Sports Med (2014) 44:1377–1391
DOI 10.1007/s40279-014-0211-9
SYSTEMATIC REVIEW
Heart Rate Variability and Swimming
Julian Koenig • Marc N. Jarczok • Mieke Wasner
Thomas K. Hillecke • Julian F. Thayer
•
Published online: 24 June 2014
Ó Springer International Publishing Switzerland 2014
Abstract
Background and Objectives Professionals in the domain
of swimming have a strong interest in implementing
research methods in evaluating and improving training
methods to maximize athletic performance and competitive
outcome. Heart rate variability (HRV) has gained attention
in research on sport and exercise to assess autonomic
nervous system activity underlying physical activity and
sports performance. Studies on swimming and HRV are
rare. This review aims to summarize the current evidence
on the application of HRV in swimming research and
draws implications for future research.
Methods A systematic search of databases (PubMed via
MEDLINE, PSYNDEX and Embase) according to the
PRISMA statement was employed. Studies were screened
Electronic supplementary material The online version of this
article (doi:10.1007/s40279-014-0211-9) contains supplementary
material, which is available to authorized users.
J. Koenig J. F. Thayer
Department of Psychology, The Ohio State University,
Columbus, OH, USA
J. Koenig (&)
Department of Psychology, Emotions and Quantitative
Psychophysiology Laboratory, The Ohio State University, 175
Psychology Building, 1835 Neil Avenue, Columbus, OH 43210,
USA
e-mail:
[email protected]
M. N. Jarczok
Mannheim Institute of Public Health, Social and Preventive
Medicine, Medical Faculty Mannheim, Heidelberg University,
Mannheim, Germany
M. Wasner T. K. Hillecke
School of Therapeutic Sciences, SRH University Heidelberg,
Heidelberg, Germany
for eligibility on inclusion criteria: (a) empirical investigation (HRV) in humans (non-clinical); (b) related to
swimming; (c) peer-reviewed journal; and (d) English
language.
Results The search revealed 194 studies (duplicates
removed), of which the abstract was screened for eligibility. Fourteen studies meeting the inclusion criteria were
included in the review. Included studies broadly fell into
three classes: (1) control group designs to investigate
between-subject differences (i.e. swimmers vs. non-swimmers, swimmers vs. other athletes); (2) repeated measures
designs on within-subject differences of interventional
studies measuring HRV to address different modalities of
training or recovery; and (3) other studies, on the agreement of HRV with other measures.
Conclusions The feasibility and possibilities of HRV
within this particular field of application are well documented within the existing literature. Future studies,
focusing on translational approaches that transfer current
evidence in general practice (i.e. training of athletes) are
needed.
1 Introduction
Swimming is of the most practiced and most popular forms
of physical activity in the EU [1] and the US [2]. Research
has addressed the beneficial health effects of swimming [3]
(e.g. in the prevention and treatment of cardiovascularrelated diseases [4–7], and in patients with respiratory
impairments such as asthma [8–11]), as well as its psychological (e.g. mood altering) [12–14] and adverse health
effects [15–22].
Besides these fields of research, professionals in the
domain of swimming have a strong interest in
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implementing research methods in evaluating and
improving training methods to maximize athletic performance and competitive outcome. Of particular interest are
methods for the assessment of bio-behavioral (e.g. metabolic and cardioventilatory responses [23]) and endocrinological (e.g. cortisol, testosterone, insulin [24–26])
markers to investigate the effects of swim training and their
relation to performance outcome. Traditionally, research
on exercise physiology utilized a brainless model of human
exercise performance [27], solely focusing on mechanisms
of muscle fatigue. In comparison, contemporary research
emphasizes the central neural networks involved in the
regulation of exercise performance [27]. In particular, the
autonomic nervous system (ANS) has gained huge attention for its vital role in the homeostatic regulation of the
organism to functionally adapt to the demands of the
environment (e.g. exercise and sport) [28, 29].
While the effects of swimming on autonomic outflow
have been studied [30] using blood pressure (BP; e.g. Nualnim et al. [6, 31] and Cox et al. [6, 31]), heart rate (HR;
e.g. Jung and Stolle [32–34], Butler and Woakes [32–34],
and Hauber et al. [32–34]) or similar parameters of cardiovascular activity, HR variability (HRV) in athletes has
only received attention over the last decade [35, 36]. The
characteristic beat-to-beat variation in HR represents the
continuous interplay between the sympathetic and parasympathetic branches of the ANS in regulating HR.
Increases in sympathetic activity are associated with
increases in HR, while relative increases in parasympathetic
activity are associated with decreases in HR. In the resting
condition the heart is under tonic inhibitory control (parasympathetic dominance over sympathetic influences) [37].
Sympathetic effects are slow (on the timescale of seconds),
while parasympathetic effects are faster (on the timescale of
milliseconds [ms]) [38]. Thus, the analysis of changes in the
beat-to-beat variation of the heart is therefore a traceable
proxy measure of the ANS, in particular parasympathetic
vagal activity. Exercise training (in particular endurance
training) is associated with increases in parasympathetic
activity, indexed by greater vagally-mediated HRV [39–
44]. The study of HRV in athletes has been considered a
valuable tool to investigate long-term changes related to
exercise training and ANS activity during exercise [32], as
well as to monitor performance, fitness and freshness [45].
Furthermore, a rationale to study HRV in sport research
is given by findings that emphasize anatomical and functional differences of the cardiovascular system between
competitive athletes and untrained individuals [46]. While
athletes, independent of their sporting activity, have lower
resting HR, recent research on exercise-induced cardiac
remodeling [47] supports the existence of an endurancetrained and a strength-trained heart in athletes performing
dynamic and static sports [48], leading to training-specific
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J. Koenig et al.
changes in cardiac structure and function [49]. Swimming
differs from other popular exercise modalities in many
aspects (i.e. posture, water immersion, upper and lower
body involvement, temperature). The cardiac adaptations
to swim training are characterized by left ventricular
dilatation, normal wall thickness to dimension ratio, and
increased stroke volume with normal diastolic filling [30].
Furthermore, evidence supports differences between longand short-distance swimmers [50]. However, studies on the
effect of swimming on HRV and the usefulness of HRV
methods within the professional application are rare.
Within this systematic review, we attempt to summarize
current findings on the influence of swimming on HRV and
the potential usefulness of HRV as a tool in evaluating
swim training and maximizing performance.
2 Methods
2.1 Search Strategy
This review uses a systematic approach, according to the
Preferred Reporting Items for Systematic Reviews and
Meta-Analyses (PRISMA) statement [51], to synthesize
research on HRV and swimming. The following computerized databases were searched from 1 January 1996 to 31
July 2013: PubMed via MEDLINE, PSYNDEX and Embase (see Electronic Supplementary Material [ESM]
Appendix for search terms and strategies applied, by
database). The search was restricted to publications published within that timeframe, since the first guidelines on
standards of measurements, physiological interpretation
and clinical use of HRV were published in 1996 [52].
Articles were considered for inclusion if they measured
HRV (search term keyword: ‘heart rate variability’ OR
‘HRV’) and (AND) had a focus on swimming or swimmers
(search term keywords: ‘swim*’; see ESM Appendix for
detailed search strategy). Details were recorded regarding
the number of studies found by database and search term,
as depicted within the flowchart (see Fig. 1).
The abstracts of the manuscripts were then independently screened for eligibility by two authors (JK and
MNJ). Differences in initial study identification and
selection for review were compared and deviations were
discussed until consensus on the disposition of each study
under question could be reached. Screening was based on
the following criteria: (a) empirical investigation with
HRV measures taken in humans from non-clinical samples;
(b) specifically related to swimming (i.e. reported training
effects in swimmers); (c) published in a peer-reviewed
journal; and (d) published in English. Included papers were
reviewed in full text for information on (1) study design
and subjects; (2) swimming variables (i.e. elite swimmers,
Heart Rate Variability and Swimming
1379
Fig. 1 Search flow diagram.
