Frontiers in Neurology (May 2024)

Neurocognitive outcome in children with sickle cell disease after myeloimmunoablative conditioning and haploidentical hematopoietic stem cell transplantation: a non-randomized clinical trial

  • Suzanne Braniecki,
  • Elliott Vichinsky,
  • Mark C. Walters,
  • Shalini Shenoy,
  • Qiuhu Shi,
  • Theodore B. Moore,
  • Julie-An Talano,
  • Susan K. Parsons,
  • Allyson Flower,
  • Anne Panarella,
  • Sandra Fabricatore,
  • Erin Morris,
  • Harshini Mahanti,
  • Jordan Milner,
  • Robert C. McKinstry,
  • Robert C. McKinstry,
  • Christine N. Duncan,
  • Carmella van de Ven,
  • Mitchell S. Cairo,
  • Mitchell S. Cairo,
  • Mitchell S. Cairo,
  • Mitchell S. Cairo,
  • Mitchell S. Cairo

DOI
https://doi.org/10.3389/fneur.2024.1263373
Journal volume & issue
Vol. 15

Abstract

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BackgroundDue to the risk of cerebral vascular injury, children and adolescents with high-risk sickle cell disease (SCD) experience neurocognitive decline over time. Haploidentical stem cell transplantation (HISCT) from human leukocyte antigen-matched sibling donors may slow or stop progression of neurocognitive changes.ObjectivesThe study is to determine if HISCT can ameliorate SCD-associated neurocognitive changes and prevent neurocognitive progression, determine which specific areas of neurocognitive functioning are particularly vulnerable to SCD, and determine if there are age-related differences in neurocognitive functioning over time.MethodsWe performed neurocognitive and neuroimaging in SCD recipients following HISCT. Children and adolescents with high-risk SCD who received parental HISCT utilizing CD34+ enrichment and mononuclear cell (T-cell) addback following myeloimmunoablative conditioning received cognitive evaluations and neuroimaging at three time points: pre-transplant, 1 and 2 years post-transplant.ResultsNineteen participants (13.1 ± 1.2 years [3.3–20.0]) received HISCT. At 2 years post-transplant, neuroimaging and cognitive function were stable. Regarding age-related differences pre-transplantation, older children (≥13 years) had already experienced significant decreases in language functioning (p < 0.023), verbal intelligence quotient (p < 0.05), non-verbal intelligence quotient (p < 0.006), and processing speed (p < 0.05), but normalized post-HISCT in all categories.ConclusionThus, HISCT has the potential to ameliorate SCD-associated neurocognitive changes and prevent neurocognitive progression. Further studies are required to determine if neurocognitive performance remains stable beyond 2 years post-HISCT.Clinical trial registration: The study was conducted under an investigator IND (14359) (MSC) and registered at clinicaltrials.gov (NCT01461837).

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