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Updated: Feb 28, 2026

Cerebral Blood Flow-Based Resting State Functional Connectivity of the Human Brain using Optical Diffuse Correlation Spectroscopy
Published on: May 27, 2020
Resting-State Cerebral Blood Flow and Its Disconnect From Functional Connectivity in Alzheimer's Disease Spectrum
Xiao Su1, Yu Wang2, Baomin Zhao3
1Department of Neurology (XS, YW, BZ, CW, QL, YZ, FL, PC, NZ), Tianjin Medical University General Hospital, Tianjin, China; Department of Neurology (XS), The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.
Neurovascular decoupling is evident in early Alzheimer's disease (AD), worsening with progression. The cerebral blood flow to functional connectivity strength (CBF/FCS) ratio may serve as an early diagnostic biomarker for AD.
Area of Science:
- Neuroscience
- Neurology
- Medical Imaging
Background:
- Neurovascular coupling disruption is linked to Alzheimer's disease (AD) pathogenesis.
- Early changes in symptomatic AD patients require further clarification.
Purpose of the Study:
- To investigate neurovascular coupling in early Alzheimer's disease.
- To assess the utility of the cerebral blood flow to functional connectivity strength (CBF/FCS) ratio as a biomarker.
Main Methods:
- Studied 50 AD patients, 38 mild cognitive impairment (MCI) patients, and 50 controls.
- Utilized whole-brain functional connectivity strength (FCS) and cerebral blood flow (CBF) maps.
- Assessed global neurovascular coupling via CBF-FCS correlation and regional coupling via CBF/FCS ratio.
Main Results:
- Overall neurovascular coupling (CBF-FCS) declined gradually in AD patients compared to controls.
- Reduced regional CBF/FCS ratio observed in temporal and angular gyri in AD patients.
- Regional CBF/FCS in the inferior temporal gyrus correlated positively with visuospatial function in AD dementia.
Conclusions:
- Neurovascular decoupling is present in early AD and progresses with the disease.
- The CBF/FCS ratio shows potential as a biomarker for early AD diagnosis and clinical assessment.
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