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Updated: May 2, 2026

Author Spotlight: Noninvasive Cerebral Blood Flow Determination in Human Functional Brain Region for Diagnosis of Neurological Disorders
Published on: May 31, 2024
Hydrocephalus decreases arterial spin-labeled cerebral perfusion
K W Yeom1, R M Lober2, A Alexander2
1From the Departments of Radiology (K.W.Y.) kyeom@stanford.edu.
Insights
Arterial spin-labeled cerebral blood flow (CBF) was reduced in children with hydrocephalus and improved after treatment. This perfusion imaging may help monitor intracranial pressure noninvasively.
Area of Science:
- Neuroimaging
- Pediatric Neurology
- Cerebrovascular Physiology
Background:
- Elevated intracranial pressure is linked to reduced cerebral perfusion.
- Arterial spin-labeling (ASL) is a non-invasive MRI technique to measure cerebral blood flow (CBF).
Purpose of the Study:
- To evaluate arterial spin-labeling CBF as a potential marker for symptomatic hydrocephalus in children.
- To assess the relationship between ASL-CBF and ventricular size.
- To determine if ASL-CBF changes after hydrocephalus alleviation.
Main Methods:
- Compared ASL-CBF in children with posterior fossa tumors and intracranial hypertension to controls.
- Measured ASL-CBF in the cerebrum, deep gray nuclei, and periventricular white matter.
- Assessed ASL-CBF changes before and after hydrocephalus treatment in symptomatic patients.
Main Results:
- Children with uncompensated hydrocephalus showed significantly lower ASL-CBF in all brain regions compared to controls.
- ASL-CBF increased significantly after alleviation of hydrocephalus.
- A greater distance between frontal horns correlated with lower cerebral ASL-CBF.
Conclusions:
- ASL-CBF is reduced in children with uncompensated hydrocephalus.
- ASL-CBF normalizes after hydrocephalus treatment, indicating its responsiveness.
- ASL-CBF perfusion MRI shows promise as a non-invasive tool for monitoring hydrocephalus and intracranial pressure.
Background And Purpose:
Reduced cerebral perfusion has been observed with elevated intracranial pressure. We hypothesized that arterial spin-labeled CBF can be used as a marker for symptomatic hydrocephalus.
Materials And Methods:
We compared baseline arterial spin-labeled CBF in 19 children (median age, 6.5 years; range, 1-17 years) with new posterior fossa brain tumors and clinical signs of intracranial hypertension with arterial spin-labeled CBF in 16 age-matched controls and 4 patients with posterior fossa tumors without ventriculomegaly or signs of intracranial hypertension. Measurements were recorded in the cerebrum at the vertex, deep gray nuclei, and periventricular white matter and were assessed for a relationship to ventricular size. In 16 symptomatic patients, we compared cerebral perfusion before and after alleviation of hydrocephalus.
Results:
Patients with uncompensated hydrocephalus had lower arterial spin-labeled CBF than healthy controls for all brain regions interrogated (P < .001). No perfusion difference was seen between asymptomatic patients with posterior fossa tumors and healthy controls (P = 1.000). The median arterial spin-labeled CBF increased after alleviation of obstructive hydrocephalus (P < .002). The distance between the frontal horns inversely correlated with arterial spin-labeled CBF of the cerebrum (P = .036) but not the putamen (P = .156), thalamus (P = .111), or periventricular white matter (P = .121).
Conclusions:
Arterial spin-labeled-CBF was reduced in children with uncompensated hydrocephalus and restored after its alleviation. Arterial spin-labeled-CBF perfusion MR imaging may serve a future role in the neurosurgical evaluation of hydrocephalus, as a potential noninvasive method to follow changes of intracranial pressure with time.
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