Cerebral vascular shunting and oxygen metabolism in sickle cell disease

Abstract: Patients with sickle cell disease (SCD) are at elevated risk of silent cerebral infarcts and strokes; however, they frequently lack established stroke risk factors (eg, macrovascular arterial steno-occlusion) and the mechanisms underlying such events are incompletely characterized. This st...

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Main Authors: Alexander K. Song, Wesley T. Richerson, Megan A. Aumann, Spencer L. Waddle, R. Sky Jones, Samantha Davis, Lauren Milner, Chelsea Custer, L. Taylor Davis, Sumit Pruthi, Dann Martin, Lori C. Jordan, Manus J. Donahue
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Blood Advances
Online Access:http://www.sciencedirect.com/science/article/pii/S2473952924006566
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author Alexander K. Song
Wesley T. Richerson
Megan A. Aumann
Spencer L. Waddle
R. Sky Jones
Samantha Davis
Lauren Milner
Chelsea Custer
L. Taylor Davis
Sumit Pruthi
Dann Martin
Lori C. Jordan
Manus J. Donahue
author_facet Alexander K. Song
Wesley T. Richerson
Megan A. Aumann
Spencer L. Waddle
R. Sky Jones
Samantha Davis
Lauren Milner
Chelsea Custer
L. Taylor Davis
Sumit Pruthi
Dann Martin
Lori C. Jordan
Manus J. Donahue
author_sort Alexander K. Song
collection DOAJ
description Abstract: Patients with sickle cell disease (SCD) are at elevated risk of silent cerebral infarcts and strokes; however, they frequently lack established stroke risk factors (eg, macrovascular arterial steno-occlusion) and the mechanisms underlying such events are incompletely characterized. This study evaluated cerebral hemometabolism with respect to imaging markers of vascular shunting in 143 participants with SCD, including 73 pediatric (aged 6-17 years) and 70 adult (aged 18-40 years) participants using 3-Tesla brain magnetic resonance imaging (MRI). Vascular shunting was assessed in each patient using a previously published ordinal venous hyperintensity score (VHS) of 0, 1, or 2 on cerebral blood flow-weighted MRI. Participants with VHS of 2, indicative of the most rapid arteriovenous transit, had significantly reduced blood oxygen content (CaO2; 10.90 ± 1.69 mL O2/100 mL blood), oxygen extraction fraction (OEF; 33.52% ± 5.54%), and cerebral metabolic rate of oxygen consumption (CMRO2; 2.91 ± 0.69 mL O2/100 g tissue per minute) compared with their counterparts with VHS = 0 (CaO2 = 12.42 ± 1.58 mL O2/100 mL blood; OEF = 39.03% ± 3.80%; CMRO2 = 3.77 ± 0.84 mL O2/100 g tissue per minute) or VHS = 1 (CaO2 = 11.86 ± 1.73 mL O2/100 mL blood; OEF = 36.37% ± 5.11%; CMRO2 = 3.59 ± 0.78 mL O2/100 g tissue per minute). Both pediatric and adult patients with SCD presenting with greater imaging evidence of vascular shunting had mildly reduced OEF and CMRO2. These findings highlight that imaging markers of vascular shunting are associated with significant, albeit mild, evidence of reduced OEF and CMRO2 in patients with SCD.
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spelling doaj-art-58982659a14d41efa9fbf2eab1d244a22025-01-18T05:04:59ZengElsevierBlood Advances2473-95292025-01-0192386397Cerebral vascular shunting and oxygen metabolism in sickle cell diseaseAlexander K. Song0Wesley T. Richerson1Megan A. Aumann2Spencer L. Waddle3R. Sky Jones4Samantha Davis5Lauren Milner6Chelsea Custer7L. Taylor Davis8Sumit Pruthi9Dann Martin10Lori C. Jordan11Manus J. Donahue12Department of Neurology, Vanderbilt University Medical Center, Nashville, TN; Vanderbilt Brain Institute, Vanderbilt University, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN; Division of Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TNDivision of Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TNDivision of Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN; Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TNDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TNDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TNDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN; Division of Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN; Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TNDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN; Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN; Department of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN; Correspondence: Manus J. Donahue, Behavioral and Cognitive Neurology, Vanderbilt University Medical Center, 1500 21st Ave South Village at Vanderbilt, Suite 2600, Nashville, TN 37212;Abstract: Patients with sickle cell disease (SCD) are at elevated risk of silent cerebral infarcts and strokes; however, they frequently lack established stroke risk factors (eg, macrovascular arterial steno-occlusion) and the mechanisms underlying such events are incompletely characterized. This study evaluated cerebral hemometabolism with respect to imaging markers of vascular shunting in 143 participants with SCD, including 73 pediatric (aged 6-17 years) and 70 adult (aged 18-40 years) participants using 3-Tesla brain magnetic resonance imaging (MRI). Vascular shunting was assessed in each patient using a previously published ordinal venous hyperintensity score (VHS) of 0, 1, or 2 on cerebral blood flow-weighted MRI. Participants with VHS of 2, indicative of the most rapid arteriovenous transit, had significantly reduced blood oxygen content (CaO2; 10.90 ± 1.69 mL O2/100 mL blood), oxygen extraction fraction (OEF; 33.52% ± 5.54%), and cerebral metabolic rate of oxygen consumption (CMRO2; 2.91 ± 0.69 mL O2/100 g tissue per minute) compared with their counterparts with VHS = 0 (CaO2 = 12.42 ± 1.58 mL O2/100 mL blood; OEF = 39.03% ± 3.80%; CMRO2 = 3.77 ± 0.84 mL O2/100 g tissue per minute) or VHS = 1 (CaO2 = 11.86 ± 1.73 mL O2/100 mL blood; OEF = 36.37% ± 5.11%; CMRO2 = 3.59 ± 0.78 mL O2/100 g tissue per minute). Both pediatric and adult patients with SCD presenting with greater imaging evidence of vascular shunting had mildly reduced OEF and CMRO2. These findings highlight that imaging markers of vascular shunting are associated with significant, albeit mild, evidence of reduced OEF and CMRO2 in patients with SCD.http://www.sciencedirect.com/science/article/pii/S2473952924006566
spellingShingle Alexander K. Song
Wesley T. Richerson
Megan A. Aumann
Spencer L. Waddle
R. Sky Jones
Samantha Davis
Lauren Milner
Chelsea Custer
L. Taylor Davis
Sumit Pruthi
Dann Martin
Lori C. Jordan
Manus J. Donahue
Cerebral vascular shunting and oxygen metabolism in sickle cell disease
Blood Advances
title Cerebral vascular shunting and oxygen metabolism in sickle cell disease
title_full Cerebral vascular shunting and oxygen metabolism in sickle cell disease
title_fullStr Cerebral vascular shunting and oxygen metabolism in sickle cell disease
title_full_unstemmed Cerebral vascular shunting and oxygen metabolism in sickle cell disease
title_short Cerebral vascular shunting and oxygen metabolism in sickle cell disease
title_sort cerebral vascular shunting and oxygen metabolism in sickle cell disease
url http://www.sciencedirect.com/science/article/pii/S2473952924006566
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