HRV heart rate variability
training frequency); (3) method of HRV measurement; (4)
data on HRV time domain measures; and (5) data on frequency domain measures. The few differences in evaluation were addressed, producing the consensus presented in
Fig. 1. The number of studies meeting the pre-specified
inclusion criteria, number of studies excluded, and reasons
for exclusion were recorded.
2.2 Data Extraction
Study information on author, country, study population,
sample size, sex ratio, age of participants, and main study
focus were extracted from the papers retrieved in full text.
Furthermore, details regarding the HRV measures obtained
from data sets were extracted and main findings or reported
effects were derived from the papers retrieved in full text
and summarized within a comprehensive table (Table 1).
Studies were classified and summarized by their study
design (i.e. control group, crossover, other).
3 Results
The search of the selected databases revealed 229 articles
(Fig. 1). A total of 194 articles were considered for
inclusion in the review after removing duplicates. The
abstracts of all articles were retrieved for further screening
of eligibility, leaving 24 articles for further consideration.
These were retrieved in full text if possible. A total of 14
studies [53–66] were finally included in the systematic
review (Fig. 1; Table 1).
3.1 Heart Rate Variability Measures
Besides basic measures of HR (i.e. beats per minute
[BPM]), variations in HR or HRV can be evaluated by
many different methods and measures. Overall, measures
of HRV can be divided into three classes: the time domain,
frequency domain and non-linear. The most commonly
used measures of HRV are summarized in Table 2.
3.1.1 Time Domain Measures
Time domain measures can be derived from direct measurements of the normal-to-normal intervals (NN intervals)
of instantaneous HR, or from the differences between NN
intervals. Within the included studies, reported time
domain measures include the mean NN interval in milliseconds (ms) [53, 61, 65], the mean standard deviation
(SD) of all NN intervals (SDRR or SDNN in ms [54–56,
59, 61, 65, 66]), the square root of the mean of the sum of
the squares of differences between adjacent NN intervals
(RMSSD) in ms [53–56, 59, 63, 65, 66], or the number of
pairs of adjacent NN intervals differing by more than
50 ms divided by the total number of all NN intervals
(pNN50 in % [54–56, 65, 66]) or simple NN50 count [55].
Aside from these frequently used measures, authors
reported the SD of the mean of all NN intervals for 5-min
segments (SDANN [56, 59, 66]) and the mean of the SD of
all normal NN intervals for all 5-min segments (SDNNIDX
[53, 56, 59]). Furthermore, the study by Cervantes Blásquez et al. [55] used the triangular interpolation of NN
interval histogram (TINN), as described elsewhere [62].
3.1.2 Frequency Domains
Parametric and non-parametric methods to analyze the
power spectral density (PSD) of HRV allow the calculation
of different spectral components of short- and long-term
recordings of HRV. From short-term recordings, three
different main spectral components are distinguished: verylow frequency (VLF; B0.04 Hz), low frequency (LF;
usually 0.04–0.15 Hz) and high frequency (HF; usually
0.15–0.4 Hz) components. Furthermore, an ultra-low
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Table 1 Included studies by study design and authors, in alphabetical order
References
Country
Population
HRV measures taken
Main study focus
HRV/swimming related finding
Control group designs
Franke et al.
[58]
USA
Members of the Iowa State University
male intercollegiate swim team (n = 9;
mean age ± SD 20.1 ± 0.4 years) and
track team (n = 11; mean age ± SD
21.3 ± 0.05 years); both groups were
considered to be endurance-trained with
the primary difference in training being
the exercise modality and posture used
HF, LF, LF/HF, TP
To determine whether highly fit swimmers
have greater orthostatic tolerance than
equally fit runners and whether there are
group differences in the autonomic
responses to central hypovolemia
: TP in the runners than the swimmers
throughout LBNP; no significant
differences while SUP and resting; no
significant differences after data
normalization on LF or HF
Lakin et al.
[61]
Canada
Healthy, young subjects (n = 21;
M/F = 11/10a); UT (n = 11; mean
age ± SD 23.0 ± 1 year); TT (n = 10;
mean age ± SD 23.0 ± 1 year); TT:
established triathletes ([2 years of
training and competitive experience), or
recreational triathletes performing a
mixture of running, cycling and swim
training (4–6 days/week, 3–4 h/week per
modality, with exercise sessions,
45–90 min)
HF, LF, LF/HF, NN, SDNN
To compare the effects of intensity- and
duration (30 min)-matched cycling and
swimming (Swim-Cooper-Test) exercise
on the post-exertional (ER, MR, LR)
response in young, healthy TT and UT
individuals
Swimming: UT: ; NN during ER and MR
compared with BL; TT: ; NN, SDNN,
HF and : LF, LF/HF during ER
compared with BL; ; NN, HF and : LF,
LF/HF during MR compared with BL; ;
NN, : LF/HF during ER, MR and LR
compared with cycling; : LF and ; HF
compared with UT
Triposkiadis
et al. [65]
Greece
Highly trained pre-pubertal swimmers
(n = 25; M/F = 15/10; mean age ± SD
11.9 ± 1.6 years) at national and
international level; controls (n = 20;
M/F = 1/6b; mean age ± SD
11.3 ± 0.6 years); training sessions of
12–14 h weekly for at least 4 years
HF, LF, LF/HF, NN,
pNN50, SDNN, RMSSD
To compare HRV in a group of highly
trained pre-pubertal swimmers with
those of active but not training children
: NN, SDNN, pNN50, RMSSD and HF in
swimmers compared with controls; ; LF/
HF in swimmers compared with controls
Vinet et al.
[66]
France
Highly trained pre-pubertal boys,
swimmers (n = 11; mean age ± SD
11.9 ± 0.9 years); age-matched active
controls (n = 9; mean age ± SD
11.6 ± 1.1 years); fitness level
questionnaire (i.e. sport practice, years of
practice, number of hours of sports per
weeks, best record in swimming
competition)
HF, LF, LF/HF, TP,
pNN50, SDNN, RMSSD,
SDANN measures during
sleep
To compare HRV parameters in highly
trained swimmer boys and untrained
counterparts
No statistically significant differences
Highly-trained swimmers (n = 8;
M/F = 4/4; mean age ± SD
19.6 ± 3.2 years); training *21 h per
week; two competed at an international
level, others competed in the first French
National League; all participated in heats
for the national team selection
NN, RMSSD
To investigate the effect of daily CWI
compared with a control condition,
during a typical training week, on
parasympathetic activity and subjective
ratings of well-being
; RMSSD during training week in CON; :
RMSSD during training week in CWI; :
RMSSD in CWI compared with CON on
days 2, 3, 4, 5; : NN in CWI compared
with CON on days 3, 4
Crossover designs
Al Haddad
et al. [53]
France
J. Koenig et al.
References
Population
HRV measures taken
Main study focus
HRV/swimming related finding
Atlaoui et al.
