Cerebral hemodynamic assessment and neuroimaging across the lifespan in sickle cell disease

Lori C Jordan1, Michael R DeBaun2

  • 11 Department of Pediatrics, Division of Pediatric Neurology, Vanderbilt University Medical Center, Nashville, TN, USA.

Insights

Sickle cell anemia (SCA) increases stroke risk. New MRI methods may help identify high-risk individuals for better stroke prevention and management in both children and adults.

Area of Science:

  • Neurology
  • Radiology
  • Hematology

Background:

  • Sickle cell anemia (SCA) patients face elevated stroke risks compared to peers.
  • Transcranial Doppler identifies high-risk children but not adults for initial strokes.
  • Current methods lack efficacy in identifying recurrent stroke or silent stroke risks in SCA patients.

Purpose of the Study:

  • To review stroke epidemiology, mechanisms, and impact in SCA.
  • To explore advanced neuroimaging strategies for stroke risk assessment in SCA.
  • To identify individuals at high risk for initial and recurrent strokes.

Main Methods:

  • Review of existing literature on stroke in SCA.
  • Discussion of transcranial Doppler ultrasound limitations.
  • Exploration of contrast-free MRI techniques for cerebral hemodynamics assessment.

Main Results:

  • Stroke is a significant complication in both pediatric and adult SCA patients.
  • Existing methods for stroke risk stratification in SCA are limited, especially for adults and recurrent events.
  • Advanced MRI techniques offer promising alternatives for assessing cerebral hemodynamics without radiotracers.

Conclusions:

  • Improved neuroimaging is crucial for identifying SCA patients at high risk of initial and recurrent strokes.
  • Contrast-free MRI holds potential for feasible screening and longitudinal monitoring of cerebral hemodynamics in SCA.
  • Enhanced risk identification can guide more aggressive, tailored therapies to prevent stroke complications.

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