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September 17, 2025Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition0 citations

Estimation of Cerebral Oxygen Extraction Fraction (OEF) by Haematocrit-Corrected QQ (QSM + qBOLD) in Sickle Cell Anaemia

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IHIan HawleyConquest HospitalMLM.C. LeeNational Yang Ming Chiao Tung UniversityHSHanne StotesburyThe King's College

Key Points

  • Participants with sickle cell anaemia had significantly higher oxygen extraction fraction compared to controls.
  • Cerebral metabolic rate of oxygen consumption was notably elevated in white matter of children with sickle cell anaemia.
  • The study employed a non-invasive MRI technique combining QSM and qBOLD to measure cerebral blood flow.
  • These findings underline the crucial link between cerebral metabolism and tissue injury in sickle cell anaemia.

Abstract

Motivation: Cerebral injury in Sickle cell anaemia (SCA) is hypothesised to be caused by an inability to maintain stable oxygen delivery to tissue. A biomarker of tissue vulnerability is the cerebral metabolic rate of oxygen consumption (CMRO2). Goal(s): Estimate regional Oxygen Extraction fraction (OEF) and CMRO2 in participants with SCA and healthy controls using non-invasive regional MRI. Approach: QQ (QSM + qBOLD) was used to estimate voxel-wise OEF - enabling calculation of regional CMRO2. Results: SCA participants had significantly higher cerebral blood flow and OEF compared to controls. CMRO2 was higher in white matter in children, but not adults, with SCA. Impact: QQ (QSM + qBOLD) enables a non-invasive method of studying haemodynamic health via regional estimation of OEF and CMRO2 in participants, of all ages, with SCA. The differences found suggest the important role of cerebral metabolism in tissue injury.

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Cite This Study

Hawley et al. (2025) studied this question.

synapsesocial.com/papers/68d4597b31b076d99fa5cb78https://doi.org/10.58530/2025/0718
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