[54]
France
French swimmers competing nationally
and internationally (n = 13); males
(n = 9; mean age ± SD 23 ± 4);
females (n = 4; mean age ± SD
21 ± 2 years); background in
competitive swimming: 15 ± 3 years;
50 m, 100 m, 200 m, 400 m, or 1500 m
specialists (different strokes); trained
6 days per week, usually twice a day,
practiced regular dryland training, 1 h
per day
HF, LF, LF/HF, TP,
pNN50, SDNN, RMSSD,
SDNNIDX
To determine the relationship between
HRV changes and both training
variations (IT, RT) and performances in
elite swimmers
HF correlated with performance during
RT; at the end of RT, performances were
significantly negatively related to LF/HF
and LF and positively related to HF;
between IT and RT periods, changes in
TSF were related to the changes in HF (:
TSF, : HF), LF (: TSF, ; LF) and LF/
HF (: TSF, ; LF/HF)
Cervantes
Blásquez
et al. [55]
Spain
Master swimmers (n = 10; M/F = 4/6;
mean age ± SD 47 ± 6.81 years);
members of the Masters swimming team
of a Spanish private club; mean ± SD
8 ± 2.07 years participating in national
competitions
HF, LF, LF/HF, VLF, NN,
NN50; pNN50, SDNN,
RMSSD, TINN, nonlinear Poincaré analysis
(SD1, SD2)
To examine how the ANS indexed by
HRV regulates the heart during precompetitive anxiety in swimmers under
two different conditions (TC vs. CC)
; RMSSD, HF, SD1 in CC; : LF/HF in
CC
Chalencon
et al. [56]
France
Swimmers of regional to national level
(n = 10), males (n = 6; mean age ± SD
17.3 ± 2.8 years); females (n = 4;
mean age ± SD 15.8 ± 1.9 years);
mean ± SD intensive training history:
5.6 ± 2 years; mean ± SD training
duration 10.7 ± 2.9 h per week during
season
HF, LF, LF/HF, TP,
pNN50, SDNN, RMSSD,
SDANN, SDNNIDX
To compare the response of performance
and nocturnal ANS activity to 31 weeks
of training; to build a model to support a
consistent relationship between ANS
activity, fatigue and sports performance
Significant relationship between HF and
individual performance: : HF = :
performance
Garet et al.
[59]
France
Regional-level swimmers (n = 7;
M/F = 4/3; mean age ± SD
16.6 ± 0.5 years); mean ± SD history
of 6.4 ± 0.9 years of practice
SDNN, RMSSD, SDANN,
SDNNIDX; HFwavelet,
LFwavelet, VLFwavelet,
LFwavelet/HFwavelet,
TPwavelet, measures during
sleep
To quantify the association between
changes in ANS activity and changes in
three 400-m front-crawl swim
performances (Perf1, Perf2, Perf3)
during/at the end of three successive
periods (RP1, TR, RP2) over 7 weeks
; SDNNIDX Perf2 compared with Perf1; :
SDNNIDX Perf3 compared with Perf1;
positive correlation of SDNN,
SDNNIDX, HFwavelet, TPwavelet and
performance
Parouty et al.
[62]
Francec
Well-trained swimmers (n = 10d;
M/F = 5/5; mean age ± SD
19.0 ± 3.9 years) at national level;
24 h week-1 training
RMSSD
The effect of CWI compared with CON on
sprint swimming performance
CWI was associated with a ‘likely’ smaller
decrease in RMSSD, with a standardized
difference considered as ‘moderate’
Perini et al.
[63]
Italy
Swimmers (n = 9; M/F = 3/6; mean
age ± SD 15.9 ± 1.55 years); involved
in swimming activity at competitive
level for at least 5 years
HF, LF, LF/HF, TP for SUP
and ST position
To test if seasonal training is associated
with changes of HRV before and at the
end of the competitive season
None of the calculated parameters of HRV
were significantly affected by training,
no significant HRV differences at postseason compared with pre-season
Schmitt et al.
[64]
France
National-level male swimmers (n = 8;
mean age ± SD 17.0 ± 1.8 years); no
further specification
HF, LF, LF/HF, TP for SUP
and ST position
To test the hypothesis that training
(17 days, twice a day) at two different
altitudes (1200 m vs. 1850 m) induces
specific modifications of HRV
: TPSUP, TPST, HFSUP, LFST during
1200 m altitude; change in performance
between altitudes was correlated with the
change in HFSUP
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Country
Heart Rate Variability and Swimming
Table 1 continued
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Table 1 continued
References
Country
Population
HRV measures taken
Main study focus
HRV/swimming related finding
Di Michele
et al. [57]
Italy
High-level swimmers (n = 14); males
(n = 6; mean age ± SD 19.6 ± 3.0);
females (n = 8; mean age ± SD
15.5 ± 6.0 years); all athletes competed
at the national or international level, and
most were specialized in the front-crawl
style; mean ± SD training experience:
male: 8.2 ± 2.6 years, female:
5.4 ± 2.3 years
HFPOW: HFPOW-RSA,
HFPOW-STR
To assess the agreement between HRV
and LA to estimate the AT in an
incremental front-crawl swimming test
Overall, very good agreement between LA
and HRV to estimate AT
Hellard et al.
[60]
France
Elite swimmers (n = 18; M/F = 10/8;
age: 19–30e years)
HF, LF, LF/HF, VLF, nonlinear Poincaré analysis
(SD1, SD2) for SUP and
OP
To test the hypothesis that a shift in
autonomic balance toward sympathetic
predominance is associated with a higher
risk of infection in swimmers
: Parasympathetic indexes assessed
1 week earlier in SUP linked to : risk of
URTPI and MP; same week: risk of MP
in SUP linked with : in sympathetic and
parasympathetic and gain in LF/HF;
same week: ; HF associated with : risk
of MP; : AP risk in winter and for an :
TP associated with a decline in SD1 in
SUP; OP in winter: ; HF week earlier :
risk of AP; gain in LF/HF linked to an
increase in URTPI and MP; : LF and ;
SD1 in OP associated with an : risk of
MP
Other studies
Classes of studies: (1) control group design; (2) repeated measures design; (3) other design
ANS autonomic nervous system, AP all-type pathologies, AT anaerobic threshold, BL baseline, CC competition condition, CON out-of-water control condition, CWI cold-water immersion, ER
early recovery, F female subjects, HF high-frequency HRV, HFPOW high-frequency spectral power, HFPOW-RSA high-frequency power relative to respiratory sinus arrhythmia, HFPOW-STR highfrequency spectral power relative to the stroking modulation of heart rate, HRV heart rate variability, IT intense training, LA blood lactate concentration, LBNP lower body negative pressure,
LF/HF low-frequency high-frequency ratio, LF low-frequency HRV, LR late recovery, M male subjects, MP muscular problems, referred to as muscle injury, pulled muscles, tendinopathies,
delayed-onset muscle soreness persisting [24 h after training, shoulder-pain syndrome, and knee-pain syndrome, MR mid recovery, NN normal-to-normal intervals, NN50 count of adjacent
cycles greater than 50 ms apart, OP orthostatic position, Perf x performance number, pNN50 percentage of adjacent cycles greater than 50 ms apart, RMSSD square root of the mean of the sum
of the squared differences between adjacent normal RR intervals, RP1 recovery period 1, RP2 recovery period 2, RT reduced training, SD standard deviation, SD1 instantaneous beat-to-beat
variability, SD2 long-term beat-to-beat variability, SDANN standard deviations of the mean of all normal RR intervals, SDNN standard deviation of all normal RR intervals, SDNNIDX mean of
the standard deviation of all normal RR intervals for all 5-min segments, ST standing, SUP supine position, TC training condition, TINN triangular interpolation of NN intervals, TP total power,
TR training period, TSF total score of fatigue, TT triathlon trained, URTPI upper respiratory tract and pulmonary infections, UT untrained, VLF very-low frequency HRV, x wavelet frequency
domain measures determined by wavelet transform analysis, : indicates an increase of the selected measure, ; indicates a decrease of the selected measure
a
No sex ratio per group is reported
b
The reported sex ratio by the authors probably relates to a writing error and should be 14/6
Unclear where participants were recruited; country was derived from the affiliation of the first author
c
Due to a technical failure with the HR belt in two participants, HR measures were only available in eight subjects
