Cerebral oxygen extraction fraction declines with ventricular enlargement in patients with normal pressure hydrocephalus.

TitleCerebral oxygen extraction fraction declines with ventricular enlargement in patients with normal pressure hydrocephalus.
Publication TypeJournal Article
Year of Publication2023
AuthorsZhuang H, Cho J, Chiang GChia-Yi, Kovanlikaya I, Heier LAnne, Dyke JP, Wang Y
JournalClin Imaging
Volume97
Pagination22-27
Date Published2023 May
ISSN1873-4499
KeywordsBrain, Cerebrovascular Circulation, Gray Matter, Humans, Hydrocephalus, Normal Pressure, Magnetic Resonance Imaging, Neurodegenerative Diseases, Oxygen
Abstract

OBJECTIVE: Normal pressure hydrocephalus (NPH) is a neurodegenerative disease that is potentially reversible by shunt surgery in approximately 60% of patients. Imaging may provide a means to investigate brain tissue viability and oxygen metabolism in NPH patients.

METHODS: Oxygen extraction fraction (OEF) mapping was generated from 3D multi-echo gradient echo MRI (mGRE) data using QQ-CCTV algorithm and cerebral blood flow (CBF) using 3D arterial spin labeling (ASL) MRI data, thereby calculating the cerebral metabolic rate of oxygen (CMRO2 = CBF × OEF × [H]a) in 16 NPH patients. Regression analyses using cortical gray matter and deep gray matter regions were conducted with age, gender, CSF stroke volume and normalized ventricular volume as independent variables.

RESULTS: OEF showed significant negative correlations with normalized brain ventricular volumes in the whole brain (p = 0.004, q = 0.01), cortical gray matter (p = 0.004, q = 0.01), caudate (p = 0.02, q = 0.04), and pallidum (p = 0.03, q = 0.04), but no significant correlation with CSF stroke volume (q > 0.05). There was no significant finding with CBF or CMRO2.

CONCLUSION: In NPH patients, low OEF in several regions was significantly correlated with large ventricular volumes, indicating decreased tissue oxygen metabolism with increased NPH severity. OEF mapping may provide a functional understanding of neurodegeneration in NPH and may improve monitoring of disease course and treatment outcomes.

DOI10.1016/j.clinimag.2023.02.001
Alternate JournalClin Imaging
PubMed ID36871361
PubMed Central IDPMC10081162
Grant ListK99 NS123229 / NS / NINDS NIH HHS / United States
R01 AG068398 / AG / NIA NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI) Brain Health Imaging Institute (BHII)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065