MRI evaluation of cerebral metabolic rate of oxygen (CMRO2) in obstructive sleep apnea

Author:

Wu Pei-Hsin12ORCID,Rodríguez-Soto Ana E1,Wiemken Andrew3,Englund Erin K1,Rodgers Zachary B1,Langham Michael C1,Schwab Richard J3,Detre John A4,Guo Wensheng5,Wehrli Felix W1

Affiliation:

1. Department of Radiology, University of Pennsylvania, University of Pennsylvania, Philadelphia, PA, USA

2. Department of Electrical Engineering, National Sun Yat-sen University, National Sun Yat-sen University, Kaohsiung, Taiwan

3. Division of Sleep Medicine, Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA

4. Department of Neurology, University of Pennsylvania, Philadelphia, PA, USA

5. Department of Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA, USA

Abstract

Patients with obstructive sleep apnea (OSA) are at elevated risk of developing systemic vascular disease and cognitive dysfunction. Here, cerebral oxygen metabolism was assessed in patients with OSA by means of a magnetic resonance-based method involving simultaneous measurements of cerebral blood flow rate and venous oxygen saturation in the superior sagittal sinus for a period of 10 minutes at an effective temporal resolution of 1.3 seconds before, during, and after repeated 24-second breath-holds mimicking spontaneous apneas, yielding, along with pulse oximetry-derived arterial saturation, whole-brain CMRO2 via Fick’s Principle. Enrolled subjects were classified based on their apnea-hypopnea indices into OSA (N = 31) and non-sleep apnea reference subjects (NSA = 21), and further compared with young healthy subjects (YH, N = 10). OSA and NSA subjects were matched for age and body mass index. CMRO2 was lower in OSA than in the YH group during normal breathing (105.6 ± 14.1 versus 123.7 ± 22.8 μmol O2/min/100g, P = 0.01). Further, the fractional change in CMRO2 in response to a breath-hold challenge was larger in OSA than in the YH group (15.2 ± 9.2 versus 8.5 ± 3.4%, P = 0.04). However, there was no significant difference in CMRO2 between OSA and NSA subjects. The data suggest altered brain oxygen metabolism in OSA and possibly in NSA as well.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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