e
No mean age is reported
J. Koenig et al.
d
Name
Description/definition
Unit
HR
Simple heart rate
BPM
IBI
Raw duration of R-wave to R-wave intervals
ms
ANS branch
Mixed
Heart Rate Variability and Swimming
Table 2 Frequently used HRV measures
Time domain measures (based on the interbeat intervals directly or on differences between successive interbeat intervals. In addition, there are both short- and long-term indices)
NN
Normal-to-normal intervals
ms
Mixed
SDNN
SDANN
Standard deviation of all NN intervals
Standard deviation of the average of NN intervals for each 5-min period over 24 h
ms
ms
Mixed
Mixed
pNN50
Percentage of adjacent cycles that are greater than 50 ms apart
%
Primarily vagally mediated
RMSSD
Root mean square of successive differences. This index acts like a high-pass filter, thus removing long-term trends and slower- ms
Primarily vagally mediated
frequency variability from the signal. Because of the frequency characteristics of the autonomic influences on the heart, such
that vagal influences cover the full frequency range and sympathetic influences are primarily restricted to the lower frequencies,
RMSSD reflects primarily vagal influences
Frequency domain measures (frequency domain analysis yields information about the amount of variance or power in the heart rate or heart period time series explained by periodic oscillations
at various frequencies. Power spectral analysis of the time series provides basic information on the amount of variance or power as a function of frequency)
HF
High frequency (0.15–0.4 Hz)
ms2
Primarily vagally mediated
LF
Low frequency (0.04–0.15 Hz)
ms2
Baroreflex activity
VLF
Very-low frequency (0.003–0.04 Hz)
ms2
Mixed
ULF
Ultra-low frequency (\0.003 Hz)
ms2
Mixed
TP
Total power represents the variance of the measured signal about its mean value exactly equal to the time domain variance of the
HR time series
ms2
Mixed
Normalization
The so-called normalized scores represent the relative value of each power component in portion to the total power. In addition,
the VLF or DC component is often subtracted from the total power in calculating the normalized values. The DC component is
defined as the spectral components with a frequency less than 0.03 Hz
–
Mixed
LF/HF
The LF to HF ratio (LF/HF) has been proposed to reflect the sympathovagal balance. The LF to HF ratio may provide some insight
into the relative relationship among autonomic influences
–
Baroreflex activity
HRV heart rate variability, ANS autonomic nervous system, BPM beats per minute, DC mean value of the waveform
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frequency component (ULF) can be derived from spectral
analysis in long-term recordings (e.g. 24 h). Depending on
the length of the recording, different frequency domain
measures with different frequency bands (see Table 1) are
reported within the included studies, including the power in
HF [54–58, 60, 61, 63–66], the power in LF [54–56, 58, 60,
61, 63–66], the power in VLF [55, 60], or total power (TP)
[54, 56, 58, 63, 64, 66]. Additionally, the ratio between LF
and HF (LF/HF ratio) serves as another measure of HRV
and is frequently included within the reviewed studies [54–
56, 58, 60, 61, 63–66]. Respiratory sinus arrhythmia
(RSA), the square root of the mean squared difference of
successive NNs (RMSSD) and the high-frequency component of the power spectrum (HFPOW) are closely related
and are strongly associated with cardiac vagal influence
and thus represent parasympathetic activity (Table 2). On
the other hand, and contrary to conventional wisdom, lowfrequency HRV (LF) reflects baroreflex activity rather than
sympathetic activity [67–69].
Besides these frequently used measures (Table 2), one
study [57] reported a different method to analyze the HF
component. The authors separated the HFPOW (spectral
power in the HF range [0.15–2 Hz]) of each spectrum into
two components. The first component included the spectral
power relative to the respiratory modulation of HR
(HFPOW-RSA), whereas the second component included the
spectral power relative to the stroking (locomotor) modulation of HR (HFPOW-STR). Details on this approach are
described elsewhere [57]. Furthermore, one study [59]
reported wavelet-transformed frequency domain measures
of HFwavelet, LFwavelet, VLFwavelet, LFwavelet/HFwavelet, and
TPwavelet. In case of HRV analysis, the wavelet transform
analysis is devoted to the extraction of characteristic frequencies, contained along a signal of consecutive NN
intervals. The analysis amounts to sliding a window of
different weights (corresponding to different levels) containing the wavelet function, all along the signal, as further
described by the authors [59].
3.1.3 Non-Linear Measures
Two of the included studies [55, 60] used non-linear Poincaré analysis to calculate indices of HRV. The Poincaré
method consists of plotting the length of each NN interval
against the length of the previous NN interval. Both studies
[55, 60] used two standard Poincaré plot descriptors: the
SD1 is a measure of instantaneous variability (successive
beats) and is taken as an indicator of parasympathetic
activity, whereas the SD2 represents long-term variability
and indicates both parasympathetic and sympathetic
activities.
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3.2 Nature of Included Studies
The included studies broadly fell into three classes: (1) studies
using a control group design to compare HRV in swimmers
with subjects allocated to a control group (e.g. non-swimmers,
runners); (2) interventional studies measuring HRV over
training progress (e.g. relating HRV to performance measures
in swimmers), measuring HRV to address different modalities
of training (e.g. differences in altitude, intense vs. reduced
training) or recovery (i.e. cold-water immersion [CWI])
within a repeated measures design; and (3) other studies using
HRV to address a specific problem (e.g. association of HRV
and risk of infection in swimmers, pre-competitive anxiety in
swimmers, HRV to estimate anaerobic threshold (AT)—
mostly correlation studies).
3.2.1 Control Group Designs: Differences
in the Autonomic Nervous System Function
Three studies investigated differences in ANS function
indexed by HRV in swimmers compared with a control
group (control group design). Of these, two studies investigated differences in HRV in highly trained pre-pubertal
swimmers compared with untrained counterparts. The
earlier study by Triposkiadis et al. [65] found a predominance of vagal tone in prepubertal swimmers. All parameters of HRV that are strongly dependent on
parasympathetic activity—both in the time domain and the
frequency domain measures (Table 2)—were significantly
increased in prepubertal swimmers compared with controls
(Table 1). The later study by Vinet et al. [66] reported no
significant differences between groups (swimmers vs.
untrained boys) for all frequency domain measures independent of the mode of expression (absolute in ms2, relative in ln or %) and time domain measures. The authors
mentioned that their results demonstrated that participating
intensively in swimming training does not induce changes
in HRV indices. Regarding the controversial nature of their
results compared with Triposkiadis et al. [65], Vinet et al.
[66] argue that differences between the two studies could
be explained by the population studied (boys and girls vs.
boys; training volume: 12–14 h per week vs. 8–10 h per
week) and different methods of quantifying HRV.
The study by Franke et al. [58] also focused on differences in ANS function by determining whether highly fit
swimmers have greater orthostatic tolerance in comparison
to equally fit runners, and whether there are group differences in the autonomic responses to central hypovolemia.
However, the authors summarized that neither orthostatic
tolerance nor HRV responses to graded lower body negative pressure (LBNP) within a testing chamber differed
between the runners and swimmers, suggesting that
Heart Rate Variability and Swimming
differences between run and swim training do not affect
these responses.
Lakin et al. [61] compared the effects of intensity- and
duration-matched cycling and swimming exercise on the
post-exertional early-, mid- and late-recovery response in
young, healthy, triathlon trained (TT) and untrained (UT)
individuals. In the UT group, there were no significant
differences in indices of ANS function between the cycling
and swimming exercise group. However, the TT group
demonstrated a significant increase in LF and decrease in
HF at early- and mid-recovery compared with pre-exercise
following swimming, and increase in the LF/HF compared
with baseline and cycling exercise after swimming, indicating a slower recovery of these indices following
swimming [61]. No differences between the groups were
observed following cycling exercise. Following swimming,
significant group differences during early- and mid-recovery were present. The authors suggested that HRV response
to exercise is dependent on both training status and exercise modality [61].
