Near-infrared spectroscopy provides an affordable, versatile, and noninvasive technique for evaluating mitochondrial oxidative capacity of skeletal muscle in clinical populations.
Can near-infrared spectroscopy (NIRS) be used to noninvasively evaluate skeletal muscle mitochondrial dysfunction in clinical populations?
NIRS is a versatile, noninvasive, and economical tool for evaluating skeletal muscle mitochondrial oxidative capacity in clinical populations, offering an alternative to muscle biopsies and 31P MRS.
The ability to sustain submaximal exercise is largely dependent on the oxidative capacity of mitochondria within skeletal muscle, and impairments in oxidative metabolism have been implicated in many neurologic and cardiovascular pathologies. Here we review studies which have demonstrated the utility of Near-infrared spectroscopy (NIRS) as a method of evaluating of skeletal muscle mitochondrial dysfunction in clinical human populations. Near-infrared spectroscopy (NIRS) has been previously used to noninvasively measure tissue oxygen saturation in humans, but recent studies have demonstrated the utility of NIRS as a method of evaluating skeletal muscle oxidative capacity using post-exercise recovery kinetics of oxygen metabolism. In comparison to historical methods of measuring muscle metabolic dysfunction in vivo, NIRS provides a more versatile and economical method of evaluating mitochondrial oxidative capacity in humans. These advantages generate great potential for the clinical applicability of NIRS as a means of evaluating muscle dysfunction in clinical populations.
Willingham et al. (Thu,) conducted a review in Mitochondrial dysfunction in neurological, cardiovascular, respiratory, and mitochondrial diseases. Near-Infrared Spectroscopy (NIRS) vs. Standard assessment methods (e.g., 31P MRS, muscle biopsies) or healthy controls was evaluated on Skeletal muscle mitochondrial oxidative capacity. Near-infrared spectroscopy provides an affordable, versatile, and noninvasive technique for evaluating mitochondrial oxidative capacity of skeletal muscle in clinical populations.