Near-infrared spectroscopy offers a non-invasive, 'one stop shop' approach to evaluate key microvascular and oxidative endpoints, providing mechanistic insights into exercise intolerance and cardiovascular dysfunction.
Answers are grounded in this paper and cite their sources.
Enables efficient microvascular phenotyping in research; leaves open clinical validation before practice adoption.
Exercise represents a major hemodynamic stress that demands a highly coordinated neurovascular response in order to match oxygen delivery to metabolic demand. Reactive hyperemia (in response to a brief period of tissue ischemia) is an independent predictor of cardiovascular events and provides important insight into vascular health and vasodilatory capacity. Skeletal muscle oxidative capacity is equally important in health and disease, as it determines the energy supply for myocellular processes. Here, we describe a simple, non-invasive approach using near-infrared spectroscopy to assess each of these major clinical endpoints (reactive hyperemia, neurovascular coupling, and muscle oxidative capacity) during a single clinic or laboratory visit. Unlike Doppler ultrasound, magnetic resonance images/spectroscopy, or invasive catheter-based flow measurements or muscle biopsies, our approach is less operator-dependent, low-cost, and completely non-invasive. Representative data from our lab taken together with summary data from previously published literature illustrate the utility of each of these end-points. Once this technique is mastered, application to clinical populations will provide important mechanistic insight into exercise intolerance and cardiovascular dysfunction.
No takes yet. Share an insight, caveat, or question.
Rosenberry et al. (2018) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: