Iron Overload
Conditions
Keywords
iron overload, Thalassemia, Anemia, Sickle Cell, Magnetic Resonance Imaging
Brief summary
Sickle cell anemia and Sickle cell β thalassemia patients require multiple transfusions in order to avoid chronic anemia sequel. This regimen entails intrinsic deleterious effects, the majority of which are related to iron deposition in the reticuloendothelial system. Thus, iron is deposited in hepatic, myocardial and endocrine glands tissues. Tools available for iron load evaluation include serum ferrtin levels, liver biopsy and echocardiography, all are non specific. The purpose of this work is to compare iron overload in the liver, heart and pancreas in Sickle cell anemia and Sickle cell β thalassemia patients using T2\* MRI sequences.
Detailed description
Sickle cell anemia and Sickle cell β thalassemia patients recieving multiple transfusions are exposed to the effects of iron deposition in the reticuloendothelial system, including cardiac muscle, liver and pancreas. Tools available for iron load evaluation include serum ferrtin levels, liver biopsy and echocardiography, all are non specific. The purpose of this work is to compare iron overload in the liver, heart and pancreas in Sickle cell anemia and Sickle cell β thalassemia patients using T2\* MRI sequences. Patients and Methods: 27 Sickle cell anemia and 28 Sickle cell β thalassemia will undergo transthoracic echocardiography, cardiac MRI using T2\* sequences and clinical and laboratory evaluation for iron overload including ferritin levels and oral glucose tolerance test .
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* clinical diagnosis of Sickle cell anemia or Sickle cell β thalassemia having received multiple blood transfusions.
Exclusion criteria
* contraindication to MRI
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| outcome measure: iron overload on T2* MRI in the heart , liver and pancreas. | 1 year |
Countries
Israel