Regional oxygen extraction predicts border zone vulnerability to stroke in sickle cell disease

• Published in: Neurology Vol. 90; no. 13; pp. e1134 - e1142
• Main Authors: Fields, Melanie E, Guilliams, Kristin P, Ragan, Dustin K, Binkley, Michael M, Eldeniz, Cihat, Chen, Yasheng, Hulbert, Monica L, McKinstry, Robert C, Shimony, Joshua S, Vo, Katie D, Doctor, Allan, An, Hongyu, Ford, Andria L, Lee, Jin-Moo
• Format: Journal Article
• Language: English
• Published: United States American Academy of Neurology 27-03-2018; Lippincott Williams & Wilkins
• Subjects: Adolescent; Anemia, Sickle Cell - diagnostic imaging; Anemia, Sickle Cell - metabolism; Anemia, Sickle Cell - therapy; Brain - diagnostic imaging; Brain - metabolism; Cerebrovascular Circulation; Child; Child, Preschool; Cohort Studies; Female; Humans; Image Interpretation, Computer-Assisted - methods; Magnetic Resonance Imaging - methods; Male; Oxygen - metabolism; Oxygen Consumption; Stroke - diagnostic imaging; Stroke - metabolism; Young Adult
• ISSN: 0028-3878; 1526-632X
• DOI: 10.1212/WNL.0000000000005194

OBJECTIVETo determine mechanisms underlying regional vulnerability to infarction in sickle cell disease (SCD) by measuring voxel-wise cerebral blood flow (CBF), oxygen extraction fraction (OEF), and cerebral metabolic rate of oxygen utilization (CMRO2) in children with SCD.
METHODSParticipants underwent brain MRIs to measure voxel-based CBF, OEF, and CMRO2. An infarct heat map was created from an independent pediatric SCD cohort with silent infarcts and compared to prospectively obtained OEF maps.
RESULTSFifty-six participants, 36 children with SCD and 20 controls, completed the study evaluation. Whole-brain CBF (99.2 vs 66.3 mL/100 g/min, p < 0.001), OEF (42.7% vs 28.8%, p < 0.001), and CMRO2 (3.7 vs 2.5 mL/100 g/min, p < 0.001) were higher in the SCD cohort compared to controls. A region of peak OEF was identified in the deep white matter in the SCD cohort, delineated by a ratio map of average SCD to control OEF voxels. CMRO2 in this region, which encompassed the CBF nadir, was low relative to all white matter (p < 0.001). Furthermore, this peak OEF region colocalized with regions of greatest infarct density derived from an independent SCD cohort.
CONCLUSIONSElevated OEF in the deep white matter identifies a signature of metabolically stressed brain tissue at increased stroke risk in pediatric patients with SCD. We propose that border zone physiology, exacerbated by chronic anemic hypoxia, explains the high risk in this region.