NeuroImage · 2023 · 20 citations · 48 references
MedicineNeurologyNeuroscienceClinical NeuroscienceCognitive NeuroscienceDementiaAlzheimer DiseaseCerebral Blood FlowCognitive ImpairmentDementia BiomarkersFunctional NeuroimagingNeuroimaging In DementiaArterial Spin LabelingCerebral Blood Flow AlterationsCerebral Blood Flow QuantificationCerebral Metabolic RateCognitive Status AssessmentOxygen Extraction Fraction ImagingRegional Brain MetabolismRegional Cerebral Blood Flow
The objective of this study was to evaluate the whole-brain pattern of oxygen extraction fraction (OEF), cerebral blood flow (CBF), and cerebral metabolic rate of oxygen consumption (CMRO2) perturbation in Alzheimer's disease (AD) and investigate the relationship between regional cerebral oxygen metabolism and global cognition. Twenty-six AD patients and 25 age-matched healthy controls (HC) were prospectively recruited in this study. Mini-Mental State Examination (MMSE) was used to evaluate cognitive status. We applied QQ-CCTV algorithm which combines quantitative susceptibility mapping and quantitative blood oxygen level-dependent models (QQ) for OEF calculation. CBF map was computed from arterial spin labeling and CMRO2 was generated based on Fick's principle. Whole-brain and regional OEF, CBF, and CMRO2 analyses were performed. The associations between these measures in substructures of deep brain gray matter and MMSE scores were assessed. Whole brain voxel-wise analysis showed that CBF and CMRO2 values significantly decreased in AD predominantly in the bilateral angular gyrus, precuneus gyrus and parieto-temporal regions. Regional analysis showed that CBF value decreased in the bilateral caudal hippocampus and left rostral hippocampus and CMRO2 value decreased in left caudal and rostral hippocampus in AD patients. The mean CBF and CMRO2 values in the bilateral hippocampus positively correlated with the MMSE score over the AD and HC groups combined. CMRO2 mapping with the QQ-CCTV method - which is readily available in MR systems for clinical practice - can be a potential biomarker for AD. In addition, CMRO2 in the hippocampus may be a useful tool for monitoring cognitive impairment.
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