Effectiveness of enzyme replacement therapy in Fabry disease: Long term experience in Argentina

被引:3
作者
Cabrera, Gustavo [1 ]
Politei, Juan [1 ]
Antongiovani, Norberto [1 ]
Amartino, Hernan [1 ]
机构
[1] GADYTEF, Buenos Aires, DF, Argentina
关键词
Fabry disease; Enzyme replacement therapy; Effectiveness; AGALSIDASE-BETA; NEPHROPATHY; PROGRESSION; REGISTRY; FEMALES; EVENTS; SAFETY; TRIAL; ALPHA; MALES;
D O I
10.1016/j.ymgmr.2017.02.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Evidence regarding long term effectiveness of enzyme replacement therapy (ERT) in Fabry disease (FD) is needed. The aim of this study was to analyze in a cohort of FD patients in Argentina, the long term effectiveness of ERT on renal, cardiac and cerebrovascular parameters. Methods: Patients with genetically proven FD were included from GADYTEF (Argentinean group for the treatment of FD) between 2001 and 2014. Renal, cardiac, and cerebral outcomes were prospectively studied in patients treated with ERT. Additionally, the occurrence of major cardiac complications, stroke, end-stage renal disease and death was analyzed during follow up. Results: During the follow-up 8 major complications occurred in 5 patients (n = 2 deaths, n = 4 cases of end stage renal disease and n = 1 atrial fibrillation), 4 of them males and only 1 female who suffered an atrial fibrillation. Sudden death or stroke did not occur. Four (40%) of 10 males with baseline left ventricular hypertrophy (LVH) reduced left ventricular mass index (LVMI) from 163.1 +/- 64.7 to 123.4 +/- 49.8 g/m(2), 2 stabilized LVMI and 4 increased LVMI from 157.9 +/- 32.3 to 261.6 +/- 48.6 g/m(2). Estimated glomerular filtration was stable in 30 patients (17 males and 13 females). Conclusions: We observed a few major complications during the follow up. Future studies are necessary to show the effectiveness of ERT in affected patients.
引用
收藏
页码:65 / 68
页数:4
相关论文
共 14 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]   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
[3]   Effects of enzyme replacement therapy in adult patients with Fabry disease on cardiac structure and function: a retrospective cohort study of the Fabry Munster Study (FaMuS) data [J].
Engelen, Markus A. ;
Brand, Eva ;
Baumeister, Timo B. ;
Marquardt, T. ;
Duning, Thomas ;
Osada, Nani ;
Schaefer, Roland M. ;
Stypmann, Joerg .
BMJ OPEN, 2012, 2 (06)
[4]   Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease [J].
Germain, Dominique P. ;
Charrow, Joel ;
Desnick, Robert J. ;
Guffon, Nathalie ;
Kempf, Judy ;
Lachmann, Robin H. ;
Lemay, Roberta ;
Linthorst, Gabor E. ;
Packman, Seymour ;
Scott, C. Ronald ;
Waldek, Stephen ;
Warnock, David G. ;
Weinreb, Neal J. ;
Wilcox, William R. .
JOURNAL OF MEDICAL GENETICS, 2015, 52 (05) :353-358
[5]   Recommendations for chamber quantification: A report from the American Society of Echocardiography's guidelines and standards committee and the chamber quantification writing group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology [J].
Lang, RM ;
Bierig, M ;
Devereux, RB ;
Flachskampf, FA ;
Foster, E ;
Pellikka, PA ;
Picard, MH ;
Roman, MJ ;
Seward, J ;
Shanewise, JS ;
Solomon, SD ;
Spencer, KT ;
Sutton, MS ;
Stewart, WJ .
JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY, 2005, 18 (12) :1440-1463
[6]   Nephropathy in males and females with Fabry disease: cross-sectional description of patients before treatment with enzyme replacement therapy [J].
Ortiz, Alberto ;
Oliveira, Joao P. ;
Waldek, Steven ;
Warnock, David G. ;
Cianciaruso, Bruno ;
Wanner, Christoph .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2008, 23 (05) :1600-1607
[7]   Cardiovascular Events in Patients With Fabry Disease Natural History Data From the Fabry Registry [J].
Patel, Manesh R. ;
Cecchi, Franco ;
Cizmarik, Marta ;
Kantola, Ilkka ;
Linhart, Ales ;
Nicholls, Kathy ;
Strotmann, Joerg ;
Tallaj, Jose ;
Thi Chien Tran ;
West, Michael L. ;
Beitner-Johnson, Dana ;
Abiose, Ademola .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2011, 57 (09) :1093-1099
[8]   Gastrointestinal involvement in Fabry disease. So important, yet often neglected [J].
Politei, J. ;
Thurberg, B. L. ;
Wallace, E. ;
Warnock, D. ;
Serebrinsky, G. ;
Durand, C. ;
Schenone, A. B. .
CLINICAL GENETICS, 2016, 89 (01) :5-9
[9]   Long term enzyme replacement therapy for Fabry disease: effectiveness on kidney, heart and brain [J].
Rombach, Saskia M. ;
Smid, Bouwien E. ;
Bouwman, Machtelt G. ;
Linthorst, Gabor E. ;
Dijkgraaf, Marcel G. W. ;
Hollak, Carla E. M. .
ORPHANET JOURNAL OF RARE DISEASES, 2013, 8
[10]   Enzyme replacement therapy in Fabry disease - A randomized controlled trial [J].
Schiffmann, R ;
Kopp, JB ;
Austin, HA ;
Sabnis, S ;
Moore, DF ;
Weibel, T ;
Balow, JE ;
Brady, RO .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (21) :2743-2749