Reduced blood oxygenation level dependent connectivity is related to hypoperfusion in Alzheimer’s disease

Author:

Göttler Jens12ORCID,Preibisch Christine123ORCID,Riederer Isabelle12,Pasquini Lorenzo24,Alexopoulos Panagiotis5,Bohn Karl Peter6,Yakushev Igor26,Beller Ebba7,Kaczmarz Stephan12,Zimmer Claus1,Grimmer Timo25,Drzezga Alexander68,Sorg Christian125

Affiliation:

1. Department of Diagnostic and Interventional Neuroradiology, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany

2. TUM Neuroimaging Center (TUM-NIC), Klinikum Rechts der Isar, Technische Universität München, Munich, Germany

3. Clinic for Neurology, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany

4. Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA, USA

5. Department of Psychiatry and Psychotherapy, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany

6. Department of Nuclear Medicine, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany

7. Department of Radiology, Klinikum Großhadern, Ludwig-Maximilans-Universität München, Munich, Germany

8. Department of Nuclear Medicine, University of Cologne, Cologne, Germany

Abstract

Functional connectivity of blood oxygenation level dependent signal fluctuations (BOLD-FC) is decreased in Alzheimer’s disease (AD), and suggested to reflect reduced coherence in neural population activity; however, as both neuronal and vascular-hemodynamic processes underlie BOLD signals, impaired perfusion might also contribute to reduced BOLD-FC; 42 AD patients and 27 controls underwent simultaneous PET/MR imaging. Resting-state functional MRI assessed BOLD co-activity to quantify BOLD-FC, pulsed arterial spin labeling (pASL) assessed cerebral blood flow (CBF) as proxy for vascular hemodynamics, and 18F-fluorodeoxyglucose PET assessed glucose metabolism (GluMet) to index neuronal activity. Patients’ BOLD-FC, CBF, and GluMet were reduced within the same precuneal parietal regions. BOLD-FC was positively associated with mean CBF, specifically in patients and controlled for GluMet levels, suggesting that BOLD-FC reductions correlate with pASL-derived hypoperfusion in AD, independently from 18F-fluorodeoxyglucose PET-derived hypometabolism. Data indicate that impaired vascular hemodynamic processes contribute to reduced BOLD connectivity in AD.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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