A 15-Year Perspective of the Fabry Outcome Survey:

The Fabry Outcome Survey (FOS) is an international long-term observational registry sponsored by Shire for patients diagnosed with Fabry disease who are receiving or are candidates for therapy with agalsidase alfa (agalα). Established in 2001, FOS provides long-term data on agalα safety/efficacy and collects data on the natural history of Fabry disease, with the aim of improving clinical management. The FOS publications have helped establish prognostic and severity scores, defined the incidence of specific disease variants and implications for clinical management, described clinical manifestations in special populations, confirmed the high prevalence of cardiac morbidity, and demonstrated correlations between ocular changes and Fabry disease severity. These FOS data represent a rich resource with utility not only for description of natural history/therapeutic effects but also for exploratory hypothesis testing and generation of tools for diagnosis/management, with the potential to improve future patient o...

[1]  C. Hollak,et al.  Response of women with Fabry disease to enzyme replacement therapy: comparison with men, using data from FOS--the Fabry Outcome Survey. , 2011, Molecular genetics and metabolism.

[2]  A. Schwarting,et al.  The Mainz Severity Score Index: a new instrument for quantifying the Anderson–Fabry disease phenotype, and the response of patients to enzyme replacement therapy , 2004, Clinical genetics.

[3]  R. Artuch,et al.  Fabry disease in Spain: description of Spanish patients and a comparison with other European countries using data from the Fabry Outcome Survey (FOS) , 2011, International journal of clinical practice.

[4]  R. Giugliani,et al.  Does geographical location influence the phenotype of Fabry disease in women in Europe? , 2010, Clinical genetics.

[5]  J. Zamorano,et al.  Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome survey. , 2007, European heart journal.

[6]  Wen-Chung Yu,et al.  Age at First Cardiac Symptoms in Fabry Disease: Association with a Chinese Hotspot Fabry Mutation (IVS4+919G>A), Classical Fabry Mutations, and Sex in a Taiwanese Population from the Fabry Outcome Survey (FOS). , 2015, JIMD reports.

[7]  Atul Mehta,et al.  Nature and Prevalence of Pain in Fabry Disease and Its Response to Enzyme Replacement Therapy—A Retrospective Analysis From the Fabry Outcome Survey , 2007, The Clinical journal of pain.

[8]  K. Macdermot,et al.  Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females , 2001, Journal of medical genetics.

[9]  S. Keshav,et al.  Gastrointestinal symptoms in Fabry disease: everything is possible, including treatment , 2007, Acta paediatrica.

[10]  M. Gladwin,et al.  Regional Cerebral Hyperperfusion and Nitric Oxide Pathway Dysregulation in Fabry Disease: Reversal by Enzyme Replacement Therapy , 2001, Circulation.

[11]  R. Schiffmann,et al.  Elevated Cerebral Blood Flow Velocities in Fabry Disease With Reversal After Enzyme Replacement , 2002, Stroke.

[12]  A. Rolfs,et al.  [Fabry disease: demographic data since introduction of enzyme replacement therapy]. , 2007, Deutsche medizinische Wochenschrift.

[13]  U. Ramaswami,et al.  Fabry disease in children and response to enzyme replacement therapy: results from the Fabry Outcome Survey , 2012, Clinical genetics.

[14]  Thomas P. Mechtler,et al.  Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria , 2012, The Lancet.

[15]  B. Kendall,et al.  Magnetic resonance imaging changes in Fabry disease. , 2006, Acta paediatrica (Oslo, Norway : 1992). Supplement.

[16]  S. Oparil,et al.  Prevalence of apparent treatment-resistant hypertension among individuals with CKD. , 2013, Clinical journal of the American Society of Nephrology : CJASN.

[17]  C. Renier,et al.  Effect of angiotensin converting enzyme inhibitors and angiotensin receptor blockers on hemoglobin levels , 2013, BMC Research Notes.

[18]  W. Rand,et al.  Reduced kidney function and anemia as risk factors for mortality in patients with left ventricular dysfunction. , 2001, Journal of the American College of Cardiology.

[19]  G. Houge,et al.  Anemia is a new complication in Fabry disease: data from the Fabry Outcome Survey. , 2005, Kidney international.

[20]  K. Nicholls,et al.  Cardiovascular outcomes in Fabry disease are linked to severity of chronic kidney disease , 2014, Heart.

