Related Experiment Video
Updated: Oct 26, 2025

Endothelialized Microfluidics for Studying Microvascular Interactions in Hematologic Diseases
Published on: June 22, 2012
Effects of hydroxyurea on brain function in children with sickle cell anemia
Winfred C Wang1, Ping Zou2, Scott N Hwang2
1Department of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Insights
Hydroxyurea treatment improved neurocognitive function and reduced brain blood flow velocity in children with sickle cell anemia (SCA). These findings suggest hydroxyurea can enhance brain health in SCA patients.
Area of Science:
- Neurology
- Pediatrics
- Hematology
Background:
- Sickle cell anemia (SCA) is a genetic blood disorder with significant neurological complications, including cognitive impairment.
- The long-term effects of hydroxyurea, a common SCA treatment, on brain function remain unclear.
Purpose of the Study:
- To prospectively evaluate the impact of one year of hydroxyurea treatment on brain function in children with SCA.
- To assess changes in neurocognitive performance, cerebral blood flow, and brain imaging markers.
Main Methods:
- A cohort of 19 children with SCA (HbSS/HbSβ0-thalassemia) underwent comprehensive neurocognitive testing, transcranial Doppler ultrasound (TCD), and brain MRI at baseline and after one year of hydroxyurea therapy.
- Evaluated parameters included Full-Scale IQ (FSIQ), silent cerebral infarcts (SCI), gray matter cerebral blood flow (GM-CBF), and BOLD signal response to visual stimulation.
Main Results:
- After one year, patients showed significant improvements in FSIQ and reading comprehension, alongside a marked decrease in TCD velocity.
- No significant changes were observed in GM-CBF, BOLD signal, or SCI frequency.
- Correlations were found between neurocognitive outcomes and levels of Hemoglobin F (HbF), hemoglobin, GM-CBF, and BOLD signal.
Conclusions:
- One year of hydroxyurea treatment demonstrates potential benefits for neurocognitive outcomes and cerebrovascular health in children with SCA.
- Further research is needed to elucidate the precise mechanisms underlying these improvements, particularly the relationships between HbF, hemoglobin, cerebral blood flow, and cognitive function.
Introduction:
Sickle cell anemia (SCA) results in numerous adverse effects on the brain, including neurocognitive dysfunction. Hydroxyurea has been utilized extensively for management of SCA, but its effects on brain function have not been established.
Methods:
We examined prospectively the effects of 1 year of treatment with hydroxyurea on brain function in children with SCA (HbSS/HbSβ0 -thalassemia) by baseline and exit evaluations, including comprehensive neurocognitive testing, transcranial Doppler ultrasound (TCD), and brain MRI (silent cerebral infarcts [SCI], gray matter cerebral blood flow [GM-CBF], and blood oxygen level-dependent [BOLD] signal from visual stimulation).
Results:
Nineteen patients with SCA, mean age 12.4 years (range 7.2-17.8), were evaluated. At baseline, subjects had these mean values: full-scale IQ (FSIQ) 82.8, TCD velocity 133 cm/s, GM-CBF 64.4 ml/100 g/min, BOLD signal 2.34% increase, and frequency of SCI 47%. After 1 year of hydroxyurea, there were increases in FSIQ (+2, p = .059) and reading passage comprehension (+4, p = .033), a significant decrease in TCD velocity (-11 cm/s, p = .007), and no significant changes in GM-CBF, BOLD, or SCI frequency. Hemoglobin F (HbF) was associated with passage comprehension, hemoglobin with lower TCD velocity, and lower GM-CBF with greater working memory. Higher BOLD signal was associated with higher processing speed and lower TCD velocity with higher math fluency.
Discussion:
Improvements in neurocognition and decreased TCD velocity following 1 year of treatment support hydroxyurea use for improving neurocognitive outcomes in SCA. Understanding the mechanisms of benefit, as indicated by relationships of neurocognitive function with HbF, hemoglobin, and CBF, requires further evaluation.
More Related Videos
05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
07:24A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Drug Excretion
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Lysosomal Hydrolases
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Disorders of Erythrocytes
Erythrocyte disorders can be broadly categorized into two main types: anemic and polycythemic conditions.
A low oxygen-carrying capacity of the blood due to the loss, lower production, or destruction of erythrocytes is termed anemia. Hemorrhagic anemia, for example, occurs when bleeding from an external wound or internal ulcer reduces erythrocyte counts.
On the other...