Of these higher class (i.e. better-designed, controlled)
studies, two showed significant differences between the
groups studied, while two other studies did not reveal any
difference in ANS function or reactivity, as indexed by
HRV, between groups. One study revealed a predominance
of vagal tone in highly trained pre-pubertal swimmers
compared with untrained counterparts [65], while a later
study with a similar research question and design [66]
failed to replicate these findings. One study [61] found
differences in the post-exertional recovery response in triathlon-trained subjects compared with untrained individuals after swimming, while another study [58] was not able
to report differences in highly fit swimmers compared with
equally fit runners in the autonomic responses to central
hypovolemia.
3.2.2 Crossover Designs: Variations in Training, Task
or Recovery Modalities
The majority of studies used a repeated measures design
for the evaluation of variations within the experimental
protocol and their comparative effects on HRV. These
variations addressed different training intensities (intense
training vs. reduced training, Atlaoui et al. [55]), different
conditions (training condition vs. competition condition,
Cervantes Blásquez et al. [55]; intensive training vs. taper
recovery periods, Chalencon et al. [56]; resting period vs.
training period, Garet et al. [59]), different times of the
season (before vs. at the end of the competitive season,
Perini et al. [63]), different training locations (altitude:
1,200 vs. 1,850 m, Schmitt et al. [64]), or different
recovery modalities (CWI, Al Haddad et al. [53, 63] and
Perini et al. [53, 63]).
1385
Three studies [54, 56, 59] showed that HR was significantly related to swimming performance. In particular,
greater HF power—representing parasympathetic activity—was significantly associated with greater performance
[54]. However, one study [59] assessed measurements of
HRV and autonomic function while participants were
asleep, which is not comparable with the other two studies
[54, 56].
The study by Atlaoui et al. [54] measured HRV in
competing national and international swimmers over a
7-week period. The swimmers were tested before and after
a 4-week intense training period (IT) and a 3-week reduced
training period (RT). At the end of each period, the
swimmers performed in a competition and answered a
questionnaire on fatigue. The authors found that HF HRV
correlated with performance both during and at the end of
RT, i.e. performances were significantly negatively related
to LF HRV and LF/HF ratio, and positively related to HF.
Furthermore, the authors found changes in fatigue positively related to changes in HF and negatively related to LF
and LF/HF ratio between the IT and RT periods. The
authors summarized their findings that HF, LF and LF/HF
are significantly related to swimming performance, and
those swimmers with higher HF and lower LF/HF, after the
3 weeks of RT, reported lower fatigue [54]. However, no
significant changes in HRV with training load variations
were found. The authors concluded that in highly trained
swimmers who coped well with their training program,
higher levels of HF during taper constituted a favorable
condition to increased swimming performance, and that
HRV changes during that time are a valuable tool for
monitoring the adaptation in variations of training load
and, hence, to improve performance in elite swimmers
during periods of reduced training.
Garet et al. [59] aimed to quantify the association
between changes in night-time ANS activity and changes
in three 400-m front-crawl swim performances during or at
the end of three successive periods of recovery or training
over 7 weeks. The training load of the swimmers was
reduced between the intensive training period (following a
first recovery period) and the recovery periods. While no
differences in mean performance between the three
assessments were found, mean SDNNIDX showed a quadratic trend, such that there was a decrease in performance
from 1 to 2, and a rise back to baseline in performance 3.
The authors reported various trends for wavelet transform
indices of TP and HF—that are associated with global and
parasympathetic activity—and wavelet transform indices
of LF, but did not report on the significance of effects [59].
However, when individual data was plotted against associated changes in performance, TP (TPwavelet) showed a
significant positive correlation. Furthermore, other correlations with time (i.e. SDNNIDX) and frequency measures
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associated with global and parasympathetic activity were
significant but weaker. The authors concluded that individual relative variations in performance and individual
relative variations in nocturnal ANS activity are closely
related [59].
Chalencon et al. [56] observed swimmers of regional to
national level over 31 weeks at two cycles of intensive
training and taper recovery periods to compare the
response of performance in weekly morning 400-m freestyle time trials and nocturnal ANS activity. The authors
found a logarithmic relationship between performance and
ANS activity, where higher HF was associated with greater
performance. The authors concluded that their results
demonstrated the relevance of HRV measurement as a
valuable tool to assess physiological training-induced
responses and to optimize athletic performance [56].
Cervantes Blásquez et al. [55] addressed differences of
pre-competitive anxiety and HRV in swimmers under a
training condition (TC) and a competition condition (CC),
and found HRV related to pre-competitive anxiety under
different conditions. Pre-competitive anxiety scores for
somatic anxiety on the Competitive State Anxiety
Inventory-2 (CSAI-2) were higher in the CC than the TC.
The authors noticed a significant decrease in the RMSSD,
whereas all other time domain measures of HRV showed
no significant differences between the conditions. Nonlinear HRV analysis revealed that SD1 was significantly
lower during CC. Furthermore, there was a significant
increase of the LF/HF ratio and a decrease of HF in the
CC. All parameters that increased their value significantly
in the CC were related to sympathetic activity and all
parameters that decreased significantly were related to
parasympathetic activity. Overall, the authors provided
evidence for a change in autonomic control in competitive
situations and in the presence of pre-competitive anxiety
[55].
Another study [63] showed that improvement in physical fitness observed from the beginning to the end of the
athletes’ competitive season was associated with decreased
HR and BP at rest, but with no change in the corresponding
vagal and sympathetic spectral markers indexed by HRV.
The authors found significant differences on various HRV
measures in the supine and sitting position, but no significant HRV differences at post-season compared with the
pre-season were observed. The authors concluded that the
improvement in physical fitness observed from the beginning to the end of the athletes’ competitive season was
associated with decreased HR and BP values at rest, but
with no change in the corresponding vagal and sympathetic
spectral markers indexed by HRV [63].
Significant effects of the altitude of the training location
on HRV were revealed in another study [52]. During
training at an altitude of 1200 m, various HRV indices
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J. Koenig et al.
increased. However, none of these parameters changed
during training at an altitude of 1,850 m; nevertheless,
swimming performance improved. Again, and this deserves
special notice, the authors found the change in performance
was correlated with an increase in vagal activity, as
indexed by HF HRV. The authors tested the hypothesis that
17 days of training (twice a day) at two different altitudes
(1,200 vs. 1,850 m) induces specific modifications of HRV.
They observed a difference in HRV changes between the
two altitudes. During training at an altitude of 1,200 m,
supine and standing TP and supine HF, as well as standing
LF, were increased. Furthermore, the 2,000-m freestyle
performance was improved, whereas none of these
parameters changed during training at an altitude of
1,850 m. Most interestingly, the change in performance
was correlated with an increase in supine HF. The authors
noted that HRV analysis in altitude appears to be a
promising method for monitoring the interacting effects of
hypoxia and training loads as high training loads and
hypoxic stress may have cumulative effects on HRV by
decreasing spectral power [64]. Their results are in line
with the study by Chalencon et al. [56] who found a logarithmic relationship between performance and ANS
activity, where higher HF was associated with greater
performance. Based on the evidence from these studies,
one may generally conclude that greater HRV, especially
HF, is associated with better swim performance.
