Agalsidase Alfa Slows the Decline in Renal Function in Patients with Fabry Disease

被引:48
作者
Feriozzi, Sandro [1 ]
Schwarting, Andreas [2 ]
Sunder-Plassmann, Gere [4 ]
West, Michael [5 ]
Cybulla, Markus [3 ]
机构
[1] Belcolle Hosp, IT-01100 Viterbo, Italy
[2] Univ Hosp, Dept Med, Mainz, Germany
[3] Univ Hosp Freiburg, Freiburg, Germany
[4] Med Univ Vienna, Div Nephrol & Dialysis, Dept Med 3, Vienna, Austria
[5] Dalhousie Univ, Dept Med, Div Nephrol, Halifax, NS, Canada
关键词
Agalsidase alfa; Enzyme replacement therapy; Fabry disease; Glomerular filtration rate; Renal function; ENZYME REPLACEMENT THERAPY; GLOMERULAR-FILTRATION-RATE; KIDNEY-DISEASE; CLINICAL-MANIFESTATIONS; SERUM CREATININE; BLOOD-PRESSURE; BETA THERAPY; PROGRESSION; SAFETY; TRIAL;
D O I
10.1159/000168482
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to determine the effects of enzyme replacement therapy with agalsidase alpha on renal function in patients with Fabry nephropathy. Serum creatinine data were collected from 165 adult patients during 3 years of treatment. Serum creatinine increased in all men whereas it was stable in women, except in stage II renal disease (Kidney Disease Outcomes Quality Initiative). The estimated glomerular filtration rate (eGFR) declined in males with stage I and II (from 115.0 +/- 22.2 to 98.3 +/- 27.3 and from 76.5 +/- 8.1 to 66.3 +/- 21.6 ml/min/1.73 m(2), respectively; both p < 0.01), whereas eGFR was stable in stage III. In females, eGFR was stable in stages I and III, and decreased in stage II (from 72.5 +/- 8.3 to 67.3 +/- 13.6 ml/min/1.73 m(2); p = 0.01). The 24-hour proteinuria was < 1 g in all patients, and most patients (96%) were treated with angiotensin receptor blockers (ARBs) or angiotensin-converting enzyme (ACE) inhibitors. Agalsidase alpha in combination with ACE inhibitors/ARB may be effective in slowing the deterioration in renal function in Fabry nephropathy. Copyright (c) 2008 S. Karger AG, Basel
引用
收藏
页码:353 / 361
页数:9
相关论文
共 31 条
[1]   Agalsidase-beta therapy for advanced Fabry disease - A randomized trial [J].
Banikazemi, Maryam ;
Bultas, Jan ;
Waldek, Stephen ;
Wilcox, William R. ;
Whitley, Chester B. ;
McDonald, Marie ;
Finkel, Richard ;
Packman, Seymour ;
Bichet, Daniel G. ;
Warnock, David G. ;
Desnick, Robert J. .
ANNALS OF INTERNAL MEDICINE, 2007, 146 (02) :77-86
[2]   ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY [J].
BRADY, RO ;
GAL, AE ;
BRADLEY, RM ;
MARTENSS.E ;
WARSHAW, AL ;
LASTER, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1967, 276 (21) :1163-&
[3]   Natural history of Fabry renal disease -: Influence of α-galactosidase A activity and genetic mutations on clinical course [J].
Branton, MH ;
Schiffmann, R ;
Sabnis, SG ;
Murray, GJ ;
Quirk, JM ;
Altarescu, G ;
Goldfarb, L ;
Brady, RO ;
Balow, JE ;
Austin, HA ;
Kopp, JB .
MEDICINE, 2002, 81 (02) :122-138
[4]   Clinical benefit of enzyme replacement therapy in Fabry disease [J].
Breunig, F ;
Weidemann, F ;
Strotmann, J ;
Knoll, A ;
Wanner, C .
KIDNEY INTERNATIONAL, 2006, 69 (07) :1216-1221
[5]  
Breunig F, 2008, J NEPHROL, V21, P32
[6]   Enzyme replacement therapy in Anderson-Fabry's disease:: beneficial clinical effect on vital organ function [J].
De Schoenmakere, G ;
Chauveau, D ;
Grünfeld, JP .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2003, 18 (01) :33-35
[7]   Safety and efficacy of recombinant human α-galactosidase a replacement therapy in Fabry's disease. [J].
Eng, CM ;
Guffon, N ;
Wilcox, WR ;
Germain, DP ;
Lee, P ;
Waldek, S ;
Caplan, L ;
Linthorst, GE ;
Desnick, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (01) :9-16
[8]   Sustained, long-term renal stabilization after 54 months of agalsidase β therapy in patients with Fabry disease [J].
Germain, Dominique P. ;
Waldek, Stephen ;
Banikazemi, Maryam ;
Bushinsky, David A. ;
Charrow, Joel ;
Desnick, Robert J. ;
Lee, Philip ;
Loew, Thomas ;
Vedder, Anouk C. ;
Abichandani, Rekha ;
Wilcox, William R. ;
Guffon, Nathalie .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2007, 18 (05) :1547-1557
[9]   A more accurate method to estimate glomerular filtration rate from serum creatinine: A new prediction equation [J].
Levey, AS ;
Bosch, JP ;
Lewis, JB ;
Greene, T ;
Rogers, N ;
Roth, D .
ANNALS OF INTERNAL MEDICINE, 1999, 130 (06) :461-+
[10]   Clinical results of enzyme replacement therapy in Fabry disease: a comprehensive review of literature [J].
Lidove, O. ;
Joly, D. ;
Barbey, F. ;
Bekri, S. ;
Alexandra, J-F ;
Peigne, V. ;
Jaussaud, R. ;
Papo, T. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2007, 61 (02) :293-302