Athanasios Aessopos (a), Dimitrios Farmakis (a), Maria Tsironi (a), Evanthia Diamanti-Kandarakis (a), Marina Matzourani (a), Christina Fragodimiri (b), Antonia Hatziliami (b) and Markisia Karagiorga (b)
a) First Department of Internal Medicine, University of Athens Medical School, Laiko Hospital, 17 Aghiou Thoma St., Athens 115 27, Greece
b) Thalassemia Unit, Aghia Sophia Children's Hospital, Athens, Greece
Background. Homozygous sickle-cell anemia and β-thalassemia are characterized by impaired endothelial function, while data on arterial stiffness have hitherto been conflicting. We sought to investigate aortic elastic properties and endothelial function in sickle-thalassemia, which combines molecular and clinical features of the above conditions.
Methods and results. Forty-seven sickle-thalassemia patients, younger than 45 years, with preserved left ventricular (LV) function and no history of smoking, systemic or pulmonary hypertension, diabetes mellitus, dyslipidemia or thyroid disease, along with 40 healthy controls were studied. Aortic strain, distensibility and stiffness index were calculated by echocardiographically-obtained aortic root diameters. Brachial artery endothelial function was assessed by ultrasonographic evaluation of flow-mediated dilatation (FMD) and nitrate-mediated dilatation (NMD). Left ventricle was assessed by echocardiography. Patients had an impaired FMD (4.2 ± 2.9% versus 9.2 ± 3.8% in controls, p <> 0.05). Aortic strain and distensibility were lower and aortic stiffness index was higher in patients compared to controls (8.1 ± 4.6 versus 5.8 ± 2.9, p <>
Conclusion. Sickle-thalassemia is characterized by a complex vasculopathy, consisting of endothelial dysfunction and increased arterial stiffness, with a global effect on cardiovascular function.
Keywords: Thalassemia; Sickle-cell disease; Endothelial function; Arterial stiffness
Atherosclerosis Volume 191, Issue 2 , April 2007, Pages 427-432
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