Brain-derived Neurotrophic Factor Levels in Pediatric Sickle Cell Disease
Overview
Oncology
Pediatrics
Affiliations
Background: Children with sickle cell disease (SCD) have an increased risk of neurological complications, particularly stroke and silent cerebral infarction (SCI). Brain-derived neurotrophic factor (BDNF) is a nerve growth factor associated with neuronal survival, synaptic plasticity, elevated transcranial Doppler (TCD) velocities and increased risk of stroke in patients with SCD. The objective of this study was to analyze plasma BDNF protein levels in children with SCD participating in the Silent Cerebral Infarct Transfusion Multi-Center Clinical Trial (SIT Trial), comparing plasma samples of children with SCD and SCI to plasma samples from children with SCD without SCI, as well as healthy pediatric control participants.
Procedure: Entry, exit, and longitudinal blood samples were collected from 190 SIT Trial participants with SCD and healthy pediatric controls over time. BDNF levels were measured by enzyme-linked immunosorbent assay. Sample collection was not optimized for measurements of BDNF, but factors affecting BDNF levels were accounted for in analyses.
Results: BDNF levels were significantly higher in children with SCD in comparison to healthy pediatric control subjects. BDNF levels significantly increased over time in SCD participants. BDNF levels did not show any significant associations with the presence or absence of SCI or new/progressive SCI/stroke or TCD velocities.
Conclusions: Plasma BDNF levels are elevated and increase over time in children with SCD. Additional studies with more longitudinal samples are needed to address the reasons for those increased levels.
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Lekpor C, Botchway F, Driss A, Bashi A, Abrahams A, Kusi K Front Mol Biosci. 2025; 11:1481441.
PMID: 39749215 PMC: 11694143. DOI: 10.3389/fmolb.2024.1481441.
Brain-derived neurotrophic factor and neuroimaging in pediatric patients with sickle cell disease.
Mahmoud A, Abd El Naby S, Abdelgawad A, Rizq M, Abd El Hady N Pediatr Res. 2023; 93(7):1922-1926.
PMID: 36774398 PMC: 10313519. DOI: 10.1038/s41390-023-02513-5.
Chambliss C, Richardson T, Onyekaba J, Cespedes J, Nti A, Oxendine Harp K Endocr Metab Sci. 2022; 3.
PMID: 35935682 PMC: 9351492. DOI: 10.1016/j.endmts.2021.100088.
Lance E, Faulcon L, Fu Z, Yang J, Whyte-Stewart D, Strouse J Proteomics Clin Appl. 2021; 15(5):e2100003.
PMID: 33915030 PMC: 8666096. DOI: 10.1002/prca.202100003.