Evaluation of nocturnal heart rate variability for strenuous exercise day using wearable photoelectric pulse wave sensor

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J Exerc Rehabil Vol. 14, No. 4, 633-637, August, 2018

Publication date (electronic) : 2018 August 24

doi : https://doi.org/10.12965/jer.1836321.156

Yutaka Yoshida^1,, Emi Yuda², Kiyoko Yokoyama¹, Junichiro Hayano²

¹Nagoya City University Graduate School of Design and Architecture, Nagoya, Japan

²Department of Medical Education, Nagoya City University Graduate School of Medical Science, Nagoya, Japan

^*Corresponding author: Yutaka Yoshida, https://orcid.org/0000-0001-5676-3048, Nagoya City University Graduate School of Design and Architecture, 2-1-10, Kita Chikusa, Chikusa-ku, Nagoya 464-0083, Japan, Tel: +81-52-721-5439, Fax: +81-52-721-3110, E-mail: yoshida@sda.nagoya-cu.ac.jp

Received 2018 June 24; Accepted 2018 July 24.

Abstract

INTRODUCTION

Physical activity has been reported to control cardiovascular risk factors such as obesity, diabetes mellitus, hypertension, and so on (Dhutia and Sharma, 2015). During the leisure time, the mortality rate of people with high physical activity is lower than the mortality rate of people with low physical activity (Arem et al., 2015; Liu et al., 2018). According to World Health Statistics 2016, Japan’s healthy life expectancy is the world’s No. 1 (83.7 years), and relationship between health life expectancy (World Health Organization, 2016) and heart rate variability (HRV) has also been reported from Japanese Holter electrocardiogram big data (Yuda et al., 2017). HRV reflects autonomic nervous activity, and decline of HRV is recognized as cardiovascular risk and mortality risk (Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology, 1996).

Exercise reduces HRV, but changes nocturnal HRV are affected by exercise habits, exercise intensity, time zones. In the previous study, walking and jogging for healthy young during 30 min in the morning did not have a significant influence nocturnal HRV (Yuda et al., 2018). Other studies have reported that moderate exercise and marathon in the afternoon (Myllymäki et al., 2012), and strong exercise in the evening from 6:00 p.m. increase nocturnal heart rate (HR) and lower nocturnal HRV (Hynynen et al., 2010). Generally, although exercise is a beneficial activity, overworking can stress the body and sometimes reduce nocturnal HRV (Driver and Taylor, 2000). Therefore, monitoring the recovery of nocturnal HRV leads to the determination of an appropriate exercise protocol.

In this study, we examined whether or not the strenuous exercise in the evening change nocturnal HRV and recovers. Nocturnal HRV on holiday exercise day and weekday working day was analyzed using wearable photoelectric pulse wave sensor for amateur futsal team in their 30s.

MATERIALS AND METHODS

Measurements

Before the game started, the activity meter (Lifecorder GS, Suzuken Co., Ltd., Nagoya, Japan) was worn on the waist and the energy expenditure (EE) (kcal) of the physical activity during the game was measured. Using the wearable photoelectric pulse wave sensor, pulse waves during sleeping was measured at home on exercise day and on Wednesday (control day) of after 3 days too. Washout of exercise effect was 3 days. Also, the EE of control day was measured from wake-up time to bedtime, and refrained from drinking alcohol on both exercise day and control day.

Wearable photoelectric pulse wave sensor

Pulse wave and body movement acceleration during sleep were measured using the wearable photoelectric pulse wave sensor with built-in 3-axis acceleration sensor (APM, prototype, Suzuken Co. Ltd., Nagoya, Japan). External dimensions are W52×D46×H21 mm, mass is 46 g, pulse wave is detected with LED (peak emission wavelength 570 nm) and photodetector. Piezoresistive type was used for 3-axis acceleration sensor (dynamic range, ±3 G). Sampling frequency is 32 Hz, pulse wave can be continuously recorded for 12 hr by the lithium ion battery.