Furthermore, two studies investigated the effect of CWI
[62] or daily CWI [53] as recovery intervention for
swimmers. While one study found that the intervention
resulted in slower swimming times and a smaller decrease
in RMSSD [62], the other study [53] found that daily
intervention following training was associated with greater
resting cardiac parasympathetic activity indexed by
RMSSD. Parouty et al. [62] investigated the effect of CWI
compared with an out-of-water control condition on sprint
swimming performance in well-trained swimmers who
were randomly assigned to a specified sequence of conditions. Each participant completed both conditions on two
testing sessions at the same time of day, 6–7 days apart.
CWI was associated with a decrease in swimming performance and a smaller decrease in RMSSD after the first of
two 100-m swimming sprints. The authors concluded that,
despite a subjective perception of improved recovery following CWI, the intervention resulted in slower swimming
times and therefore is unlikely to provide any performance
benefit to well-trained swimmers [62]. In a similar study
design, Al Haddad et al. [53] investigated the effect of
daily CWI compared with a control condition where subjects rested seated without immersion, during a typical
training week, on parasympathetic activity and subjective
ratings of well-being in a randomized crossover design.
The authors found that daily CWI recovery following
Heart Rate Variability and Swimming
training was associated with greater resting cardiac parasympathetic activity—indexed by RMSSD—and a better
maintenance of perceived sleep quality throughout the
training week. As direct benefits of CWI on physical performance and training adaptation warrants further investigations, the authors concluded that future studies
investigating the influence of other immersion modalities
on subjective ratings, ANS activity, training adaptation and
performance are needed [53].
3.2.3 Other Studies
Two other studies with different study designs to those
described above were included in the systematic review. Di
Michele et al. [57] assessed the relationship between HRV
and lactate concentration (LA) to estimate the AT in an
incremental front-crawl swimming test in high-level
swimmers. The authors found an overall strong relationship
between LA and HRV to estimate AT. They concluded that
it is possible to estimate the AT from the HRV in an
incremental front-crawl swimming test and that the strong
agreement between the HRV threshold and the LAAT
supports the possibility of using the HRV-based method for
the actual testing of swimmers [57].
Hellard et al. [60] tested the hypothesis that a shift in
autonomic balance toward sympathetic predominance is
associated with a higher risk of infection in swimmers.
They observed 18 elite swimmers over the time course of
2 years in two Olympic preparation centers. Symptoms and
HRV were measured on a weekly basis, with eight HRV
variables quantified in the supine and orthostatic positions.
The authors found that an increase in parasympathetic
indexes in the supine position assessed 1 week earlier was
linked to a higher risk of upper respiratory tract and pulmonary infections (URTPI) and muscular problems (MP;
muscle injury, pulled muscles, tendinopathies, delayedonset muscle soreness persisting [24 h after training,
shoulder-pain syndrome, and knee-pain syndrome) [60].
During the same week of measurement and symptom
documentation, a higher risk of MP was linked with an
increase in sympathetic and parasympathetic indices and a
gain in the LF/HF. Measured in the orthostatic position, a
decrease in HF was associated with an increased risk of MP
measured during the same week, and a gain in the LF/HF
ratio was statistically linked to an increase in URTPI and
MP. Furthermore, increased LF and decreased SD1 in the
OR position were associated with an increased risk of MP,
and an increase in the TP of HRV associated with a decline
in SD1 in the supine position was associated with a higher
risk for all-type pathologies in winter. The authors summarized their findings and noted that the weeks that preceded the appearance of URTPI and MP were
characterized by an increase in autonomic parasympathetic
1387
activity in the supine position. Therefore, the authors
concluded that HRV is a rapid and non-invasive tool to
indicate autonomic function, which provides complementary information that may help to reduce the risk of
infection in elite swimmers [60].
4 Discussion
The present systematic review aimed to summarize trends
in the use of HRV measurements in the field of swimming
research. A search of three prominent electronic databases
by defined search strategies (see ESM Appendix), according to the PRISMA statement, revealed 194 total studies
(after removing duplicates). Abstracts were then screened
for eligibility for inclusion within the review under predefined inclusion criteria. An extensive search strategy of
three major databases was applied. However, the review is
still limited as one full text was not retrieved and several
conference proceedings were not included. Fourteen studies meeting the inclusion criteria were included within the
review. Besides one study from the US and one from
Canada, all studies were conducted in Europe, with studies
coming from France (n = 8), Italy (n = 2), Greece
(n = 1), and Spain (n = 1). All included studies were
published after the year 2000, with nine studies published
between 2000 and 2012, and six studies published within
the last 3 years. The first guideline [52] on standards of
measurements, physiological interpretation and clinical use
of HRV was published in 1996 and, thus, only studies
published after 1996 were included in the review. Included
studies therefore show a general good reporting of HRV
methods applied and measures derived. Most studies
reported the frequently used measures of HRV that are
summarized in Table 2. However, differences in the
methods of HRV recording carry a potential bias when
comparing results from different laboratories that use different devices to record HRV or different algorithms for its
analysis. Furthermore, measuring HRV during swimming,
or shortly after exercise, comes with several methodological challenges. Most studies used ambulatory devices such
as the s810 [53, 54, 56, 59, 60, 62, 63], or the S810i [55,
57] (Polar Electro, Kempele, Finland). Although these
Polar recorders have been reported as reliable and valid
tools when compared with an ECG [70, 71], and are more
practical in such applied situations due to the affordability
of the device [72], if possible, traditional ECGs should be
used for both gathering and editing of HRV data [73].
Furthermore, as thermoregulation is driven by the ANS,
HRV measurements are affected by changes in the environmental temperature [74, 75] that might occur by transition of athletes wearing only swim clothes into or out of
the water. While some authors’ demonstrated possible
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ways to control for core and skin temperature [61] in study
designs that required HRV assessment shortly after or
during exercise, the general influence of environmental
factors in this particular field of research appears to have
been underestimated.
Studies reviewed in this article fell mainly into three
classes; control group designs [58, 61, 65, 66] to investigate between-subject differences (i.e. swimmers vs. nonswimmers, swimmers vs. other athletes); repeated measures designs [53–56, 59, 62–64] on within-subject differences of interventional studies measuring HRV to address
different modalities of training or recovery; and other
studies not falling into one of the aforementioned classes of
studies—using HRV to address a specific problem such as
the association of HRV and risk of infection in swimmers.
The controversial results from control group designs on
differences in the ANS function between trained and
untrained subjects [65 vs. 66, 58 vs. 61] are probably driven by methodological aspects that are crucial and should
always be taken into account when interpreting and comparing HRV data from different studies. For example, the
studies by Triposkiadis et al. [65] and Vinet et al. [66] not
only differed in sample size (n = 25/20 vs. n = 11/9) and
sex ratio (boys and girls vs. boys) but also on length of
HRV recording (512 RR intervals vs. 6 min of a total of
4 h of recordings), the condition of recording (at rest vs.
during sleep) and the technical device used (12-lead ECG
vs. portable holter monitoring). Differences in the studies
by Franke et al. [58] and Lakin et al. [61] might also result
from different sample sizes (n = 9/11 vs. 21/10), sex ratios
(only male vs. balanced), length of HRV recording (256
RR intervals vs. 5 min), the condition of recording (supine
vs. seated position), and the technical device used (5-lead
vs. 3-lead ECG). While some of these results are therefore
controversial, they reveal that investigating HRV differences between (1) trained and untrained individuals or (2)
different types of athletes, and by (3) task and/or (4)
training modality are fields of interest for future studies.
