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.2023 Dec 1;325(6):R797-R808.
doi: 10.1152/ajpregu.00148.2023. Epub 2023 Oct 23.

Acute nasal breathing lowers diastolic blood pressure and increases parasympathetic contributions to heart rate variability in young adults

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Acute nasal breathing lowers diastolic blood pressure and increases parasympathetic contributions to heart rate variability in young adults

Joseph C Watso et al. Am J Physiol Regul Integr Comp Physiol..

Abstract

There is growing interest in how breathing pace, pattern, and training (e.g., device-guided or -resisted breathing) affect cardiovascular health. It is unknown whether the route of breathing (nasal vs. oral) affects prognostic cardiovascular variables. Because nasal breathing can improve other physiological variables (e.g., airway dilation), we hypothesized that nasal compared with oral breathing would acutely lower blood pressure (BP) and improve heart rate variability (HRV) metrics. We tested 20 adults in this study [13 females/7 males; age: 18(1) years, median (IQR); body mass index: 23 ± 2 kg·m-2, means ± SD]. We compared variables between nasal- and oral-only breathing (random order, five min each) using paired, two-tailedt tests or Wilcoxon signed-rank paired tests with significance set toP < 0.05. We report the median (interquartile range) for diastolic BP and means ± SD for all other variables. We found that nasal breathing was associated with a lower mean BP (nasal: 84 ± 7 vs. oral: 86 ± 5 mmHg,P = 0.006, Cohen'sd = 0.70) and diastolic BP [nasal: 68(8) vs. oral: 72(5) mmHg,P < 0.001, Rank-biserial correlation = 0.89] but not systolic BP (nasal: 116 ± 11 vs. oral: 117 ± 9 mmHg,P = 0.48, Cohen'sd = 0.16) or heart rate (HR; nasal: 74 ± 10 vs. oral: 75 ± 8 beats·min-1,P = 0.90, Cohen'sd = 0.03). We also found that nasal breathing was associated with a higher high-frequency (HF) contribution to HRV (nasal: 59 ± 19 vs. oral: 52 ± 21%,P = 0.04, Cohen'sd = 0.50) and a lower low frequency-to-HF ratio at rest (nasal: 0.9 ± 0.8 vs. oral: 1.2 ± 0.9,P = 0.04, Cohen'sd = 0.49). These data suggest that nasal compared with oral breathing acutely1) lowers mean and diastolic BP,2) does not affect systolic BP or heart rate, and3) increases parasympathetic contributions to HRV.NEW & NOTEWORTHY There is growing interest in how breathing pace, pattern, and training (e.g., device-guided or -resisted breathing) affect prognostic cardiovascular variables. However, the potential effects of the breathing route on prognostic cardiovascular variables are unclear. These data suggest that nasal compared with oral breathing1) lowers mean and diastolic blood pressure (BP),2) does not affect systolic BP or heart rate (HR), and3) increases parasympathetic contributions to heart rate variability (HRV). These data suggest that acute nasal breathing improves several prognostic cardiovascular variables.

Keywords: blood pressure; blood pressure variability; breathing; cardiac vagal baroreflex; heart rate variability.

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Conflict of interest statement

No conflicts of interest, financial or otherwise, are declared by the authors.

Figures

None
Graphical abstract
Figure 1.
Figure 1.
Experimental design. Participants visited the laboratory on one occasion for consent, screening, and testing. The experimental protocol included three 5-min periods at rest with free breathing (to measure participants’ self-selected breathing rate) before nasal-only and oral-only breathing in random order. Next, participants completed the same paradigm (free breathing then randomized nasal and oral breathing) during three 7-min periods while cycling at 75 W on a lower-body ergometer.
Figure 2.
Figure 2.
Brachial blood pressure during rest.A: systolic blood pressure (BP) was not different between conditions. Mean (B) and diastolic (C) BP were lower during nasal breathing. We used two-tailed, pairedt tests for all tests except diastolic BP (Wilcoxon test).n = 20 for all graphs.
Figure 3.
Figure 3.
Heart rate variability metrics during rest. Heart rate (A), the standard deviation of NN intervals (SDNN,B), the percentage of detected NN intervals greater than 50 ms different from the immediately preceding NN interval (pNN50,C), and the low-frequency (LF) contribution were not different between conditions (D). The high-frequency (HF) contribution was lower (E) and the low-frequency (LF)/HF ratio (F) was higher during nasal breathing. We used two-tailed, pairedt tests for all tests except SDNN (Wilcoxon test).n = 20 for all graphs.
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