Early initiation of disease-modifying therapy can impede or prevent diffuse myocardial fibrosis in sickle cell anemia
Omar Niss, Jon Detterich, John C. Wood, Thomas D. Coates, Punam Malik, Michael D. Taylor, Charles T. Quinn
Abstract
Cardiovascular disease is a major cause of mortality in patients with sickle cell disease (SCD). Niss et al previously reported that cardiac magnetic resonance in 25 patients showed universal myocardial fibrosis, which they correlated with increased extracellular volume fraction (ECV). In the current study, they compared patients with SCD who were treated with hydroxyurea or transfusion at age <6 years to a group of patients with SCD without therapy. They documented that patients treated early had ECV levels comparable to normal controls, potentially preventing subsequent myocardial fibrosis.
Topics & Concepts
MedicineMyocardial fibrosisAnemiaSickle cell anemiaDiseaseFibrosisInternal medicineTransfusion therapyCardiologyGastroenterologyBlood transfusionHemoglobinopathies and Related DisordersCardiovascular Function and Risk FactorsIron Metabolism and Disorders