Elevated augmentation index derived from peripheral arterial tonometry is associated with abnormal ventricular-vascular coupling
Elevated augmentation index derived from peripheral arterial tonometry is associated with abnormal ventricular-vascular coupling
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DOI:
10.1111/j.1475-097x.2010.00943.x
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发表时间:
2010-09-01
影响因子:
1.8
通讯作者:
Kuvin, Jeffrey T.
中科院分区:
文献类型:
--
作者:
Heffernan, Kevin S.;Patvardhan, Eshan A.;Kuvin, Jeffrey T.
P>Background:Although typically derived from the contour of arterial pressure waveform, augmentation index (AIx) may also be derived from the digital pulse volume waveform using finger plethysmography (peripheral arterial tonometry, PAT). Little is known regarding the physiologic correlates of AIx derived from PAT. In this study, we investigated the relation of PAT-AIx with measures of ventricular-vascular coupling.Methods:Pulse volume waves were measured via PAT and used to derive AIx. Using 2-dimensional echocardiography, effective arterial elastance index (EaI) was estimated as end-systolic pressure/stroke volume index. Left ventricular (LV) end-systolic elastance index (ELVI) was calculated as end-systolic pressure/end-systolic volume index. Ventricular-vascular coupling ratio was defined as EaI/ELVI.Results:Given the bi-directional nature of ventricular-vascular uncoupling as measured by echocardiography, patients were separated into three groups: low EaI/ELVI (< 0 center dot 6, n = 21), optimal EaI/ELVI (mean 0 center dot 6-1 center dot 2, n = 16) and high EaI/ELVI (> 1 center dot 2, n = 10). Adjusting for potential confounders (age, mean arterial pressure, height and heart rate), patients with optimal EaI/ELVI had lower AIx (1 +/- 4%, P < 0 center dot 05) compared to those with low EaI/ELVI (13 +/- 4%) and high EaI/ELVI (19 +/- 5%).Conclusions:Abnormal ventricular-vascular coupling, arising from either increased effective arterial elastance or increased ventricular elastance, is associated with increased AIx as measured by PAT. Additional research is needed to examine other vascular correlates of PAT-AIx.