Blood transfusions are often administered for secondary stroke prevention in adults with sickle cell anemia (SCA). We utilized noninvasive MRI methods to evaluate how oxygen extraction fraction (OEF) and cerebral blood flow (CBF) adjust after transfusion in adults with SCA. OEF reduced on average, while CBF did not change significantly. The OEF reduction paralleled increases in hematocrit but was unrelated to the reduction in hemoglobin-S. This implies that most patients receiving transfusions operate near autoregulatory reserve capacity even after transfusion, and improving oxygen delivery by increasing hematocrit can be visualized noninvasively with OEF-MRI.
Study participants. Adults with SCA genotype hemoglobin SS or S-β0 thalassemia (n=17; age=25.8±6.7 years) receiving simple or modified-exchange transfusions and healthy controls without sickle trait (n=7; age=26.1±6.2 years) were scanned at 3.0T (Philips) at two time points. For SCA participants, this included one scan late in their transfusion cycle when blood hematocrit was near nadir and a second scan within 7 days of transfusion. All volunteers provided informed written consent.
Experiment. T1-weighted imaging (MPRAGE; TR/TE=8.2/3.7ms; spatial resolution=1.0x1.0x1.0mm3), TRUST-MRI (repeats per session=2; TR/TE=1978/3.6 ms; spatial resolution=3.4x3.4x5 mm3; tCPMG=10ms; eTE=0, 40, 80, and 160ms)6, 7, and phase contrast MRA (spatial resolution=0.5x0.5 mm2; TR/TE = 20/7 ms; with velocity-encoding gradient=40 cm/s) were acquired for tissue volume, OEF, and CBF determination, respectively. Arterial oxygen saturation (Ya) was measured using peripheral pulse oximetry, and blood hematocrit and HbS% were measured through venipuncture on the day of imaging. Phase contrast data were acquired for each of the four primary vessels supplying the brain: left internal carotid artery (ICA), right ICA, left vertebral, and right vertebral
Analysis. T1-weighted images were segmented to quantify total tissue volume. Venous oxygenation (Yv) values in the superior sagittal sinus were quantified from TRUST MRI data as previously described5. Yv was then used, along with Ya, to compute OEF as (Ya-Yv)/Ya. Whole-brain CBF values were quantified from phase contrast data as the total blood flow to the brain (summation of the mean velocity in each vessel multiplied by the vessel area) normalized to the total tissue volume (gray and white matter). Nonparametric testing was applied to determine differences in study measurements (two-sided significance level=0.05).
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