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Blood. 2019 May 30;133(22):2436-2444. doi: 10.1182/blood-2018-09-876318. Epub 2019 Mar 11.

Hydroxyurea reduces cerebral metabolic stress in patients with sickle cell anemia.

Author information

1
Division of Pediatric Hematology/Oncology.
2
Division of Pediatric Neurology, and.
3
Division of Pediatric Critical Care Medicine, Washington University School of Medicine, St. Louis, MO.
4
Department of Radiology, Medical College of Wisconsin, Milwaukee, WI; and.
5
Department of Biomedical Engineering.
6
Department of Neurology.
7
Division of Hematology, and.
8
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.

Abstract

Chronic transfusion therapy (CTT) prevents stroke in selected patients with sickle cell anemia (SCA). We have shown that CTT mitigates signatures of cerebral metabolic stress, reflected by elevated oxygen extraction fraction (OEF), which likely drives stroke risk reduction. The region of highest OEF falls within the border zone, where cerebral blood flow (CBF) nadirs; OEF in this region was reduced after CTT. The neuroprotective efficacy of hydroxyurea (HU) remains unclear. To test our hypothesis that patients receiving HU therapy have lower cerebral metabolic stress compared with patients not receiving disease-modifying therapy, we prospectively obtained brain magnetic resonance imaging scans with voxel-wise measurements of CBF and OEF in 84 participants with SCA who were grouped by therapy: no disease-modifying therapy, HU, or CTT. There was no difference in whole-brain CBF among the 3 cohorts (P = .148). However, whole-brain OEF was significantly different (P < .001): participants without disease-modifying therapy had the highest OEF (median 42.9% [interquartile range (IQR) 39.1%-49.1%]), followed by HU treatment (median 40.7% [IQR 34.9%-43.6%]), whereas CTT treatment had the lowest values (median 35.3% [IQR 32.2%-38.9%]). Moreover, the percentage of white matter at highest risk for ischemia, defined by OEF greater than 40% and 42.5%, was lower in the HU cohort compared with the untreated cohort (P = .025 and P = .034 respectively), but higher compared with the CTT cohort (P = .018 and P = .029 respectively). We conclude that HU may offer neuroprotection by mitigating cerebral metabolic stress in patients with SCA, but not to the same degree as CTT.

PMID:
30858231
PMCID:
PMC6543515
[Available on 2020-05-30]
DOI:
10.1182/blood-2018-09-876318

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