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Volumn 26, Issue 4, 2013, Pages 645-651

Kidney transplantation and enzyme replacement therapy in patients with Fabry disease

Author keywords

Agalsidase alfa; Agalsidase beta; End stage renal disease (ESRD); Enzyme replacement therapy (ERT); Fabry disease; Kidney transplantation; Nephropathy

Indexed keywords

AGALSIDASE ALFA; AGALSIDASE BETA; ALPHA GALACTOSIDASE; CREATININE; GLOBOTRIAOSYLCERAMIDE; GLYCOSPHINGOLIPID; IMMUNOSUPPRESSIVE AGENT;

EID: 84880089118     PISSN: 11218428     EISSN: 17246059     Source Type: Journal    
DOI: 10.5301/jn.5000214     Document Type: Review
Times cited : (16)

References (40)
  • 1
    • 0036234750 scopus 로고    scopus 로고
    • Advances in the management of Anderson-Fabry disease: Enzyme replacement therapy
    • Pastores GM, Thadhani R. Advances in the management of Anderson-Fabry disease: enzyme replacement therapy. Expert Opin Biol Ther. 2002;2(3):325-333.
    • (2002) Expert Opin Biol Ther , vol.2 , Issue.3 , pp. 325-333
    • Pastores, G.M.1    Thadhani, R.2
  • 2
    • 26944497278 scopus 로고    scopus 로고
    • Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneys
    • Cybulla M, Schaefer E, Wendt S, et al. Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneys. Am J Kidney Dis. 2005;45(5): e82-e89.
    • (2005) Am J Kidney Dis , vol.45 , Issue.5
    • Cybulla, M.1    Schaefer, E.2    Wendt, S.3
  • 3
    • 0034754467 scopus 로고    scopus 로고
    • Anderson-Fabry disease: Clinical manifestations and impact of disease in a cohort of 60 obligate carrier females
    • MacDermot KD, Holmes A, Miners AH. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. J Med Genet. 2001; 38(11):769-775.
    • (2001) J Med Genet , vol.38 , Issue.11 , pp. 769-775
    • Macdermot, K.D.1    Holmes, A.2    Miners, A.H.3
  • 4
    • 0035157764 scopus 로고    scopus 로고
    • Natural history of Fabry disease in affected males and obligate carrier females
    • discussion 11-12
    • MacDermot KD, Holmes A, Miners AH. Natural history of Fabry disease in affected males and obligate carrier females. J Inherit Metab Dis. 2001; 24 2 (Suppl 2):13-14 discussion 11-12.
    • (2001) J Inherit Metab Dis , vol.24 , Issue.2 SUPPL. 2 , pp. 13-14
    • Macdermot, K.D.1    Holmes, A.2    Miners, A.H.3
  • 5
    • 34447607076 scopus 로고
    • Ein Beitrag zur Kenntnis der Purpura haemorrhagica nodularis (Purpura papulosa hemorrhagica Hebrae)
    • Fabry J. Ein Beitrag zur Kenntnis der Purpura haemorrhagica nodularis (Purpura papulosa hemorrhagica Hebrae). Arch Derm Syphilol. 1898;43:187-200.
    • (1898) Arch Derm Syphilol , vol.43 , pp. 187-200
    • Fabry, J.1
  • 6
    • 84980085880 scopus 로고
    • A case of angio-keratoma
    • Anderson W. A case of "angio-keratoma". Br J Dermatol. 1898;10(4):113-117.
    • (1898) Br J Dermatol , vol.10 , Issue.4 , pp. 113-117
    • Anderson, W.1
  • 7
    • 0036260287 scopus 로고    scopus 로고
    • Anderson-Fabry disease: Its place among other genetic causes of renal disease
    • Grünfeld JP, Chauveau D, Lévy M. Anderson-Fabry disease: its place among other genetic causes of renal disease. J Am Soc Nephrol. 2002;13(Suppl 2):S126-S129.
    • (2002) J Am Soc Nephrol , vol.13 , Issue.SUPPL. 2
    • Grünfeld, J.P.1    Chauveau, D.2    Lévy, M.3
  • 8
    • 0017872842 scopus 로고
    • Early renal changes in hemizygous and heterozygous patients with Fabry's disease
    • Gubler MC, Lenoir G, Grünfeld JP, et al. Early renal changes in hemizygous and heterozygous patients with Fabry's disease. Kidney Int. 1978;13(3):223-235.
    • (1978) Kidney Int , vol.13 , Issue.3 , pp. 223-235
    • Gubler, M.C.1    Lenoir, G.2    Grünfeld, J.P.3
  • 9
    • 0036266877 scopus 로고    scopus 로고
    • Natural history and treatment of renal involvement in Fabry disease
    • Branton M, Schiffmann R, Kopp JB. Natural history and treatment of renal involvement in Fabry disease. J Am Soc Nephrol. 2002;13(Suppl 2):S139-S143.
