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Published on: August 21, 2017
Altered neurovascular coupling in neuromyelitis optica
Xi Guo1, Jiajia Zhu2, Ningnannan Zhang1
1Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin, China.
Neurovascular coupling is altered in neuromyelitis optica (NMO), impacting cognitive decline. This study reveals abnormal brain blood flow and neuronal activity relationships in NMO patients, linking them to disease severity.
Area of Science:
- Neuroscience
- Radiology
- Immunology
Background:
- Neurovascular coupling links neuronal activity and cerebral blood flow (CBF), crucial for brain function.
- Neuromyelitis optica (NMO) is an autoimmune disease affecting the central nervous system, often leading to cognitive decline.
- Existing research highlights gray matter abnormalities in NMO but lacks detailed understanding of neurovascular coupling.
Purpose of the Study:
- To investigate alterations in neurovascular coupling in NMO patients.
- To explore the clinical significance of these neurovascular coupling changes.
- To correlate neurovascular coupling abnormalities with disease severity and cognitive impairment.
Main Methods:
- Used functional MRI for regional homogeneity (ReHo) to assess neuronal activity.
- Employed arterial spin labeling (ASL) to measure cerebral blood flow (CBF).
- Analyzed global CBF-ReHo correlations and regional CBF/ReHo ratios in 56 NMO patients and 63 controls.
Main Results:
- Global neurovascular coupling (CBF-ReHo correlation) was significantly decreased in NMO patients.
- Regional CBF/ReHo ratios showed decreased values in parietal/occipital lobes and increased values in insular/sensorimotor/temporal/prefrontal regions.
- These regional abnormalities were often undetectable by analyzing CBF or ReHo alone.
Conclusions:
- NMO patients exhibit widespread neurovascular coupling dysfunction.
- Abnormalities in neurovascular coupling are associated with more severe clinical impairments and cognitive decline in NMO.
- Assessing neurovascular coupling provides deeper insights into NMO pathophysiology beyond individual CBF or ReHo measures.
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