DRAFT AGENDA |
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Monday, October 27, 2008 |
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| 7:15 a.m. – 8:00 a.m. | Registration and Continental Breakfast |
| Introductions and Overviews | |
| 8:00 a.m. – 8:15 a.m. | Welcome and Workshop Introduction |
| 8:15 a.m. – 9:15 a.m. | Overview: Iron Overload as a Global Health Burden |
| Mechanisms Underlying Iron Overload | |
| 9:15 a.m. – 9:45 a.m. | Diverse Mechanisms of Hepcidin Deficiency or Hepcidin Resistance in Hereditary Hemochromatosis Tomas Ganz, Geffen School of Medicine, UCLA, Los Angeles, CA |
| 9:45 a.m. – 10:15 a.m. | The Molecular Basis and Consequences of Hepcidin Mediated Ferroportin Downregulation Ivana DeDomenico, University of Utah Sch. of Medicine, Salt Lake City, UT |
| 10:15 a.m. – 10:30 a.m. | Break |
| 10:30 a.m. – 11:00 a.m. | Multiple Roles of Hemojuvelin in Iron Deficiency and Overload Clara Camaschella, Università Vita-Salute San Raffaele, Milano, Italy |
| 11:00 a.m. – 11:30 a.m. | Hereditary Hemochromatosis: An Eclectic Family of Dysfunctional Proteins Carolyn Enns, Oregon Health & Science University, Portland, OR |
| 11:30 a.m. – 12:00 p.m. | Regulatory Mechanisms in Hereditary Hemochromatosis Martina Muckenthaler, University of Heidelberg, Heidelberg, Germany |
| 12:00 p.m. – 12:30 p.m. | Enteric Regulation of Iron Absorption Richard Ajioka, University of Utah School of Medicine, Salt Lake City, UT |
| 12:30 p.m. – 2:00 p.m. | Lunch |
| 2:00 p.m. – 2:30 p.m. | Role of TMPRSS6, a Type II Transmembrane Serine Protease, in the Control of Systemic Iron Homeostasis in Humans Karin Finberg, Duke University Medical Center, Durham, NC |
| 2:30 p.m. – 3:00 p.m. | Pathological Iron Overload Due to Ineffective Erythropoiesis Jeff Miller, Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH), Bethesda, MD |
| 3:00 p.m. – 3:30 p.m. | Differing Patterns of Transfusional Iron Overload in Thalassemia and Sickle Cell Disease: Clinical Observations and Possible Mechanisms Elliott Vichinsky, Children’s Hospital Oakland Research Institute, Oakland, CA John Porter, Haematology Division, University College, London, UK |
| 3:30 p.m. – 3:45 p.m. | Break |
| 3:45 p.m. – 4:15 p.m. | Pathophysiology of Iron-Related Toxicty Kris Kowdley, Center for Liver Disease, Virginia Mason Medical Center, Seattle, WA |
| 4:15 p.m. – 4:45 p.m. | Hepcidin as a Novel Diagnostic Test: Analysis and Clinical Applicability Dorine Swinkels, Radboud University Medical Center, Nijmegen, Netherlands |
| 4:45 p.m. – 5:15 p.m. | Serum Hepcidin Immunoassay Elizabeta Nemeth, University of California – Los Angeles, Department of Medicine, Los Angeles, CA |
| Presentations from Poster Presenters | |
| 5:15 p.m. – 6:15 p.m. | Selected Concise Presentations from Abstracts |
| 6:15 p.m. – 7:00 p.m. | Poster Presentations (followed by dinner) |
Tuesday, October 28, 2008 |
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| 7:15 a.m. – 8:00 a.m. | Registration and Continental Breakfast |
| Measuremen of Iron Overload: Degree, Distribution, and Duration | |
| 8:00 a.m. – 8:30 a.m. | Imaging Organ Iron: Influence of Particle Size and Distribution |
| 8:30 a.m. – 9:00 a.m. | Myocardial Siderosis Assessment by T2* Dudley Pennell, Imperial College, Royal Brompton Hospital, London |
| 9:00 a.m. – 9:30 a.m. | Tissue Iron Measurement Using Quantitative R2 Relaxometry – Applications in Hereditary Haemochromatosis and Alzheimer’s Disease Michael House, School of Physics, University of West Australia, Crawley, Australia |
| 9:30 a.m. – 10:00 a.m. | Separate MRI Quantification of Dispersed (Ferritin-like) and Aggregated (Hemosiderin-like) Storage Iron Jens Jensen, Center for Biomedical Imaging, Department of Radiology, New York University, New York, NY |
| 10:00 a.m. – 10:30 a.m. | Break |
| 10:30 a.m. – 11:00 a.m. | Non-Invasive Assessment of Tissue Iron: The Meaning of the Measurements Gary Brittenham, Columbia University, Children's Hospital of New York, New York, NY |
| Management of Iron Overload: Current Methods and Novel Approaches | |
| 11:00 a.m. – 11:30 a.m. | Should the Availability of New Diagnostic Methods and New Chelation Regimes Change Our Treatment Goals for Transfusional Iron Overload? John Porter, Haematology, University College, London, UK |
| 11:30 a.m. – 12:00 p.m. | Tailoring Iron Chelation to the Needs of the Patients Renzo Galanello, University di Cagliari, Ospedale Regionale Microcitemie, Cagliari, Italy |
| 12:00 p.m. – 12:30 p.m. | The Role of Transfusion Therapy in the Management of Iron Overload Alan Cohen, Children's Hospital of Pennsylvania, University of Pennslyvania, Philadelphia, PA |
| 12:30 p.m. – 2:00 p.m. | Lunch |
| 2:00 p.m. – 2:30 p.m. | Disorders Associated with Iron Misdistribution: The Therapeutic Potential for Siderophores Z. Ioav Cabantchik, Life Sciences Institute, Hebrew University, Jerusalem, Israel |
| 2:30 p.m. – 3:00 p.m. | The Desferrithiocin Pharmacophore: A Structure Activity Study Ray Bergeron, University of Florida, Gainesville, FL |
| 3:00 p.m. – 3:30 p.m. | Going for the Iron: Targeting Chelators to Ferritin |
| Summary Commentary | |
| 3:30 p.m. – 4:00 p.m. | Nancy Andrews, Duke University Medical Center, Durham, NC Jerry Kaplan, University of Utah School of Medicine, Salt Lake City, UT |
| 4:00 p.m. | Workshop adjourns |