    • (2002) J Am Soc Nephrol , vol.13 , Issue.SUPPL. 2
    • Branton, M.1    Schiffmann, R.2    Kopp, J.B.3
  • 10
    • 54949106603 scopus 로고    scopus 로고
    • International Fabry Outcome Survey Investigators. Agalsidase alfa slows the decline in renal function in patients with Fabry disease
    • Feriozzi S, Schwarting A, Sunder-Plassmann G, West M, Cybulla M; International Fabry Outcome Survey Investigators. Agalsidase alfa slows the decline in renal function in patients with Fabry disease. Am J Nephrol. 2009;29(5):353-361.
    • (2009) Am J Nephrol , vol.29 , Issue.5 , pp. 353-361
    • Feriozzi, S.1    Schwarting, A.2    Sunder-Plassmann, G.3    West, M.4    Cybulla, M.5
  • 11
    • 0035157578 scopus 로고    scopus 로고
    • Renal pathological changes in Fabry disease
    • discussion 65
    • Sessa A, Meroni M, Battini G, et al. Renal pathological changes in Fabry disease. J Inherit Metab Dis. 2001;24 2 Suppl 2:66-70, discussion 65.
    • (2001) J Inherit Metab Dis , vol.24 , Issue.2 SUPPL. 2 , pp. 66-70
    • Sessa, A.1    Meroni, M.2    Battini, G.3
  • 12
    • 0036436320 scopus 로고    scopus 로고
    • Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy
    • Thurberg BL, Rennke H, Colvin RB, et al. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy. Kidney Int. 2002;62(6):1933-1946.
    • (2002) Kidney Int , vol.62 , Issue.6 , pp. 1933-1946
    • Thurberg, B.L.1    Rennke, H.2    Colvin, R.B.3
  • 13
    • 43049092306 scopus 로고    scopus 로고
    • Renal biopsy findings in children and adolescents with Fabry disease and minimal albuminuria
    • Tøndel C, Bostad L, Hirth A, Svarstad E. Renal biopsy findings in children and adolescents with Fabry disease and minimal albuminuria. Am J Kidney Dis. 2008;51(5):767-776.
    • (2008) Am J Kidney Dis , vol.51 , Issue.5 , pp. 767-776
    • Tøndel, C.1    Bostad, L.2    Hirth, A.3    Svarstad, E.4
  • 14
    • 52649095922 scopus 로고    scopus 로고
    • Kidney biopsy findings in heterozygous Fabry disease females with early nephropathy
    • Valbuena C, Carvalho E, Bustorff M, et al. Kidney biopsy findings in heterozygous Fabry disease females with early nephropathy. Virchows Arch. 2008;453(4):329-338.
    • (2008) Virchows Arch , vol.453 , Issue.4 , pp. 329-338
    • Valbuena, C.1    Carvalho, E.2    Bustorff, M.3
  • 15
    • 0036122659 scopus 로고    scopus 로고
    • Natural history of Fabry renal disease: Influence of alpha-galactosidase A activity and genetic mutations on clinical course
    • Branton MH, Schiffmann R, Sabnis SG, et al. Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course. Medicine (Baltimore). 2002;81(2):122-138.
    • (2002) Medicine (Baltimore) , vol.81 , Issue.2 , pp. 122-138
    • Branton, M.H.1    Schiffmann, R.2    Sabnis, S.G.3
  • 16
    • 0036263495 scopus 로고    scopus 로고
    • Renal pathology in Fabry disease
    • Alroy J, Sabnis S, Kopp JB. Renal pathology in Fabry disease. J Am Soc Nephrol. 2002;13(Suppl 2):S134-S138.
    • (2002) J Am Soc Nephrol , vol.13 , Issue.SUPPL. 2
    • Alroy, J.1    Sabnis, S.2    Kopp, J.B.3
  • 17
    • 77954321307 scopus 로고    scopus 로고
    • All members of the International Study Group of Fabry Nephropathy (ISGFN)
    • Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN)
    • Fogo AB, Bostad L, Svarstad E, et al. All members of the International Study Group of Fabry Nephropathy (ISGFN). Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN). Nephrol Dial Transplant. 2010;25(7):2168-2177.
    • (2010) Nephrol Dial Transplant , vol.25 , Issue.7 , pp. 2168-2177
    • Fogo, A.B.1    Bostad, L.2    Svarstad, E.3
  • 18
    • 79952192786 scopus 로고    scopus 로고
    • Progressive podocyte injury and globotriaosylceramide (GL-3) accumulation in young patients with Fabry disease
