Monitoring Changes in Oxygen Muscle during Exercise with High-Flow Nasal Cannula Using Wearable NIRS Biosensors

Exercise increases the cost of breathing (COB) due to increased lung ventilation ([Formula: see text] E), inducing respiratory muscles deoxygenation ([Formula: see text] SmO(2)), while the increase in workload implies [Formula: see text] SmO(2) in locomotor muscles. This phenomenon has been proposed as a leading cause of exercise intolerance, especially in clinical contexts. The use of high-flow nasal cannula (HFNC) during exercise routines in rehabilitation programs has gained significant interest because it is proposed as a therapeutic intervention for reducing symptoms associated with exercise intolerance, such as fatigue and dyspnea, assuming that HFNC could reduce exercise-induced [Formula: see text] SmO(2). SmO(2) can be detected using optical wearable devices provided by near-infrared spectroscopy (NIRS) technology, which measures the changes in the amount of oxygen bound to chromophores (e.g., hemoglobin, myoglobin, cytochrome oxidase) at the target tissue level. We tested in a study with a cross-over design whether the muscular desaturation of m.vastus lateralis and m.intercostales during a high-intensity constant-load exercise can be reduced when it was supported with HFNC in non-physically active adults. Eighteen participants (nine women; age: 22 ± 2 years, weight: 65.1 ± 11.2 kg, height: 173.0 ± 5.8 cm, BMI: 21.6 ± 2.8 kg·m(−2)) were evaluated in a cycle ergometer (15 min, 70% maximum watts achieved in ergospirometry ([Formula: see text] O(2)-peak)) breathing spontaneously (control, CTRL) or with HFNC support (HFNC; 50 L·min(−1), fiO(2): 21%, 30 °C), separated by seven days in randomized order. Two-way ANOVA tests analyzed the [Formula: see text] SmO(2) (m.intercostales and m.vastus lateralis), and changes in [Formula: see text] E and [Formula: see text] SmO(2)· [Formula: see text] E(−1). Dyspnea, leg fatigue, and effort level (RPE) were compared between trials by the Wilcoxon matched-paired signed rank test. We found that the interaction of factors (trial × exercise-time) was significant in [Formula: see text] SmO(2)-m.intercostales, [Formula: see text] E, and ([Formula: see text] SmO(2)-m.intercostales)/ [Formula: see text] E (p < 0.05, all) but not in [Formula: see text] SmO(2)-m.vastus lateralis. [Formula: see text] SmO(2)-m.intercostales was more pronounced in CTRL during exercise since 5′ (p < 0.05). Hyperventilation was higher in CTRL since 10′ (p < 0.05). The [Formula: see text] SmO(2)· [Formula: see text] E(−1) decreased during exercise, being lowest in CTRL since 5′. Lower dyspnea was reported in HFNC, with no differences in leg fatigue and RPE. We concluded that wearable optical biosensors documented the beneficial effect of HFNC in COB due to lower respiratory [Formula: see text] SmO(2) induced by exercise. We suggest incorporating NIRS devices in rehabilitation programs to monitor physiological changes that can support the clinical impact of the therapeutic intervention implemented.