Abstract
Physiological interactions are abundant within, and between, body systems. These interactions may evolve into discrete states during pathophysiological processes resulting from common mechanisms. An association between arterial stenosis, identified by low ankle-brachial pressure index (ABPI) and cardiovascular disease (CVD) as been reported. Whether an association between vascular calcification-characterized by high ABPI and a different pathophysiology-is similarly associated with CVD, has not been established. The current study aims to investigate the association between ABPI, and cardiac rhythm, as an indicator of cardiovascular health and functionality, utilizing heart rate variability (HRV). Two hundred and thirty six patients underwent ABPI assessment. Standard time and frequency domain, and non-linear HRV measures were determined from 5-min electrocardiogram. ABPI data were divided into normal (n = 101), low (n = 67) and high (n = 66) and compared to HRV measures.(DFAα1 and SampEn were significantly different between the low ABPI, high ABPI and control groups (p < 0.05). A possible coupling between arterial stenosis and vascular calcification with decreased and increased HRV respectively was observed. Our results suggest a model for interpreting the relationship between vascular pathophysiology and cardiac rhythm. The cardiovascular system may be viewed as a complex system comprising a number of interacting subsystems. These cardiac and vascular subsystems/networks may be coupled and undergo transitions in response to internal or external perturbations. From a clinical perspective, the significantly increased sample entropy compared to the normal ABPI group and the decreased and increased complex correlation properties measured by DFA for the low and high ABPI groups respectively, may be useful indicators that a more holistic treatment approach in line with this more complex clinical picture is required.
Highlights
The evolution of complex systems may be characterized by nonequilibrium phase transitions that lead to a divergence of structure and function in biological systems (Haken, 1983)
The current results show that DFAα1 was decreased in the low ankle-brachial pressure index (ABPI) group, as compared to the normal ABPI group, indicting a loss of complexity in heart rate variability (HRV) associated with arterial stenosis
Our current findings demonstrate that the relationship between heart rate variability, as an indicator of cardiac rhythm, and ABPI depends on whether Peripheral vascular disease (PVD) is defined as arterial stenosis or vascular calcification
Summary
The evolution of complex systems may be characterized by nonequilibrium phase transitions that lead to a divergence of structure and function in biological systems (Haken, 1983). ABPI values range from 0.5 to above 1.4 indicating either arterial stenosis or vascular calcification (Jelinek and Austin, 2006) This divergent pathophysiology hinges on changes in metabolic processes such as oxidative stress (Loffredo et al, 2007), where increased reactive oxygen species (ROS) have been shown to have a causative role in atherosclerosis and vessel narrowing, leading to a lower ABPI (Dröge, 2002; Madamanchi et al, 2005). The autonomic nervous system, which, regulates heart rate and vessel diameter, is affected by ROS through central or peripheral mechanisms (Feldman, 2003; Ye et al, 2006) These neural processes may be coupled to different pathological stable states such as arterial stenosis and vascular calcification (Figure 1). The current study aims to investigate the association between ABPI, and cardiac rhythm, as an indicator of cardiovascular health and functionality, utilizing heart rate variability (HRV)
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