The Hyperintense study: Assessing the effects of induced blood pressure increase and decrease on MRI markers of

Esther Janssen1,2, Annemieke Ter Telgte3, Esmée Verburgt1,2

  • 1Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

European Stroke Journal
|September 9, 2022
PubMed

Insights

This study investigates how blood pressure changes affect cerebral small vessels in hypertensive adults. Understanding these mechanisms could lead to new treatments for small vessel disease (SVD).

Area of Science:

  • Neurology
  • Cardiovascular Research
  • Medical Imaging

Background:

  • Cerebral small vessel disease (SVD) is common in older adults, but its causes are unclear.
  • Hypertension is a risk factor for SVD, yet direct causal links remain unknown.
  • The Hyperintense study examines early cerebrovascular changes in young hypertensive adults.

Purpose of the Study:

  • To investigate the pathophysiological mechanisms linking hypertension to SVD.
  • To assess the effects of blood pressure fluctuations on cerebral small vessels.
  • To identify potential new therapeutic targets for SVD prevention and treatment.

Main Methods:

  • Prospective observational cohort study of 50 hypertensive adults (aged 18-55).
  • Temporary discontinuation of antihypertensive medication to induce blood pressure changes.
  • Multi-timepoint 3T MRI (including DCE-MRI, white matter integrity, microperfusion) and clinical assessments.

Main Results:

  • Data collection at four timepoints: baseline, medication withdrawal, medication restart, and 1-year follow-up.
  • Assessment of blood-brain barrier function, white matter integrity, and microperfusion.
  • Correlation of blood pressure changes with neuroimaging markers of SVD.

Conclusions:

  • The study aims to elucidate the early stages of SVD development in hypertension.
  • Findings may reveal novel therapeutic strategies for managing SVD.
  • Improved understanding of hypertension's impact on cerebral microvasculature.
Abstract