Renal Complications of Fabry Disease

被引:1
|
作者
Basic-Jukic, Nikolina [1 ,2 ,3 ]
Kes, Petar [1 ,2 ,3 ]
Coric, Marijana [4 ]
Basic-Kes, Vanja [5 ]
机构
[1] Univ Zagreb, Sch Med, Zagreb 41001, Croatia
[2] Univ Osijek, Zagreb, Croatia
[3] Univ Hosp Ctr Zagreb, Dept Nephrol Arterial Hypertens Dialysis & Transp, Zagreb 10000, Croatia
[4] Univ Hosp Ctr Zagreb, Dept Pathol, Zagreb 10000, Croatia
[5] Univ Hosp Ctr Sisters Mercy, Dept Neurol, Zagreb, Croatia
关键词
Fabry disease; kidney; end-stage renal disease; dialysis; transplantation; enzyme replacement therapy; ENZYME REPLACEMENT THERAPY; AGALSIDASE-BETA THERAPY; ALPHA-GALACTOSIDASE; NATURAL-HISTORY; CLINICAL MANIFESTATIONS; KIDNEY; NEPHROPATHY; PROGRESSION; PREVALENCE; FEMALES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fabry disease is a progressive devastating disease caused by absent or deficient activity of lysosomal enzyme alpha-galactosidase A, with progressive accumulation of globotriaosylceramide (GL-3) within lysosomes in a different cell types. Accumulation of GL-3 and related glycosphingolipids in different cell types may create diverse clinical picture depending on the organ which is dominantly affected. Renal pathology progresses in severity with aging. Globotryaosil ceramide deposits may be found in different cell types within the kidney. Deposition within the glomeruli may be found in endothelial cells, mesangial cells, interstitial cells, with the highest level found within the podocytes. Although Fabry disease is not curable at the moment, availability of enzyme replacement therapy made it possible to treat this group of patients. Two formulations of recombinant human alpha-galactosidase A are present on the market: agalsidase alfa and agalsidase beta. Longer follow-up period is necessary to estimate the impact of ERT on mortality. Patients with end-stage renal disease caused by Fabry disease could be safely treated with enzyme replacement therapy regardless of the method of renal replacement therapy.
引用
收藏
页码:6046 / 6050
页数:5
相关论文
共 50 条
  • [1] Renal complications of Fabry disease in children
    Behzad Najafian
    Michael Mauer
    Robert J. Hopkin
    Einar Svarstad
    [J]. Pediatric Nephrology, 2013, 28 : 679 - 687
  • [2] Renal complications of Fabry disease in children
    Najafian, Behzad
    Mauer, Michael
    Hopkin, Robert J.
    Svarstad, Einar
    [J]. PEDIATRIC NEPHROLOGY, 2013, 28 (05) : 679 - 687
  • [3] Neurological complications in Fabry disease
    Duetsch, M.
    Hilz, M. J.
    [J]. REVUE DE MEDECINE INTERNE, 2010, 31 : S243 - S250
  • [4] Vascular aspects and complications in Fabry disease
    Koletzko, B
    Germain, DP
    [J]. ACTA PAEDIATRICA, 2002, 91 : 55 - 56
  • [5] Cerebrovascular complications of Fabry's disease
    Mitsias, P
    Levine, SR
    [J]. ANNALS OF NEUROLOGY, 1996, 40 (01) : 8 - 17
  • [6] NEUROLOGICAL COMPLICATIONS OF FABRY-DISEASE
    Vastagh Ildiko
    Constantin Tamas
    Keri Anna
    Rudas Gabor
    Fekete Gyoergy
    Bereczki Daniel
    [J]. IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE, 2011, 64 (1-2): : 29 - 35
  • [7] Pathomechanisms of renal Fabry disease
    Eikrem, Oystein
    Skrunes, Rannveig
    Tondel, Camilla
    Leh, Sabine
    Houge, Gunnar
    Svarstad, Einar
    Marti, Hans-Peter
    [J]. CELL AND TISSUE RESEARCH, 2017, 369 (01) : 53 - 62
  • [8] Fabry disease in a renal allograft
    Puliyanda, DP
    Wilcox, WR
    Bunnapradist, S
    Nast, CC
    Jordan, SC
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2003, 3 (08) : 1030 - 1032
  • [9] Renal pathology in Fabry disease
    Alroy, J
    Sabnis, S
    Kopp, JB
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 (06): : S134 - S138
  • [10] Renal disease in Fabry patients
    Grünfeld, JP
    Lidove, O
    Joly, D
    Barbey, F
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2001, 24 : 71 - 74