Arterial stiffness and microvascular changes in adult Egyptian patients with beta-thalassemia and sickle cell anemia: a case-control study

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Authors: Rasha Rawi, Ibrahim Zaki Foad, Hala Aly Gamal El Din, Mary wadie fawzy, Hany William Z. Hanna, Mohamed Mahmoud Said, Maha Farouk Youssef Yacoub
Cited by: 1
References: 21

Abstract

Abstract Background Endothelial dysfunction is a key contributor to cardiovascular complications in patients with thalassemia and sickle cell disease (SCD), this dysfunction is linked to early atherosclerosis development. This study aimed to assess macrovascular and microvascular changes using non-invasive techniques and correlate them with clinical and laboratory parameters. Methods This case-control study included 94 adult participants (32 SCD, 32 thalassemia, and 32 healthy controls) between July 2023 to December 2024. We assessed endothelial function using flow-mediated dilatation (FMD), carotid-femoral pulse wave velocity (CF-PWV), and nailfold capillaroscopy (NFC), alongside laboratory investigations. Results FMD was significantly reduced in patient groups compared to controls ( p = 0.015), while CF-PWV showed no significant difference ( p = 0.593). NFC revealed significantly lower capillary density in patients ( p < 0.001). Hydroxyurea use was associated with better capillary density ( p = 0.043). Conclusion Patients with SCD and thalassemia exhibit early endothelial dysfunction, particularly at the microvascular level. NFC and FMD may serve as useful non-invasive tools for early detection, and hydroxyurea may have a protective vascular role.

Fields of Study & Subjects

Hemoglobinopathies and Related Disorders Blood properties and coagulation Iron Metabolism and Disorders

Publication details

Journal / source
The Egyptian Journal of Internal Medicine
Publisher
Springer Science and Business Media LLC
Volume
38
Issue
1
Publication date
28 May 2026
Language
EN