Crossover designs with repeated measures foremost
focused on the improvement of training modalities for
professional swimmers. From this class of included studies
one can generally state that HRV seems to be related to
swimming performance. Of particular interest for future
studies is the investigation of (1) the specific role of
parasympathetic activity indexed by time (i.e. RMSSD,
pNN50) and frequency domain measures (i.e. HF) of
HRV—as most studies revealed a significant correlation of
performance measures with these parameters of HRV; (2)
the effect of recovery interventions on the ANS that can be
assessed using measures of HRV; and (3) to explore to
what extent HRV can mirror the impact of different
training modalities. The particular association of swim
training and vagal activity is in line with findings from
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J. Koenig et al.
research on animals. Recent research in rats suggests that
resting bradycardia (induced by swim training) is mainly
mediated by parasympathetic activity and differs from
other training modes (i.e. running) that seem to decrease
intrinsic HR [76]. Future studies in humans should
emphasize this particular association and investigate the
differences between swimming and other modalities of
physical activity. However, since numerous factors influence autonomic modulation of the HR (e.g. age, time of the
day, nutrition) and thus affect experimental data, caution should be used in implying causation in the results of
studies, which are largely based on correlation data. Prospective trials and well-controlled replication studies are
necessary to strengthen the existing evidence on a possible
relation between HRV and swimming performance.
Besides the studies summarized with control group and
crossover designs, two other studies were included in the
systematic review. One [57] assessed the agreement
between HRV and LA to estimate the AT in swimmers and
found that it is possible to estimate the AT from the HRV.
Recently, several studies aimed to develop methods for
estimating the AT [77] from HRV [78, 79]. HRV allows
the differentiation of sub- from supra-ventilatory-threshold
exercise [79], and oxygen consumption at the ventilation
AT level was related to the variance of RR intervals [78].
However, given the large variability in both measures, the
feasibility of such applications needs to be questioned. It
has been shown that combined methods are superior (over
the use of a single method) and more accurate in the
determination of ventilatory thresholds. Based on the evidence reviewed, this should also be taken into account
when using HRV to determine ventilatory threshold. The
other study [60] found that changes in HRV are associated
with the risk of infection in swimmers, and provides
information that may help to reduce the risk of infection in
elite swimmers. These types of studies promote the integration of the use of HRV measures in regular training in
professional athletes, and the latter study points to the
prospective value of HRV assessment. While clinical
research emphasizes the prognostic or predictive value of
HRV [80–84], the study by Hellard et al. [60] was the only
one treating HRV as independent variable to predict the
risk of infection. The utility of HRV to determine individual training load or expected performance outcome by a
priori baseline assessment might further be of interest in
the development of new fields of research.
5 Conclusion
The assessment of ANS activity underlying physical
activity is of interest for professionals in the field of sports
to improve training processes and competitive outcomes.
Heart Rate Variability and Swimming
Of particular interest seems the appropriate assessment of
parasympathetic activity, as recent research suggests that a
high and relatively stable vagal activity during preparation
may indicate a readiness to train or appropriate recovery
that positively affects performance in athletes [85]. Furthermore, measures of training-induced disturbances
in autonomic control may provide useful information for
training prescription [86]. HRV provides a feasible, noninvasive measurement for the quantification of ANS
activity and allows the distinct evaluation of vagal activity
by different time and frequency domain measures
(Table 2). Therefore, HRV has several advantages compared with other measures of cardiovascular activity during
exercise.
However, studies on cardiac variability in athletes are
still an almost unexplored domain [35]. While recommendations for the standardization of measurement conditions in future studies on athletes that also apply for
swimmers are given elsewhere [35], this review provides
a summary of the current evidence from HRV research on
swimming and recommendations for future directions.
Besides studies that focus on the outcome and effects of
frequent swimming on ANS function, especially in adolescents, the majority of studies included in this review
used measures of HRV to mirror and improve training or
competition conditions and performance outcome in professional athletes. With respect to these studies, the
review revealed two major findings: (1) performance in
professional swimmers is correlated with ANS activity indexed by HRV (particularly parasympathetic activity); and (2) differences in training and recovery
modalities can be illustrated by methods of HRV measurement and analysis.
While the feasibility and possibilities of HRV measures
for this particular field of application are well documented
within the existing literature, it seems that their incorporation in regular everyday training is far from realized
because HRV research on swimming faces several methodological challenges related to the particular nature of the
sporting activity. Existing studies encourage the use of
HRV measures for a broad variety of applications by
trainers, athletes and experts within the field but more
research is needed, focusing on translational approaches
that transfer current evidence into regular practice.
Acknowledgments Julian Koenig, Marc Jarczok, Mieke Wasner,
Thomas Hillecke and Julian Thayer declared no potential conflicts of
interest with respect to the research, authorship and/or publication of
this article. The work on the present manuscript was not funded by
any source. None of the authors was involved in any of the articles
included in the systematic review. We like to thank all the authors
who provided us with the full text of their studies. We thank DeWayne P. Williams for proof reading the manuscript and language
corrections. Furthermore, we thank the three anonymous reviewers
for their valuable comments on our manuscript.
1389
References
1. Vaz de Almeida MD, Graca P, Afonso C, et al. Physical activity
levels and body weight in a nationally representative sample in
the European Union. Public Health Nutr. 1999;2:105–13.
2. US Census Bureau. The 2009 statistical abstract of the United
States. Washington, DC: Department of Commerce; 2009.
3. Chase NL, Sui X, Blair SN. Swimming and all-cause mortality
risk compared with running, walking, and sedentary habits in
men. Int J Aquat Res Educ. 2008;2:213–23.
4. World Hypertension League. Physical exercise in the management of hypertension: a consensus statement by the World
Hypertension League. J Hypertens. 1991;9:283–7.
5. Tanaka H, Bassett DR Jr, Howley ET, et al. Swimming training
lowers the resting blood pressure in individuals with hypertension. J Hypertens. 1997;15:651–7.
6. Nualnim N, Parkhurst K, Dhindsa M, et al. Effects of swimming
training on blood pressure and vascular function in adults
[50 years of age. Am J Cardiol. 2012;109:1005–10.
7. Tanaka H. Swimming exercise: impact of aquatic exercise on
cardiovascular health. Sports Med. 2009;39:377–87.
8. Huang SW, Veiga R, Sila U, et al. The effect of swimming in
asthmatic children: participants in a swimming program in the
city of Baltimore. J Asthma. 1989;26(2):117–21.
9. Rosimini C. Benefits of swim training for children and adolescents with asthma. J Am Acad Nurse Pract. 2003;15:247–52.
10. Beggs S, Foong YC, Le HC, et al. Swimming training for asthma
in children and adolescents aged 18 years and under. Cochrane
Database Syst Rev. 2013;4:CD009607. doi:10.1002/14651858.
CD009607.pub2.
11. Weisgerber MC, Guill M, Weisgerber JM, et al. Benefits of
swimming in asthma: effect of a session of swimming lessons on
symptoms and PFTs with review of the literature. J Asthma.
2003;40:453–64.
12. Berger BG, Owen DR. Mood alteration with swimming: swimmers really do ‘‘feel better’’. Psychosom Med. 1983;45:425–33.
13. Berger BG, Owen DR. Mood alteration with yoga and swimming:
aerobic exercise may not be necessary. Percept Mot Skills.
1992;75:1331–43.
14. Valentine E, Evans C. The effects of solo singing, choral singing
and swimming on mood and physiological indices. Br J Med
Psychol. 2001;74:115–20.
15. Kaydos-Daniels SC, Beach MJ, Shwe T, et al. Health effects
associated with indoor swimming pools: a suspected toxic chloramine exposure. Publ Health. 2008;122:195–200.
16. Schoefer Y, Zutavern A, Brockow I, et al. LISA study group.
Health risks of early swimming pool attendance. Int J Hyg
Environ Health. 2008;211:367–73.
17. Pilotto LS, Douglas RM, Burch MD, et al. Health effects of
exposure to cyanobacteria (blue-green algae) during recreational
water-related activities. Aust N Z J Public Health. 1997;21:
562–6.
