measurements: In this observational study, data on patients receiving agalsidase alfa (0.2 mg/kg every other week) were extracted from the Fabry Outcome Survey, an international registry of patients with Fabry disease. Serum creatinine and estimated GFR (eGFR) at baseline and after ≥5 years of treatment were assessed; 24-hour urinary protein excretion and BP measurements were also reviewed. The eGFR was calculated using the Chronic Kidney Disease Epidemiology Collaboration formula. Patients with an eGFR <30 ml/min per 1.73 m(2) were excluded.

Results: Renal function was assessed in 208 patients (mean enzyme replacement therapy, 7.4 years; range, 5.0-11.2 years). Mean yearly change in eGFR was -2.2 ml/min per 1.73 m(2) in men and -0.7 ml/min per 1.73 m(2) in women (95% confidence limits, -2.8; -1.7 and -1.4; 0.0, respectively). Patients with 24-hour protein excretion >1 g/24 h had poorer renal function at baseline and follow-up compared with patients with protein excretion of 500-1000 mg/24 h or with proteinuria <500 mg/24 h. Renal function was worse in patients with baseline arterial hypertension, and there was a more rapid yearly decline compared with normotensive patients.

Conclusions: This study suggests that long-term agalsidase alfa therapy is able to stabilize the rate of Fabry nephropathy progression in women and is associated with a mild to moderate decline of renal function in men.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Flow chart of patient disposition. Data on creatinine concentrations at baseline and after ≥5 years of treatment were available for 208 of 1120 agalsidase alfa–treated patients. For clinical investigation, the cohort of patients was subdivided according to renal function (Kidney Disease Outcomes Quality Initiative stages), to arterial BP and to urinary protein excretion at baseline. FOS, Fabry Outcome Survey; eGFR, estimated GFR; CKD-EPI, Chronic Kidney Disease Epidemiology Collaboration.
Figure 2.
Figure 2.
Graph showing the line plots of estimated GFR (eGFR) (mean ± SD) from baseline and throughout the follow-up in patients treated with agalsidase alfa. The upper line represents male patients and the lower line represents female patients. Numbers of patients in each group are shown in parentheses.

References

    1. Ortiz A, Oliveira JP, Waldek S, Warnock DG, Cianciaruso B, Wanner C. Fabry Registry: Nephropathy in males and females with Fabry disease: Cross-sectional description of patients before treatment with enzyme replacement therapy. Nephrol Dial Transplant 23: 1600–1607, 2008 - PubMed
    1. Hughes DA, Elliott PM, Shah J, Zuckerman J, Coghlan G, Brookes J, Mehta AB: Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: A randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa. Heart 94: 153–158, 2008 - PubMed
    1. Imbriaco M, Pisani A, Spinelli L, Cuocolo A, Messalli G, Capuano E, Marmo M, Liuzzi R, Visciano B, Cianciaruso B, Salvatore M: Effects of enzyme-replacement therapy in patients with Anderson-Fabry disease: A prospective long-term cardiac magnetic resonance imaging study. Heart 95: 1103–1107, 2009 - PubMed
    1. Mehta A, Clarke JT, Giugliani R, Elliott P, Linhart A, Beck M, Sunder-Plassmann G. FOS Investigators: Natural course of Fabry disease: Changing pattern of causes of death in FOS - Fabry Outcome Survey. J Med Genet 46: 548–552, 2009 - PubMed
    1. Germain DP, Waldek S, Banikazemi M, Bushinsky DA, Charrow J, Desnick RJ, Lee P, Loew T, Vedder AC, Abichandani R, Wilcox WR, Guffon N: Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease. J Am Soc Nephrol 18: 1547–1557, 2007 - PubMed

Publication types

MeSH terms