Parkinson’s disease cerebrovascular reactivity pattern: A feasibility study

Author:

van der Horn Harm Jan1,Vakhtin Andrei A1,Julio Kayla1,Nitschke Stephanie1,Shaff Nicholas1,Dodd Andrew B1,Erhardt Erik2,Phillips John P1,Pirio Richardson Sarah34,Deligtisch Amanda3,Stewart Melanie3,Suarez Cedeno Gerson3,Meles Sanne K5,Mayer Andrew R1,Ryman Sephira G13

Affiliation:

1. Department of Translational Neuroscience, The Mind Research Network, Albuquerque, NM, USA

2. Department of Mathematics and Statistics, University of New Mexico, Albuquerque, NM, USA

3. Nene and Jamie Koch Comprehensive Movement Disorder Center, Department of Neurology, University of New Mexico, Albuquerque, NM, USA

4. New Mexico VA Health Care System, Albuquerque, NM, USA

5. Department of Neurology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

Abstract

A mounting body of research points to cerebrovascular dysfunction as a fundamental element in the pathophysiology of Parkinson’s disease (PD). In the current feasibility study, blood-oxygen-level-dependent (BOLD) MRI was used to measure cerebrovascular reactivity (CVR) in response to hypercapnia in 26 PD patients and 16 healthy controls (HC), and aimed to find a multivariate pattern specific to PD. Whole-brain maps of CVR amplitude (i.e., magnitude of response to CO2) and latency (i.e., time to reach maximum amplitude) were computed, which were further analyzed using scaled sub-profile model principal component analysis (SSM-PCA) with leave-one-out cross-validation. A meaningful pattern based on CVR latency was identified, which was named the PD CVR pattern (PD-CVRP). This pattern was characterized by relatively increased latency in basal ganglia, sensorimotor cortex, supplementary motor area, thalamus and visual cortex, as well as decreased latency in the cerebral white matter, relative to HC. There were no significant associations with clinical measures, though sample size may have limited our ability to detect significant associations. In summary, the PD-CVRP highlights the importance of cerebrovascular dysfunction in PD, and may be a potential biomarker for future clinical research and practice.

Publisher

SAGE Publications

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