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May 11, 2012Journal of Applied Physiology236 citationsOpen Access

Noninvasive evaluation of skeletal muscle mitochondrial capacity with near-infrared spectroscopy: correcting for blood volume changes

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TRTerence E. RyanMEMelissa L. EricksonJBJared T. Brizendine

Structured PICO

Does blood volume-corrected NIRS reliably and reproducibly measure skeletal muscle mitochondrial capacity in human subjects?

P
Population
24 subjects, including 4 with chronic spinal cord injury and 10 healthy able-bodied subjects
I
Intervention
Near-infrared spectroscopy (NIRS) with blood volume correction and ischemic calibration
C
Comparator
Uncorrected NIRS signals (absolute units)
O
Outcome
Reliability and reproducibility of NIRS measurements of resting oxygen consumption and mitochondrial capacitysurrogate

Blood volume-corrected NIRS signals provide a reliable and reproducible noninvasive method to assess in vivo skeletal muscle oxidative capacity.

Abstract

Near-infrared spectroscopy (NIRS) is a well-known method used to measure muscle oxygenation and hemodynamics in vivo. The application of arterial occlusions allows for the assessment of muscle oxygen consumption (mVo(2)) using NIRS. The aim of this study was to measure skeletal muscle mitochondrial capacity using blood volume-corrected NIRS signals that represent oxygenated hemoglobin/myoglobin (O(2)Hb) and deoxygenated hemoglobin/myoglobin (HHb). We also assessed the reliability and reproducibility of NIRS measurements of resting oxygen consumption and mitochondrial capacity. Twenty-four subjects, including four with chronic spinal cord injury, were tested using either the vastus lateralis or gastrocnemius muscles. Ten healthy, able-bodied subjects were tested on two occasions within a period of 7 days to assess the reliability and reproducibility. NIRS signals were corrected for blood volume changes using three different methods. Resting oxygen consumption had a mean coefficient of variation (CV) of 2.4% (range 1-32%). The recovery of oxygen consumption (mVo(2)) after electrical stimulation at 4 Hz was fit to an exponential curve, which represents mitochondrial capacity. The time constant for the recovery of mVo(2) was reproducible with a mean CV of 10% (range 1-22%) only when correcting for blood volume changes. We also examined the effects of adipose tissue thickness on measurements of mVo(2). We found the mVo(2) measurements using absolute units to be influenced by adipose tissue thickness (ATT), and this relationship was removed when an ischemic calibration was performed, supporting its use to compare mVo(2) between individuals of varying ATT. In conclusion, in vivo oxidative capacity can be assessed using blood volume-corrected NIRS signals with a high degree of reliability and reproducibility.

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Cite This Study

Ryan et al. (2012) studied this question.

synapsesocial.com/papers/69daaf1985037e71b2684921https://doi.org/10.1152/japplphysiol.00319.2012
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