End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry

被引:89
|
作者
Ortiz, Alberto [1 ]
Cianciaruso, Bruno [2 ]
Cizmarik, Marta [3 ]
Germain, Dominique P. [4 ]
Mignani, Renzo [5 ]
Oliveira, Joao Paulo [6 ,7 ]
Villalobos, Jacobo [8 ]
Vujkovac, Bojan [9 ]
Waldek, Stephen [10 ]
Wanner, Christoph [11 ]
Warnock, David G. [12 ]
机构
[1] Univ Autonoma Madrid, Fdn Jimenez Diaz, Unidad Dialisis, Madrid, Spain
[2] Univ Naples Federico II, Dept Nephrol, Naples, Italy
[3] Genzyme Corp, Cambridge, MA USA
[4] Univ Versailles St Quentin Yvelines, Hop Raymond Poincare, Garches, France
[5] Infermi Hosp, Dept Nephrol & Dialysis, Rimini, Italy
[6] Hosp Sao Joao, Fac Med, Dept Nephrol, Oporto, Portugal
[7] Hosp Sao Joao, Fac Med, Dept Human Genet, Oporto, Portugal
[8] Cent Univ Venezuela, Luis Razetti Sch Med, Dept Physiol, Caracas, Venezuela
[9] Gen Hosp Slovenj Gradec, Dept Internal Med, Slovenj Gradec, Slovenia
[10] Salford Royal NHS Fdn Trust, Salford M6 8HD, Lancs, England
[11] Univ Wurzburg, Div Nephrol, Dept Med, Wurzburg, Germany
[12] Univ Alabama Birmingham, Div Nephrol, Birmingham, AL USA
关键词
chronic kidney disease; Fabry disease; genetic renal disease; kidney transplantation; ENZYME REPLACEMENT THERAPY; GLOMERULAR-FILTRATION-RATE; AGALSIDASE-BETA THERAPY; ALPHA-GALACTOSIDASE; NEPHROPATHY; CREATININE; MUTATIONS; FEMALES; EVENTS; TRIAL;
D O I
10.1093/ndt/gfp554
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Methods. Data from 2712 patients in the Fabry Registry were analysed to identify clinical characteristics of patients who received renal replacement therapy (RRT) during the natural history period (i.e. prior to any enzyme replacement therapy). Results. A total of 213 patients [186 of 1359 males (14%) and 27 of 1353 females (2%)] received RRT at a median age of 38 years in both males and females. Males who received RRT were diagnosed at a median age of 35 years, compared to 23 years for non-RRT males. Sixty-one males and 10 females were not diagnosed with Fabry disease until after they had received RRT. Compared to other Fabry Registry patients, a higher percentage of RRT patients also experienced either a serious cardiovascular event or a stroke. Ninety-two of 186 males who had RRT (50%) experienced a cardiac event or stroke, compared to 230 of 1173 non-RRT males (20%). Ten of 27 RRT females (37%) had experienced a cardiac event or stroke, compared to 226 of 1326 non-RRT females (17%). Patients who had RRT experienced cardiovascular events and strokes at earlier ages than did patients who had not received RRT, and most received RRT before having a cardiac event or stroke. Conclusions. While all Fabry patients are at risk of cardiovascular events and strokes, patients with Fabry nephropathy who develop kidney failure appear to have concurrent involvement of other major organ systems. It is important that Fabry patients are diagnosed early and that their renal function is monitored carefully.
引用
收藏
页码:769 / 775
页数:7
相关论文
共 50 条
  • [21] Screening of Fabry disease in patients with end-stage renal disease of unknown etiology:the first Thailand study
    Objoon Trachoo
    Paisan Jittorntam
    Sarunpong Pibalyart
    Saowanee Kajanachumphol
    Norasak Suvachittanont
    Suthep Patputthipong
    Piyatida Chuengsaman
    Arkom Nongnuch
    [J]. The Journal of Biomedical Research, 2017, 31 (01) : 17 - 24
  • [22] Atypical variant and an indirect diagnosis of Fabry disease in a patient with end-stage renal disease
    Ciabattini, F.
    Bordoni, E.
    Guerrini, E.
    Scarfone, V.
    [J]. CLINICAL THERAPEUTICS, 2007, 29 : S26 - S27
  • [23] Fabry disease: Delineating the natural history of the disorder through the Fabry Registry.
    Eng, CM
    Banikazemi, M
    Barranger, J
    Charrow, J
    Clark, L
    Bushinsky, D
    Hopkin, R
    Pastores, G
    Scott, CR
    Sims, K
    Wilcox, W
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 453 - 453
  • [24] FAMILY SCREENING FOR FABRY DISEASE BASED ON MALE INDEX CASES WITH END-STAGE RENAL DISEASE
    Silva, Cassiano A. B.
    Moura Junior, Jose A.
    Cruz, Constanca M. S.
    Barreto, Fellype C.
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 : 357 - 357
  • [25] STROKES IN PATIENTS WITH FABRY DISEASE FREQUENTLY OCCUR BEFORE DIAGNOSIS AND IN THE ABSENCE OF OTHER CLINICAL EVENTS: NATURAL HISTORY DATA FROM THE FABRY REGISTRY
    Sims, K.
    Poleitei, J.
    Banikazemi, M.
    Lee, P.
    [J]. CLINICAL THERAPEUTICS, 2008, 30 : S105 - S105
  • [26] Novel frameshift mutation in a heterozygous woman with Fabry disease and end-stage renal failure
    VanLoo, A
    Vanholder, R
    Madsen, K
    Praet, M
    Kint, J
    DePaepe, A
    Messiaen, L
    Lameire, N
    Hasholt, L
    Sorensen, SA
    Ringoir, S
    [J]. AMERICAN JOURNAL OF NEPHROLOGY, 1996, 16 (04) : 352 - 357
  • [27] Left ventricular hypertrophy and end-stage renal failure of unknown etiology: Fabry disease?
    Arevalo-Gomez, A.
    Rivera-Garcia, S.
    Lopez-Muniz, A.
    Barriales-Villa, R.
    [J]. REVISTA CLINICA ESPANOLA, 2012, 212 (05): : 265 - 266
  • [28] The Natural History of Fabry Disease
    Warnock, David G.
    [J]. CLINICAL THERAPEUTICS, 2010, 32 : S101 - S102
  • [29] Natural history and treatment of renal involvement in Fabry disease
    Branton, M
    Schiffmann, R
    Kopp, JB
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 (06): : S139 - S143
  • [30] CLINICAL PROFILE OF BRAZILIAN PATIENTS WITH FABRY DISEASE (FD): DATA FROM BRAZILIAN FABRY REGISTRY
    Martins, A. M.
    Kyosen, S. O.
    Micheletti, C.
    Mendes, C. S. C.
    Gomes, J. G.
    Norato, D.
    Sobral Neto, J.
    Biagini, G.
    Azevedo, D. J.
    Aranda, P. C.
    Sousa, A. F.
    Bastos, R., V
    Chamoles, N. A.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 : 163 - 163