[21]  V. Vaccarino,et al.  Chronic kidney disease, anemia, and incident stroke in a middle-aged, community-based population: the ARIC Study. , 2003, Kidney international.

[22]  S. Feriozzi,et al.  Agalsidase Alfa Slows the Decline in Renal Function in Patients with Fabry Disease , 2008, American Journal of Nephrology.

[23]  G. Bakris,et al.  The double challenge of resistant hypertension and chronic kidney disease , 2015, The Lancet.

[24]  G. Houge,et al.  Prevalence of uncontrolled hypertension in patients with Fabry disease. , 2006, American journal of hypertension.

[25]  R. Schiffmann,et al.  Agalsidase alfa and kidney dysfunction in Fabry disease. , 2009, Journal of the American Society of Nephrology : JASN.

[26]  A. Gal,et al.  A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry disease , 2009, Genetics in Medicine.

[27]  R. Minutolo,et al.  Prevalence and prognostic role of resistant hypertension in chronic kidney disease patients. , 2013, Journal of the American College of Cardiology.

[28]  W. Hörl,et al.  Effect of erythropoietin on cardiovascular diseases. , 2001, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[29]  C. Whybra,et al.  Measurement of disease severity and progression in Fabry disease , 2006 .

[30]  R. Desnick,et al.  High incidence of later-onset fabry disease revealed by newborn screening. , 2006, American journal of human genetics.

[31]  A. Mehta,et al.  Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey , 2004, European journal of clinical investigation.

[32]  M. Bullinger,et al.  Assessing health-related quality of life in chronically ill children with the German KINDL: first psychometric and content analytical results , 1998, Quality of Life Research.

[33]  U. Ramaswami,et al.  Enzyme replacement therapy with agalsidase alfa in children with Fabry disease , 2007, Acta paediatrica.

[34]  R. Schiffmann,et al.  Enhanced Endothelium-Dependent Vasodilation in Fabry Disease , 2001, Stroke.

[35]  S. Feriozzi,et al.  The effectiveness of long-term agalsidase alfa therapy in the treatment of Fabry nephropathy. , 2012, Clinical journal of the American Society of Nephrology : CJASN.

[36]  R. Schiffmann,et al.  Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease , 2000 .

[37]  P. Elliott,et al.  Impact of measures to enhance the value of observational surveys in rare diseases: the Fabry Outcome Survey (FOS). , 2011, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

[38]  R. Schiffmann,et al.  Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data , 2009, The Lancet.

[39]  R. Schiffmann,et al.  Enzyme replacement reverses abnormal cerebrovascular responses in Fabry disease , 2002, BMC neurology.

[40]  M. Beck,et al.  Effectiveness of agalsidase alfa enzyme replacement in Fabry disease: cardiac outcomes after 10 years’ treatment , 2015, Orphanet Journal of Rare Diseases.

[41]  S. Feriozzi,et al.  Kidney transplantation in patients with Fabry disease , 2009, Transplant international : official journal of the European Society for Organ Transplantation.

[42]  D. Hughes,et al.  Natural history of Fabry disease in females in the Fabry Outcome Survey , 2005, Journal of Medical Genetics.

[43]  P. Elliott,et al.  Natural course of Fabry disease: changing pattern of causes of death in FOS – Fabry Outcome Survey , 2009, Journal of Medical Genetics.

[44]  P. Elliott,et al.  Effects of enzyme replacement therapy on the cardiomyopathy of Anderson–Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa , 2007, Heart.

[45]  U. Ramaswami,et al.  Safety of agalsidase alfa in patients with Fabry disease under 7 years , 2011, Acta paediatrica.

[46]  A. Mehta,et al.  Hearing loss in Fabry disease: data from the Fabry Outcome Survey , 2006, European journal of clinical investigation.

[47]  T. Maisonobe,et al.  Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey , 2006, International journal of clinical practice.

[48]  Y. Chien,et al.  Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later‐onset GLA mutation c.936+919G>A (IVS4+919G>A) , 2009, Human mutation.

[49]  D. Stull,et al.  Measuring patient experiences in Fabry disease: validation of the Fabry-specific Pediatric Health and Pain Questionnaire (FPHPQ) , 2012, Health and Quality of Life Outcomes.

[50]  A. Mehta,et al.  Effects of enzyme replacement therapy with agalsidase alfa on glomerular filtration rate in patients with Fabry disease: preliminary data , 2003, Acta paediatrica (Oslo, Norway : 1992). Supplement.

