Peripheral augmentation index as a biomarker of vascular aging: an invasive hemodynamics approach

Kevin S Heffernan1, Eshan A Patvardhan, Navin K Kapur

  • 1Human Performance Laboratory, Department of Exercise Science, Syracuse University, Syracuse, NY, USA. KsHeffer@syr.edu

Insights

Two non-invasive vascular measures, augmentation index (AIx) and pulse wave amplitude-reactive hyperemia index (PWA-RHI), offer distinct insights into vascular aging. AIx reflects age-related changes and organ damage, while PWA-RHI indicates coronary atherosclerosis burden.

Area of Science:

  • Cardiovascular Medicine
  • Biomedical Engineering
  • Gerontology

Background:

  • Vascular aging is a complex process associated with increased cardiovascular risk.
  • Assessing vascular function non-invasively is crucial for early detection of vascular damage.
  • Digital volume waveform analysis offers novel approaches to evaluate systemic vascular health.

Purpose of the Study:

  • To compare two digital volume waveform-derived measures of vascular function, augmentation index (AIx) and pulse wave amplitude-reactive hyperemia index (PWA-RHI), with invasive measures.
  • To evaluate the relationship of AIx and PWA-RHI with target organ damage and vascular aging parameters.
  • To determine the distinct contributions of AIx and PWA-RHI in assessing systemic vascular health.

Main Methods:

  • Fifty-nine patients undergoing left heart catheterization provided data for invasive vascular function and coronary atherosclerosis assessment (Gensini score).
  • Peripheral arterial tone (PAT) was used to capture digital volume waveforms, from which AIx and PWA-RHI were derived.
  • Statistical analyses correlated AIx and PWA-RHI with age, estimated glomerular filtration rate, left ventricular hypertrophy, and invasive vascular parameters.

Main Results:

  • AIx correlated with age, aortic pulsatility, estimated glomerular filtration rate, aortic pulse pressure amplification, and aortic form factor, and showed a trend towards association with left ventricular hypertrophy.
  • AIx was not associated with the Gensini score, indicating no link to coronary atherosclerotic burden.
  • PWA-RHI was inversely associated with the Gensini score but showed no significant association with age, estimated glomerular filtration rate, or other invasive vascular parameters.

Conclusions:

  • AIx derived from PAT effectively reflects age-associated vascular changes and target organ damage, but not coronary atherosclerotic burden.
  • PWA-RHI is associated with coronary atherosclerotic burden but does not reflect general vascular aging or target organ damage.
  • AIx and PWA-RHI provide complementary information, offering distinct insights into systemic vascular aging and associated organ damage.