Early indicators of disease progression in Fabry disease that may indicate the need for disease-specific treatment initiation: findings from the opinion-based PREDICT-FD modified Delphi consensus initiative
James C Moon,
Albina Nowak,
Derralynn A Hughes,
Mark Thomas,
Raphael Schiffmann,
Ales Linhart,
David G Warnock,
Sandro Feriozzi,
Patricio Aguiar,
Patrick B Deegan,
Fatih Ezgu,
Andrea Frustaci,
Olivier Lidove,
Jean-Claude Lubanda,
Kathleen Nicholls,
Dau-Ming Niu,
Uma Ramaswami,
Ricardo Reisin,
Paula Rozenfeld,
Einar Svarstad,
Roser Torra,
Bojan Vujkovac,
Michael L West,
Jack Johnson,
Mark J Rolfe
Affiliations
James C Moon
3Cardiac MRI Unit, Barts Heart Centre, West Smithfield, London
Albina Nowak
2 Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich, Zurich, Switzerland
Derralynn A Hughes
Department of Haematology, University College London, London, UK
Mark Thomas
2Oxford Vacmedix, Oxford, Oxfordshire, UK
Raphael Schiffmann
Institute of Metabolic Disease, Baylor Research Institute, Dallas, Texas, USA
Ales Linhart
Department of Internal Medicine, School of Medicine, Charles University and General University Hospital, Prague, Czech Republic
David G Warnock
Division of Nephrology, University of Alabama at Birmingham, Birmingham, Alabama, USA
Sandro Feriozzi
Division of Nephrology, Belcolle Hospital, Viterbo, Italy
Patricio Aguiar
Inborn Errors of Metabolism Reference Center, North Lisbon Hospital Center, Lisbon, Portugal
Patrick B Deegan
Lysosmal Disorders Unit, Department of Medicine, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK
Fatih Ezgu
Department and Laboratory of Paediatric Metabolic Disorders, Gazi University, Ankara, Turkey
Andrea Frustaci
Department of Cardiovascular, Respiratory, Nephrologic, Geriatric and Anesthesiologic Sciences, University of Rome La Sapienza, Rome, Italy
Olivier Lidove
2Croix Saint Simon Hospital, Paris, France
Jean-Claude Lubanda
Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic
Kathleen Nicholls
Department of Medicine, The University of Melbourne - Parkville Campus, Melbourne, Victoria, Australia
Dau-Ming Niu
Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan
Uma Ramaswami
Lysosomal Storage Disorders Unit, Royal Free London NHS Foundation Trust, London, UK
Ricardo Reisin
Department of Neurology, British Hospital of Buenos Aires, Buenos Aires, Argentina
Paula Rozenfeld
Instituto de Estudios Inmunológicos y Fisiopatológicos, UNLP - CONICET, La Plata, Argentina
Einar Svarstad
Department of Clinical Medicine, University of Bergen, Bergen, Norway
Roser Torra
Inherited Renal Disorders, Nephrology Department, Fundació Puigvert, IIB Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain
Bojan Vujkovac
Department of Internal Medicine, General Hospital Slovenj Gradec, Slovenj Gradec, Slovenia
Michael L West
Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
Jack Johnson
Fabry Support & Information Group, Concordia, Missouri, USA
Objectives The PRoposing Early Disease Indicators for Clinical Tracking in Fabry Disease (PREDICT-FD) initiative aimed to reach consensus among a panel of global experts on early indicators of disease progression that may justify FD-specific treatment initiation.Design and setting Anonymous feedback from panellists via online questionnaires was analysed using a modified Delphi consensus technique. Questionnaires and data were managed by an independent administrator directed by two non-voting cochairs. First, possible early indicators of renal, cardiac and central/peripheral nervous system (CNS/PNS) damage, and other disease and patient-reported indicators assessable in routine clinical practice were compiled by the cochairs and administrator from panellists’ free-text responses. Second, the panel scored indicators for importance (5-point scale: 1=not important; 5=extremely important); indicators scoring ≥3 among >75% of panellists were then rated for agreement (5-point scale: 1=strongly disagree; 5=strongly agree). Indicators awarded an agreement score ≥4 by >67% of panellists achieved consensus. Finally, any panel-proposed refinements to consensus indicator definitions were adopted if >75% of panellists agreed.Results A panel of 21 expert clinicians from 15 countries provided information from which 83 possible current indicators of damage (kidney, 15; cardiac, 15; CNS/PNS, 13; other, 16; patient reported, 24) were compiled. Of 45 indicators meeting the importance criteria, consensus was reached for 29 and consolidated as 27 indicators (kidney, 6; cardiac, 10; CNS/PNS, 2; other, 6; patient reported, 3) including: (kidney) elevated albumin:creatinine ratio, histological damage, microalbuminuria; (cardiac) markers of early systolic/diastolic dysfunction, elevated serum cardiac troponin; (CNS/PNS) neuropathic pain, gastrointestinal symptoms suggestive of gastrointestinal neuropathy; (other) pain in extremities/neuropathy, angiokeratoma; (patient-reported) febrile crises, progression of symptoms/signs. Panellists revised and approved proposed chronologies of when the consensus indicators manifest. The panel response rate was >95% at all stages.Conclusions PREDICT-FD captured global opinion regarding current clinical indicators that could prompt FD-specific treatment initiation earlier than is currently practised.