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Published on: October 18, 2011
Cognitive Functioning After Hematopoietic Cell Transplantation for Hematologic Malignancy: Results From a Prospective
Noha Sharafeldin1, Alysia Bosworth1, Sunita K Patel1
1Noha Sharafeldin, Liton Francisco, and Smita Bhatia, University of Alabama at Birmingham, Birmingham, AL; and Alysia Bosworth, Sunita K. Patel, Yanjun Chen, Emily Morse, Molly Mather, Canlan Sun, Stephen J. Forman, and F. Lennie Wong, City of Hope, Duarte, CA.
Cognitive impairment is significant after myeloablative allogeneic hematopoietic stem cell transplantation (HCT), but not after autologous HCT. Reduced-intensity allogeneic HCT shows delayed cognitive decline, highlighting the need for targeted interventions in vulnerable patient groups.
Area of Science:
- Neuroscience
- Hematology
- Oncology
Background:
- Cognitive impairment is a known complication following myeloablative allogeneic hematopoietic cell transplantation (HCT).
- The long-term cognitive effects of reduced-intensity allogeneic HCT and autologous HCT are less understood.
- Assessing cognitive function across different HCT types is crucial for patient care and outcome prediction.
Purpose of the Study:
- To compare cognitive functioning in patients undergoing myeloablative allogeneic, reduced-intensity allogeneic, and autologous HCT with healthy controls.
- To identify trends and risk factors associated with cognitive impairment after various HCT modalities.
- To evaluate the long-term impact of HCT on different cognitive domains.
Main Methods:
- A cohort of 477 HCT recipients (autologous, reduced-intensity allogeneic, myeloablative allogeneic) and 99 healthy controls underwent neuropsychological testing.
- Testing was conducted pre-HCT and at 6 months, 1, 2, and 3 years post-HCT.
- Statistical analysis using piecewise generalized estimating equation models compared cognitive scores and identified associated variables.
Main Results:
- Myeloablative allogeneic HCT recipients showed significant post-HCT cognitive decline in executive function, processing speed, and fine motor dexterity compared to controls.
- Autologous and reduced-intensity allogeneic HCT recipients had comparable cognitive scores to controls initially, but reduced-intensity recipients showed delayed decline in executive function and memory by 3 years.
- Older age, male sex, and lower socioeconomic/educational factors were associated with increased post-HCT cognitive impairment.
Conclusions:
- Myeloablative allogeneic HCT is associated with significant cognitive impairment, while autologous HCT generally spares cognitive function.
- Reduced-intensity allogeneic HCT recipients may experience delayed cognitive decline, suggesting a need for long-term monitoring.
- Identifying at-risk populations is essential for developing targeted interventions to mitigate cognitive deficits post-HCT.
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