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analysis of the blood flux signals has begun to shed new light on the flexibility of the
system in response to standard haemodynamic perturbations and in human cohorts
at increasing risk and severity of cardiovascular and metabolic disease. Nonlinear
complexity methods have been used to quantify the regularity of the blood flux signal
by evaluating the presence of repeated patterns, providing complexity variants at
single and across multiple spatial and temporal scales. Further, the new approach of
attractor reconstruction analysis offers quantitative measures of the microvascular
system in phase space and a visual representation in the shape and variability of
the signal producing a two-dimensional attractor with features such as density and
symmetry. Nonlinear analysis thus provides a better characterisation of the flexibility
of the system in a range of pathophysiological conditions.
In conclusion, these mathematical approaches are able to identify changes in
microvascular function and have utility in understanding the fundamental mechanistic contributors to microvascular (dys)function. To what extent they can be used
to discriminate between (patho)physiological states and in the understanding of the
effectiveness of interventions for reversing established vasculopathy and perfusion
impairments has yet to be determined. They have yet to be used to inform treatment
regimens or to predict clinical outcomes. With machine learning techniques these
novel approaches may, in future, support a more effective and mechanism-based
classification of tissue perfusion, providing a use in clinical assessment.
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