    • Najafian B, Svarstad E, Bostad L, et al. Progressive podocyte injury and globotriaosylceramide (GL-3) accumulation in young patients with Fabry disease. Kidney Int. 2011; 79(6):663-670.
    • (2011) Kidney Int , vol.79 , Issue.6 , pp. 663-670
    • Najafian, B.1    Svarstad, E.2    Bostad, L.3
  • 19
    • 67651123138 scopus 로고    scopus 로고
    • Fabry disease: Progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy
    • Schiffmann R, Warnock DG, Banikazemi M, et al. Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy. Nephrol Dial Transplant. 2009;24(7):2102-2111.
    • (2009) Nephrol Dial Transplant , vol.24 , Issue.7 , pp. 2102-2111
    • Schiffmann, R.1    Warnock, D.G.2    Banikazemi, M.3
  • 20
    • 44449143398 scopus 로고    scopus 로고
    • Fabry Registry. Nephropathy in males and females with Fabry disease: Cross-sectional description of patients before treatment with enzyme replacement therapy
    • 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. 2008;23(5):1600-1607.
    • (2008) Nephrol Dial Transplant , vol.23 , Issue.5 , pp. 1600-1607
    • Ortiz, A.1    Oliveira, J.P.2    Waldek, S.3    Warnock, D.G.4    Cianciaruso, B.5    Wanner, C.6
  • 22
    • 0034660663 scopus 로고    scopus 로고
    • Excellent outcome of renal transplantation in patients with Fabry's disease
    • Ojo A, Meier-Kriesche HU, Friedman G, et al. Excellent outcome of renal transplantation in patients with Fabry's disease. Transplantation. 2000;69(11):2337-2339.
    • (2000) Transplantation , vol.69 , Issue.11 , pp. 2337-2339
    • Ojo, A.1    Meier-Kriesche, H.U.2    Friedman, G.3
  • 23
    • 12644253826 scopus 로고    scopus 로고
    • Report on management of renale failure in Europe, XXVI, 1995. Rare diseases in renal replacement therapy in the ERA-EDTA Registry
    • Tsakiris D, Simpson HK, Jones EH, et al. Report on management of renale failure in Europe, XXVI, 1995. Rare diseases in renal replacement therapy in the ERA-EDTA Registry. Nephrol Dial Transplant. 1996;11(Suppl 7):4-20.
    • (1996) Nephrol Dial Transplant , vol.11 , Issue.SUPPL. 7 , pp. 4-20
    • Tsakiris, D.1    Simpson, H.K.2    Jones, E.H.3
  • 24
    • 0024467601 scopus 로고
    • Outcome of end-stage renal disease in patients with rare causes of renal failure. I. Inherited and metabolic disorders
    • Nissenson AR, Port FK. Outcome of end-stage renal disease in patients with rare causes of renal failure. I. Inherited and metabolic disorders. Q J Med. 1989;73(271):1055-1062.
    • (1989) Q J Med , vol.73 , Issue.271 , pp. 1055-1062
    • Nissenson, A.R.1    Port, F.K.2
  • 25
    • 0021592719 scopus 로고
    • Transplantation in relation to the treatment of inherited disease
    • Groth CG, Ringdén O. Transplantation in relation to the treatment of inherited disease. Transplantation. 1984;38(4): 319-327.
    • (1984) Transplantation , vol.38 , Issue.4 , pp. 319-327
    • Groth, C.G.1    Ringdén, O.2
  • 26
    • 0028298684 scopus 로고
    • Recurrent diseases in the kidney transplant
    • Ramos EL, Tisher CC. Recurrent diseases in the kidney transplant. Am J Kidney Dis. 1994;24(1):142-154.
    • (1994) Am J Kidney Dis , vol.24 , Issue.1 , pp. 142-154
    • Ramos, E.L.1    Tisher, C.C.2
  • 28
    • 0016802543 scopus 로고
    • Renal transplantation in patients suffering from Fabry's disease. Kidney transplantation from an heterozygote subject to a subject without Fabry's disease
    • Grünfeld JP, Le Porrier M, Droz D, Bensaude I, Hinglais N, Crosnier J. [Renal transplantation in patients suffering from Fabry's disease. Kidney transplantation from an heterozygote subject to a subject without Fabry's disease]. Nouv Presse Med. 1975;4(29):2081-2085.
    • (1975) Nouv Presse Med , vol.4 , Issue.29 , pp. 2081-2085
    • Grünfeld, J.P.1    Le Porrier, M.2    Droz, D.3    Bensaude, I.4    Hinglais, N.5    Crosnier, J.6
  • 29
    • 0023079624 scopus 로고
    • Involvement of renal allograft by Fabry's disease