[51]  S. Feriozzi,et al.  Enzyme replacement therapy and renal function in 201 patients with Fabry disease. , 2006, Clinical nephrology.

[52]  Shing‐Jong Lin,et al.  High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese Population , 2009, Circulation. Cardiovascular genetics.

[53]  N. Karabul,et al.  Ocular Signs Correlate Well with Disease Severity and Genotype in Fabry Disease , 2015, PLoS ONE.

[54]  R. Jaussaud,et al.  Fabry disease and the skin: data from FOS, the Fabry outcome survey , 2007, The British journal of dermatology.

[55]  A. Mehta,et al.  Agalsidase alpha and hearing in Fabry disease: data from the Fabry Outcome Survey , 2006, European journal of clinical investigation.

[56]  F. Bemelman,et al.  The Dutch Fabry cohort: Diversity of clinical manifestations and Gb3 levels , 2007, Journal of Inherited Metabolic Disease.

[57]  C. Eng,et al.  Fabry disease: twenty-three mutations including sense and antisense CpG alterations and identification of a deletional hot-spot in the alpha-galactosidase A gene. , 1994, Human molecular genetics.

[58]  C. Hollak,et al.  Limitations of drug registries to evaluate orphan medicinal products for the treatment of lysosomal storage disorders , 2011, Orphanet journal of rare diseases.

[59]  P. Bauer,et al.  Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study , 2005, The Lancet.

[60]  U. Ramaswami,et al.  Age adjusting severity scores for Anderson-Fabry disease. , 2010, Molecular genetics and metabolism.

[61]  C. Cleeland,et al.  Pain assessment: global use of the Brief Pain Inventory. , 1994, Annals of the Academy of Medicine, Singapore.

[62]  R. Brady,et al.  Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency. , 1967, The New England journal of medicine.

[63]  K. Ihara,et al.  Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot study , 2013, Journal of Human Genetics.

[64]  A. Mehta,et al.  Ocular manifestations of Fabry’s disease: data from the Fabry Outcome Survey , 2006, British Journal of Ophthalmology.

[65]  Carlene Campbell,et al.  Lysosomal storage disorder screening implementation: findings from the first six months of full population pilot testing in Missouri. , 2015, The Journal of pediatrics.

[66]  M. Sabbatini,et al.  Enzyme replacement therapy in patients with Fabry disease: state of the art and review of the literature. , 2012, Molecular genetics and metabolism.

[67]  A. Mehta,et al.  Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis , 2015, Molecular genetics and metabolism reports.

[68]  Wen-Chung Yu,et al.  Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A) , 2014, Orphanet Journal of Rare Diseases.

[69]  U. Ramaswami,et al.  Ear symptoms in children with Fabry disease: data from the Fabry Outcome Survey , 2009, Journal of Inherited Metabolic Disease.

[70]  A. Mehta,et al.  Effects of enzyme replacement therapy on pain and health related quality of life in patients with Fabry disease: data from FOS (Fabry Outcome Survey) , 2005, Journal of Medical Genetics.

[71]  K. Macdermot,et al.  Neuropathic pain in Anderson-Fabry disease: pathology and therapeutic options. , 2001, European journal of pharmacology.

[72]  W. van Biesen,et al.  Questioning the Pathogenic Role of the GLA p.Ala143Thr "Mutation" in Fabry Disease: Implications for Screening Studies and ERT. , 2012, JIMD reports.

[73]  A. Mehta,et al.  Gastrointestinal symptoms in 342 patients with Fabry disease: prevalence and response to enzyme replacement therapy. , 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

[74]  K. Macdermot,et al.  Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males , 2001, Journal of medical genetics.

[75]  P. Meikle,et al.  Prevalence of lysosomal storage disorders. , 1999, JAMA.

[76]  F. Tsai,et al.  Detecting multiple lysosomal storage diseases by tandem mass spectrometry--a national newborn screening program in Taiwan. , 2014, Clinica chimica acta; international journal of clinical chemistry.

[77]  P. Elliott,et al.  Fabry International Prognostic Index: a predictive severity score for Anderson-Fabry disease , 2012, Journal of Medical Genetics.

[78]  G. Houge,et al.  Fabry disease: overall effects of agalsidase alfa treatment , 2004, European journal of clinical investigation.