Related Experiment Video
Updated: May 15, 2026

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
Developmental function in toddlers with sickle cell anemia
F Daniel Armstrong1, T David Elkin, R Clark Brown
1Department of Pediatrics (D-820), PO Box 016820, Miami, FL 33101, USA. darmstrong@miami.edu
Insights
In infants with sickle cell disease, neurodevelopment is generally average, but behavioral and adaptive functions decline with age. Further research is needed to understand these developmental changes.
Area of Science:
- Pediatric Neurology
- Hematology
- Developmental Psychology
Background:
- Neurocognitive impairment is recognized in children and adults with sickle cell anemia.
- Limited data exists on neurodevelopmental outcomes in very young children with sickle cell disease.
Purpose of the Study:
- To assess the neurodevelopmental status of infants in the Pediatric Hydroxyurea Phase III Clinical Trial (Baby Hug).
- To investigate the relationships between neurodevelopment, age, cerebral blood flow velocity, and hemoglobin concentration in infants with sickle cell disease.
Main Methods:
- 193 infants (hemoglobin SS or S-β(0) thalassemia) aged 7–18 months underwent standardized neurodevelopmental assessments.
- Evaluated associations between neurodevelopmental scores and age, income, education, hemoglobin levels, and transcranial Doppler velocity.
Main Results:
- Mean neurodevelopmental functioning was within the average range.
- No infants had impaired mental development scores (<70); however, 22 had clinically significant scores (11 psychomotor, 11 behavioral).
- Poorer performance correlated with older age at baseline; behavior ratings decreased by 2.82 percentile points per month of age. Parent-reported functional abilities and hemoglobin levels showed a negative association with higher transcranial Doppler velocities.
Conclusions:
- Overall neurodevelopmental functioning in infants with sickle cell disease is within the normal range.
- Behavioral and adaptive functioning showed a decline with increasing age, even in this young cohort.
- Further research is required to elucidate the mechanisms underlying the association between poorer developmental function and older age in this population.
Background:
Neurocognitive impairment occurs in children and adults with sickle cell anemia, but little is known about neurodevelopment in very young children. We examined the neurodevelopmental status of infants participating in the Pediatric Hydroxyurea Phase III Clinical Trial (Baby Hug) to determine relationships with age, cerebral blood flow velocity, and hemoglobin concentration.
Methods:
Standardized measures of infant neurodevelopment were administered to 193 infants with hemoglobin SS or hemoglobin S-β(0) thalassemia between 7 and 18 months of age at the time of their baseline evaluation. Associations between neurodevelopmental scores and age, family income, parent education, hemoglobin concentration, and transcranial Doppler velocity were examined.
Results:
Mean functioning on the baseline neurodevelopment scales was in the average range. There were no mental development scores <70 (impaired); 22 children had scores in the clinically significant range, 11 with impaired psychomotor scores and 11 with problematic behavior rating scores. Significantly poorer performance was observed with older age at baseline. Behavior rating scores were an average of 2.82 percentile points lower per month of age, with similar patterns observed with parent report using adaptive behavior scales. Parent-reported functional abilities and hemoglobin were negatively associated with higher transcranial Doppler velocities.
Conclusions:
Whereas overall functioning was in the normal range, behavioral and adaptive function was poorer with older age, even in this very young group of children. Explanatory mechanisms for this association between poorer developmental function and older age need to be identified.
Related Concept Videos
Multiple Allele Traits
Overview of Hematopoiesis
Developmental Phases of Hematopoiesis
Initially, HSCs are formed in the embryonic yolk sac, a critical site for early blood cell production. These stem cells subsequently migrate to other...
Socioemotional Development during Infancy
Primary Temperament Types
Stella Chess...
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...
Immunodeficiency Diseases
There are three main causes of immunodeficiency disorders...
Role of Hematopoietic Growth Factors
Thrombopoietin (TPO), mainly released by the liver,...