    • Popli S, Molnar ZV, Leehey DJ, et al. Involvement of renal allograft by Fabry's disease. Am J Nephrol. 1987;7(4):316-318.
    • (1987) Am J Nephrol , vol.7 , Issue.4 , pp. 316-318
    • Popli, S.1    Molnar, Z.V.2    Leehey, D.J.3
  • 32
    • 59249084843 scopus 로고    scopus 로고
    • Anderson-Fabry disease: A case-finding study among male kidney transplant recipients in Austria
    • Kleinert J, Kotanko P, Spada M, et al. Anderson-Fabry disease: a case-finding study among male kidney transplant recipients in Austria. Transpl Int. 2009;22(3):287-292.
    • (2009) Transpl Int , vol.22 , Issue.3 , pp. 287-292
    • Kleinert, J.1    Kotanko, P.2    Spada, M.3
  • 33
    • 29544435188 scopus 로고    scopus 로고
    • Kidney transplantation improves survival and is indicated in Fabry's disease
    • Inderbitzin D, Avital I, Largiadèr F, Vogt B, Candinas D. Kidney transplantation improves survival and is indicated in Fabry's disease. Transplant Proc. 2005;37(10):4211-4214.
    • (2005) Transplant Proc , vol.37 , Issue.10 , pp. 4211-4214
    • Inderbitzin, D.1    Avital, I.2    Largiadèr, F.3    Vogt, B.4    Candinas, D.5
  • 34
    • 39749149610 scopus 로고    scopus 로고
    • Fabry nephropathy: 5 years of enzyme replacement therapy-a short review
    • Barbey F, Lidove O, Schwarting A. Fabry nephropathy: 5 years of enzyme replacement therapy-a short review. NDT Plus. 2008;1(1):11-19.
    • (2008) NDT Plus , vol.1 , Issue.1 , pp. 11-19
    • Barbey, F.1    Lidove, O.2    Schwarting, A.3
  • 35
    • 77749325037 scopus 로고    scopus 로고
    • Dialysis and transplantation in Fabry disease: Indications for enzyme replacement therapy
    • Mignani R, Feriozzi S, Schaefer RM, et al. Dialysis and transplantation in Fabry disease: indications for enzyme replacement therapy. Clin J Am Soc Nephrol. 2010;5(2):379-385.
    • (2010) Clin J Am Soc Nephrol , vol.5 , Issue.2 , pp. 379-385
    • Mignani, R.1    Feriozzi, S.2    Schaefer, R.M.3
  • 36
    • 65649096032 scopus 로고    scopus 로고
    • Agalsidase alfa and kidney dysfunction in Fabry disease
    • West M, Nicholls K, Mehta A, et al. Agalsidase alfa and kidney dysfunction in Fabry disease. J Am Soc Nephrol. 2009; 20(5):1132-1139.
    • (2009) J Am Soc Nephrol , vol.20 , Issue.5 , pp. 1132-1139
    • West, M.1    Nicholls, K.2    Mehta, A.3
  • 37
    • 1642463470 scopus 로고    scopus 로고
    • Enzyme replacement therapy with agalsidase beta in kidney transplant patients with Fabry disease: A pilot study
    • Mignani R, Panichi V, Giudicissi A, et al. Enzyme replacement therapy with agalsidase beta in kidney transplant patients with Fabry disease: a pilot study. Kidney Int. 2004;65(4): 1381-1385.
    • (2004) Kidney Int , vol.65 , Issue.4 , pp. 1381-1385
    • Mignani, R.1    Panichi, V.2    Giudicissi, A.3
  • 38
    • 34547830275 scopus 로고    scopus 로고
    • Safety and pharmacokinetics of agalsidase alfa in patients with Fabry disease and end-stage renal disease
    • Pastores GM, Boyd E, Crandall K, Whelan A, Piersall L, Barnett N. Safety and pharmacokinetics of agalsidase alfa in patients with Fabry disease and end-stage renal disease. Nephrol Dial Transplant. 2007;22(7):1920-1925.
    • (2007) Nephrol Dial Transplant , vol.22 , Issue.7 , pp. 1920-1925
    • Pastores, G.M.1    Boyd, E.2    Crandall, K.3    Whelan, A.4    Piersall, L.5    Barnett, N.6
  • 39
    • 44449157135 scopus 로고    scopus 로고
    • Agalsidase therapy in patients with Fabry disease on renal replacement therapy: A nationwide study in Italy
    • Mignani R, Feriozzi S, Pisani A, et al. Agalsidase therapy in patients with Fabry disease on renal replacement therapy: a nationwide study in Italy. Nephrol Dial Transplant. 2008; 23(5):1628-1635.
    • (2008) Nephrol Dial Transplant , vol.23 , Issue.5 , pp. 1628-1635
    • Mignani, R.1    Feriozzi, S.2    Pisani, A.3


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