Comparison of non-invasive MRI measurements of cerebral blood flow in a large multisite cohort

Author:

Dolui Sudipto123,Wang Ze45,Wang Danny JJ6,Mattay Raghav7,Finkel Mack8,Elliott Mark1,Desiderio Lisa1,Inglis Ben9,Mueller Bryon10,Stafford Randall B11,Launer Lenore J12,Jacobs David R13,Bryan R Nick1,Detre John A123

Affiliation:

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

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

3. Center for Functional Neuroimaging, University of Pennsylvania, Philadelphia, PA, USA

4. Center for Cognition and Brain Disorders and the Affiliated Hospital, Hangzhou Normal University, Hangzhou, China

5. Departments of Psychiatry and Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

6. Department of Neurology, University of California, Los Angeles, CA, USA

7. Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

8. School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA, USA

9. Henry H. Wheeler Jr. Brain Imaging Center, University of California, Berkeley, CA, USA

10. 0Department of Psychiatry, University of Minnesota, Minneapolis, MN, USA

11. 1Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada

12. 2Laboratory of Epidemiology and Population Science, National Institute on Aging, Bethesda, MD, USA

13. 3Division of Epidemiology and Community Health, University of Minnesota, Minneapolis, MN, USA

Abstract

Arterial spin labeling and phase contrast magnetic resonance imaging provide independent non-invasive methods for measuring cerebral blood flow. We compared global cerebral blood flow measurements obtained using pseudo-continuous arterial spin labeling and phase contrast in 436 middle-aged subjects acquired at two sites in the NHLBI CARDIA multisite study. Cerebral blood flow measured by phase contrast (CBFPC: 55.76 ± 12.05 ml/100 g/min) was systematically higher ( p < 0.001) and more variable than cerebral blood flow measured by pseudo-continuous arterial spin labeling (CBFPCASL: 47.70 ± 9.75). The correlation between global cerebral blood flow values obtained from the two modalities was 0.59 ( p < 0.001), explaining less than half of the observed variance in cerebral blood flow estimates. Well-established correlations of global cerebral blood flow with age and sex were similarly observed in both CBFPCASL and CBFPC. CBFPC also demonstrated statistically significant site differences, whereas no such differences were observed in CBFPCASL. No consistent velocity-dependent effects on pseudo-continuous arterial spin labeling were observed, suggesting that pseudo-continuous labeling efficiency does not vary substantially across typical adult carotid and vertebral velocities, as has previously been suggested. Conclusions: Although CBFPCASL and CBFPC values show substantial similarity across the entire cohort, these data do not support calibration of CBFPCASL using CBFPC in individual subjects. The wide-ranging cerebral blood flow values obtained by both methods suggest that cerebral blood flow values are highly variable in the general population.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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