Circadian Blood Pressure Pattern and Microvascular and Macrovascular Cerebral Imaging Burden

Enise Nur Özlem Tiryaki1, Uğur Karagöz2, Muhammet Mücahit Tiryaki3

  • 1Department of Neurology, Yalova Training and Research Hospital, Yalova 77200, Türkiye.

Insights

Reverse dipping blood pressure is linked to more white matter hyperintensity and intracranial arterial calcification. Non-dipping is mainly associated with intracranial arterial calcification, suggesting distinct impacts on cerebral vessels.

Area of Science:

  • Neurology
  • Cardiology
  • Radiology

Background:

  • Nocturnal blood pressure (BP) dipping patterns are linked to cerebrovascular disease.
  • The distinct effects of non-dipping and reverse dipping BP on white matter hyperintensity (WMH) and intracranial arterial calcification (IAC) are not well understood.

Purpose of the Study:

  • To investigate the differential impact of nocturnal BP dipping patterns (dipper, non-dipper, reverse dipper) on WMH burden and IAC.
  • To clarify associations between specific BP dipping phenotypes and neuroimaging markers of cerebrovascular damage.

Main Methods:

  • Retrospective analysis of 376 patients with 24-hour ambulatory BP monitoring, brain MRI, and cranial CT.
  • Patients categorized into dipper (≥10% SBP decline), non-dipper (0-10%), or reverse dipper (<0%) groups.
  • WMH assessed by Fazekas scale; IAC scored as present/absent; multivariable logistic regression used, adjusting for key comorbidities.

Main Results:

  • Reverse dippers showed significantly higher WMH (Fazekas grade) and IAC prevalence compared to dippers.
  • Non-dippers were independently associated with IAC but not WMH.
  • A dose-response trend for IAC was observed across BP dipping categories, with age, diabetes, and CAD as independent IAC predictors.

Conclusions:

  • Reverse dipping is associated with increased WMH burden and IAC.
  • Non-dipping is primarily linked to IAC.
  • Nocturnal BP phenotypes may differentially affect cerebral microvascular and macrovascular imaging markers, warranting further investigation.