Fabry International Prognostic Index: a predictive severity score for Anderson-Fabry disease

被引:20
作者
Hughes, Derralynn A. [1 ]
Malmenas, Mia [2 ]
Deegan, Patrick B. [3 ]
Elliott, Perry M. [4 ]
Ginsberg, Lionel [1 ]
Hajioff, Daniel [5 ]
Ioannidis, Alex S. [6 ]
Orteu, Catherine H. [1 ]
Ramaswami, Uma [7 ]
West, Michael [8 ]
Pastores, Gregory M. [9 ,10 ]
Jenkinson, Crispin [11 ]
机构
[1] UCL, Lysosomal Storage Disorders Unit, Dept Haematol, London NW3 2PF, England
[2] Shire Human Genet Therapies, Global Outcome Surveys, Svardvagen Danderyd, Sweden
[3] Addenbrookes Hosp, Dept Med, Lysosmal Disorders Unit, Cambridge CB2 2QQ, England
[4] UCL, Heart Hosp, London NW3 2PF, England
[5] Univ Hosp Bristol NHS Trust, Dept Otolaryngol, Bristol, Avon, England
[6] Sydney Eye Hosp, Sydney, NSW, Australia
[7] Addenbrookes Hosp, Paediat Metab Unit, Cambridge, England
[8] Dalhousie Univ, Dept Med, Div Nephrol, Halifax, NS, Canada
[9] NYU, Dept Neurol, Sch Med, New York, NY 10016 USA
[10] NYU, Sch Med, Dept Paediat, New York, NY USA
[11] Univ Oxford, Dept Publ Hlth, Oxford, England
关键词
ENZYME REPLACEMENT THERAPY; OUTCOME SURVEY; CLINICAL-MANIFESTATIONS; NATURAL-HISTORY; SYSTEM; FEMALES; TRIAL;
D O I
10.1136/jmedgenet-2011-100407
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Anderson-Fabry disease (AFD) is a disorder of glycosphingolipid metabolism resulting from deficiency of a-galactosidase A and accumulation of globotriaosylceramide. Presentation is heterogeneous and, despite guidelines for initiation of therapy, there is no basis for defining subgroups that will progress more rapidly, whether treated or not. The authors of this study used clinical and pathological data recorded on 1483 patients in the Fabry Outcome Survey, a large international registry, to develop a prognostic severity score. Methods Parameters relevant to disease progression or outcome were initially selected, using variables that are readily available in clinical practice. Individual end points for renal, cardiac, neurological disease, and death were selected, and a composite end point developed. Potential prognostic variables were correlated with each end point, before multivariate analysis. Variables retaining significance were then used to construct organ specific and composite prognostic scores. Kaplan-Meier (KM) analysis, according to score, was performed for each end point. Results Analysis demonstrated that it is possible to differentiate groups of patients with different outcome probabilities. Cardiac, renal and neurological end points could each be categorised into three separate groups. The 80% event-free survival for these groups differed by approximately 10 years. The overall composite score, the Fabry International Prognostic Index (FIPI), distinguished two distinct groups where the 50% event-free survival differed by 10 years. Conclusions A prognostic scoring system for AFD has been developed and retrospective validation performed. The FIPI should prove to be a valuable tool in the counselling and management of AFD patients, and in comparative analyses of outcome using different therapies.
引用
收藏
页码:212 / 220
页数:9
相关论文
共 21 条
[1]   Does geographical location influence the phenotype of Fabry disease in women in Europe? [J].
Barba-Romero, M-A ;
Deegan, P. ;
Giugliani, R. ;
Hughes, D. .
CLINICAL GENETICS, 2010, 77 (02) :131-140
[2]   The Mainz Severity Score Index (MSSI): development and validation of a system for scoring the signs and symptoms of Fabry disease [J].
Beck, M .
ACTA PAEDIATRICA, 2006, 95 :43-46
[3]   Natural history of Fabry disease in females in the Fabry outcome survey [J].
Deegan, PB ;
Baehner, AF ;
Romero, MAB ;
Hughes, DA ;
Kampmann, C ;
Beck, M .
JOURNAL OF MEDICAL GENETICS, 2006, 43 (04) :347-352
[4]   ECHOCARDIOGRAPHIC ASSESSMENT OF LEFT-VENTRICULAR HYPERTROPHY - COMPARISON TO NECROPSY FINDINGS [J].
DEVEREUX, RB ;
ALONSO, DR ;
LUTAS, EM ;
GOTTLIEB, GJ ;
CAMPO, E ;
SACHS, I ;
REICHEK, N .
AMERICAN JOURNAL OF CARDIOLOGY, 1986, 57 (06) :450-458
[5]   Fabry disease: Guidelines for the evaluation and management of multi-organ system involvement [J].
Eng, Christine M. ;
Germain, Dominique P. ;
Banikazemi, Maryam ;
Warnock, David G. ;
Wanner, Christoph ;
Hopkin, Robert J. ;
Bultas, Jan ;
Lee, Philip ;
Sims, Katherine ;
Brodie, Scott E. ;
Pastores, Gregory M. ;
Strotmann, Joerg M. ;
Wilcox, William R. .
GENETICS IN MEDICINE, 2006, 8 (09) :539-548
[6]   A phase 1/2 clinical trial of enzyme replacement in Fabry disease: Pharmacokinetic, substrate clearance, and safety studies [J].
Eng, CM ;
Banikazemi, M ;
Gordon, RE ;
Goldman, M ;
Phelps, R ;
Kim, L ;
Gass, A ;
Winston, J ;
Dikman, S ;
Fallon, JT ;
Brodie, S ;
Stacy, CB ;
Mehta, D ;
Parsons, R ;
Norton, K ;
O'Callaghan, M ;
Desnick, RJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :711-722
[7]   A validated disease severity scoring system for Fabry disease [J].
Giannini, Edward H. ;
Mehta, Atul B. ;
Hilz, Max J. ;
Beck, Michael ;
Bichet, Daniel G. ;
Brady, Roscoe O. ;
West, Michael ;
Germain, Dominique P. ;
Wanner, Christoph ;
Waldek, Stephen ;
Clarke, Joe T. R. ;
Mengel, Eugen ;
Strotmann, Joerg M. ;
Warnock, David G. ;
Linhart, Ales .
MOLECULAR GENETICS AND METABOLISM, 2010, 99 (03) :283-290
[8]   The use of scoring systems in patients with haematological malignancy [J].
Hughes, Derralynn A. .
ACTA PAEDIATRICA, 2006, 95 :47-51
[9]  
KINT J A, 1970, Science (Washington D C), V167, P1268, DOI 10.1126/science.167.3922.1268
[10]   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-+