Analysis of pulse wave and 3-axis acceleration

After applying complex demodulation (CDM) to the pulse wave signal (Hayano et al., 1994), pulse interval time series was calculated at 2 Hz using pulse interval demodulation which directly extracts the instantaneous pulse interval as a continuous function from the pulse wave signal (Hayano et al., 2005). Fig. 1 shows pulse interval time series, pulse wave signal and 3-axis acceleration during night sleep. The mean pulse interval (MPI) and standard deviation pulse interval (SDPI) were calculated from the pulse interval time series. In addition, as frequency analysis, amplitude of the low frequency component (LF, 0.04–0.15 Hz) corresponding to HRV, amplitude of the high frequency component (HF, 0.15–0.45 Hz) and the ratio of LF to HF (LF/HF) were calculated using CDM. All indices were calculated as calculation window for 30 min. Bedtime was defined as the time when the change of 3-axis acceleration disappeared. Wake-up time was defined as the time which the acceleration change occurred when subjects woke up.

Fig. 1

Calculation of pulse interval time series using pulse interval demodulation and 3-axis acceleration. Measurement time is 0:35 a.m.−6:35 a.m., bed time is 1:00 a.m., wake-up time is 6:30 a.m. Upper panel: pulse interval time series. Middle panel: original pulse wave time series. Lower panel: 3-axis acceleration.

RESULTS

Fig. 2 shows change of HRV indices during night sleep (mean± standard error). MPI, SDPI, LF, HF of exercise day were significantly lower than those of control day (P<0.0001). LF/HF of exercise day was significantly higher than that of control day (P< 0.05). Regarding change of HRV for sleep phase, MPI (P<0.05), SDPI (P=0.0003), LF (P=0.0038), HF (P<0.05) were observed significant changes. No interaction was observed between condition and sleep phase in all indices. EE during exercise was 247± 88 kcal, EE on control day was 207±76 kcal.

Fig. 2

Change of heart rate variability indices during sleep calculated using complex demodulation. Subjects were 8 healthy men. Sleeping time of exercise day was 362±43 min, Sleeping time of control day was 347±70 min (mean±standard deviation). MPI, mean pulse intervals; SDPI, pulse intervals of standard division; LF, low-frequency component amplitude; HF, high-frequency component amplitude; LF/HF, LF-to-HF component power ratio.

DISCUSSION

In this study, to examine whether or not the strenuous exercise in the evening changes nocturnal HRV and recovers, we compared exercise day with control day. MPI, SDPI, LF, and HF of exercise day were significantly lower than control day. These gentle increases were observed for 120 min after going to bed, after that, variability was suppressed, MPI and HF did not reach the level of control day. HF of HRV reflects cardiac parasympathetic activity, and LF/HF reflects cardiac sympathetic nerve activity. Since HF decreases and LF/HF increases as compared to the control day, it is thought that strenuous exercise in the evening promotes sympathetic nervous activity during night sleep and suggesting that pulse rate and HRV have not recovered by the wake-up time.

As limitations of experiments, we did not measure maximum oxygen intake in this experiment, but instead we measured the amount of physical activity during exercise and control day using activity meter. The experimental protocol of this study carried out an intermittent exercise load of about 90 min repeated 6 times for 7-min futsal and 7-min break. The actual movement time was about 42 min, and the amount of physical activity at this time was 247±88 kcal. The result of recovery delay with increase of HR and decrease of HRV during night sleep for strenuous exercise in the evening are consistent with the study results of Myllymaki et al. (2012).

According to a report of Myllymaki et al. (2012), as a result of exercise from 6:00 p.m. in experimental protocols of exercise intensity (maximum oxygen intake, 45%, 60%, 75%) and exercise time (30 min, 60 min, 90 min) for healthy men in their 30s, nocturnal HR increased with exercise intensity than control day and nocturnal HRV was lower after the 90 min exercise day compared to control day. Hynynen et al. (2010) reported that nocturnal HR was increased and nocturnal HRV was lower than control day in an experiment that combined a moderate exercise of 50 min in the afternoon and a marathon of 3.5 hr.

Although these previous studies are results using electrocardiogram measurement, our study is the result of using a wrist watch type wearable photoelectric pulse wave sensor which can be measured conveniently in daily life. This suggests the possibility of self-monitoring autonomic nervous activity by using wearable photoelectric pulse wave sensor in daily life and it is an important research material for popularization of wearable photoelectric pulse wave sensor. Strenuous exercise in the evening for healthy men in their 30s, nocturnal pulse rate, reduces nocturnal HRV, and did not recover by the wake-up time.

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