Racial differences in arterial stiffness and microcirculatory function between Black and White Americans

Alanna A Morris1, Riyaz S Patel, Jose Nilo G Binongo

  • 1Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA. aamorr3@emory.edu

Insights

Black Americans exhibit impaired vascular function, including reduced microvascular endothelial function and increased arterial stiffness and wave reflections, contributing to higher cardiovascular disease risk.

Area of Science:

  • Cardiovascular Science
  • Vascular Biology
  • Racial Health Disparities

Background:

  • Black Americans experience a disproportionately high burden of cardiovascular disease (CVD).
  • Racial disparities in CVD prevalence may stem from underlying differences in vascular function.

Purpose of the Study:

  • To investigate racial differences in vascular function between Black and White individuals.
  • To determine if impaired vascular function in Black individuals persists after accounting for traditional cardiovascular disease risk factors.

Main Methods:

  • Vascular function was assessed in 385 Black and 470 White subjects using digital pulse amplitude tonometry (EndoPAT) and applanation tonometry (Sphygmocor).
  • Key measures included reactive hyperemia index (RHI) for microvascular endothelial function, augmentation index (PAT-AIx, C-AIx) for arterial wave reflections, and pulse-wave velocity (PWV) for arterial stiffness.

Main Results:

  • Black individuals had significantly lower RHI, greater PAT-AIx and C-AIx, and higher PWV compared to White individuals.
  • These associations remained significant after adjusting for traditional CVD risk factors.
  • Impaired vascular function was observed even in healthy Black individuals without traditional CVD risk factors.

Conclusions:

  • Black race is independently associated with impaired microvascular endothelial function, increased arterial wave reflections, and greater arterial stiffness.
  • These vascular impairments may represent key mechanisms underlying the elevated CVD risk observed in Black populations.
Abstract