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Parkinson's disease cerebrovascular reactivity pattern: A feasibility study. | LitMetric

AI Article Synopsis

  • Research indicates cerebrovascular dysfunction plays a key role in Parkinson's disease (PD), prompting a study using BOLD MRI to assess cerebrovascular reactivity (CVR) in PD patients compared to healthy controls.
  • The study analyzed whole-brain maps of CVR amplitude and latency, revealing a specific pattern (PD-CVRP) with increased latency in several brain areas for PD patients and decreased latency in cerebral white matter.
  • While no significant clinical correlations were identified due to sample size limitations, the PD-CVRP underscores the potential of cerebrovascular dysfunction as a biomarker for PD in future research.

Article 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 CO) 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11494834PMC
http://dx.doi.org/10.1177/0271678X241241895DOI Listing

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