Blunt Cardiovascular Response to Active Standing in Patients with Intracranial Atherosclerotic Stenosis

Yufan Cao1, Yuexuan Dai1, Jiaxin Liu2

  • 1Department of Neurology, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital/Peking Union Medical College, Beijing, China.

Insights

Patients with intracranial atherosclerotic stenosis (ICAS) show blunted cerebral blood flow (CBF) responses to standing. This impaired CBF regulation is partly mediated by reduced heart rate variability (HRV), suggesting a heart-brain connection.

Area of Science:

  • Neurology
  • Cardiology
  • Vascular Medicine

Background:

  • Intracranial atherosclerotic stenosis (ICAS) affects cerebral blood flow (CBF) dynamics.
  • Active standing simulates rapid blood pressure fluctuations, revealing physiological responses.
  • Investigating the interplay between CBF and heart rate (HR) in ICAS is crucial.

Purpose of the Study:

  • To examine dynamic changes in CBF and HR during active standing in ICAS patients.
  • To assess the interconnectivity of CBF and HR responses in relation to stenosis.
  • To explore the role of heart rate variability (HRV) in mediating these responses.

Main Methods:

  • Cross-sectional analysis within a prospective cohort.
  • Transcranial Doppler monitoring of 302 middle cerebral arteries in 182 subjects.
  • Comparison of CBF velocity and HR trends during supine to active standing transitions.

Main Results:

  • CBF velocity showed a decrease then rebound upon standing; rebound time was prolonged in stenotic arteries.
  • Patients with ICAS exhibited lower maximum HR rangeability and a trend towards lower HRV.
  • HRV partially mediated the effect of stenosis on prolonged CBF velocity rebound time (12.76% mediation).

Conclusions:

  • Cerebral blood flow in stenotic arteries demonstrates a blunted response to blood pressure fluctuations.
  • Reduced HRV may contribute to impaired CBF regulation in ICAS.
  • Heart rate monitoring may aid in managing ICAS-related cerebral hypoperfusion.
Abstract

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