18. Momas I, Brette F, Spinasse A, et al. Health effects of attending a
public swimming pool: follow up of a cohort of pupils in Paris.
J Epidemiol Community Health. 1993;47:464–8.
19. Agabiti N, Ancona C, Forastiere F, et al. Short term respiratory
effects of acute exposure to chlorine due to a swimming pool
accident. Occup Environ Med. 2001;58:399–404.
20. Bougault V, Boulet LP. Airway dysfunction in swimmers. Br J
Sports Med. 2012;46:402–6.
21. Uyan ZS, Carraro S, Piacentini G, et al. Swimming pool, respiratory health, and childhood asthma: should we change our
beliefs? Pediatr Pulmonol. 2009;44:31–7.
22. Bernard A, Nickmilder M, Voisin C. Outdoor swimming pools
and the risks of asthma and allergies during adolescence. Eur
Respir J. 2008;32:979–88.
123
1390
23. Lavin KM, Guenette JA, Smoliga JM, et al. Controlled-frequency
breath swimming improves swimming performance and running
economy. Scand J Med Sci Sports. Epub 24 Oct 2013. doi:10.
1111/sms.12140.
24. Tyndall GL, Kobe RW, Houmard JA. Cortisol, testosterone, and
insulin action during intense swimming training in humans. Eur J
Appl Physiol Occup Physiol. 1996;73:61–5.
25. Bonifazi M, Bela E, Carli G, et al. Responses of atrial natriuretic
peptide and other fluid regulating hormones to long distance
swimming in the sea. Eur J Appl Physiol Occup Physiol.
1994;68:504–7.
26. Huttunen P, Lando NG, Meshtsheryakov VA, et al. Effects of
long-distance swimming in cold water on temperature, blood
pressure and stress hormones in winter swimmers. J Therm Biol.
2000;25:171–4.
27. Okano AH, Fontes EB, Montenegro RA, et al. Brain stimulation
modulates the autonomic nervous system, rating of perceived
exertion and performance during maximal exercise. Br J Sports
Med. 2013. doi:10.1136/bjsports-2012-091658.
28. Caterini R, Delhomme G, Dittmar A, et al. A model of sporting
performance constructed from autonomic nervous system
responses. Eur J Appl Physiol Occup Physiol. 1993;67:250–5.
29. Fu Q, Levine BD. Exercise and the autonomic nervous system.
Handb Clin Neurol. 2013;117:147–60.
30. Lazar JM, Khanna N, Chesler R, et al. Swimming and the heart.
Int J Cardiol. 2013;168:19–26.
31. Cox KL, Burke V, Beilin LJ, et al. Blood pressure rise with swimming versus walking in older women: the Sedentary Women Exercise Adherence Trial 2 (SWEAT 2). J Hypertens. 2006;24:307–14.
32. Jung K, Stolle W. Behavior of heart rate and incidence of
arrhythmia in swimming and diving. Biotelem Patient Monit.
1981;8:228–39.
33. Butler PJ, Woakes AJ. Heart rate in humans during underwater
swimming with and without breath-hold. Respir Physiol.
1987;69:387–99.
34. Hauber C, Sharp RL, Franke WD. Heart rate response to submaximal and maximal workloads during running and swimming.
Int J Sports Med. 1997;18:347–53.
35. Aubert AE, Seps B, Beckers F. Heart rate variability in athletes.
Sports Med. 2003;33:889–919.
36. Petry D, Marques JLB. System for heart rate variability analysis
in athletes. IFMBE Proc. 2013;33:311–4.
37. Jose AD, Collison D. The normal range and determinants of the
intrinsic heart rate in man. Cardiovasc Res. 1970;4:160–7.
38. Levy MN. Neural control of cardiac function. Baillieres Clin
Neurol. 1997;6:227–4.
39. Melanson EL, Freedson PS. The effect of endurance training on
resting heart rate variability in sedentary adult males. Eur J Appl
Physiol. 2001;85:442–9.
40. Madden KM, Levy WC, Stratton JK. Exercise training and heart
rate variability in older adult female subjects. Clin Invest Med.
2006;29:20–8.
41. Jurca R, Church TS, Morss GM, et al. Eight weeks of moderateintensity exercise training increases heart rate variability in sedentary postmenopausal women. Am Heart J. 2004;147:e21.
42. Catai AM, Chacon-Mikahil MP, Martinelli FS, et al. Effects of
aerobic exercise training on heart rate variability during wakefulness and sleep and cardiorespiratory responses of young and
middle-aged healthy men. Braz J Med Biol Res. 2002;35:741–52.
43. Howorka K, Pumprla J, Haber P, et al. Effects of physical training
on heart rate variability in diabetic patients with various degrees
of cardiovascular autonomic neuropathy. Cardiovasc Res.
1997;34:206–14.
44. Davy KP, Willis WL, Seals DR. Influence of exercise training on
heart rate variability in post-menopausal women with elevated
arterial blood pressure. Clin Physiol. 1997;17:31–40.
123
J. Koenig et al.
45. Plews DJ, Laursen PB, Stanley J, et al. Training adaptation and
heart rate variability in elite endurance athletes: opening the door
to effective monitoring. Sports Med. 2013;43:773–81.
46. Fagard RH. Impact of different sports and training on cardiac
structure and function. Cardiol Clin. 1997;15:397–412.
47. Weiner RB, Baggish AL. Exercise-induced cardiac remodeling.
Prog Cardiovasc Dis. 2012;54:380–6.
48. Pluim BM, Zwinderman AH, van der Laarse A, et al. The athlete’s heart: a meta-analysis of cardiac structure and function.
Circulation. 2000;101:336–44.
49. Baggish AL, Wang F, Weiner RB, et al. Training-specific
changes in cardiac structure and function: a prospective and
longitudinal assessment of competitive athletes. J Appl Physiol.
2008;104:1121–8.
50. D’Andrea A, Caso P, Sarubbi B, et al. Right ventricular myocardial adaptation to different training protocols in top-level
athletes. Echocardiography. 2003;20(4):329–36.
51. Moher D, Liberati A, Tetzlaff J, The PRISMA Group, et al.
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339:b2535.
52. Task Force of the European Society of Cardiology and the North
American Society of Pacing and Electrophysiology. Heart rate
variability: standards of measurement, physiological interpretation, and clinical use. Eur Heart J. 1996;17:354–81.
53. Al Haddad H, Parouty J, Buchheit M. Effect of daily cold water
immersion on heart rate variability and subjective ratings of wellbeing in highly trained swimmers. Int J Sports Physiol Perform.
2012;7:33–8.
54. Atlaoui D, Pichot V, Lacoste L, et al. Heart rate variability,
training variation and performance in elite swimmers. Int J Sports
Med. 2007;28:394–400.
55. Cervantes Blásquez JC, Rodas Font G, Capdevila Ortı́s L. Heartrate variability and precompetitive anxiety in swimmers. Psicothema. 2009;21:531–6.
56. Chalencon S, Busso T, Lacour JR, et al. A model for the training
effects in swimming demonstrates a strong relationship between
parasympathetic activity, performance and index of fatigue. PLoS
One. 2012;7:e52636.
57. Di Michele R, Gatta G, Leo AD, et al. Estimation of the anaerobic threshold from heart rate variability in an incremental
swimming test. J Strength Cond Res. 2012;26:3059–66.
58. Franke WD, Mills KK, Lee K, et al. Training mode does not
affect orthostatic tolerance in chronically exercising subjects. Eur
J Appl Physiol. 2003;89:263–70.
59. Garet M, Tournaire N, Roche F, et al. Individual interdependence
between nocturnal ANS activity and performance in swimmers.
Med Sci Sports Exerc. 2004;36:2112–8.
60. Hellard P, Guimaraes F, Avalos M, et al. Modeling the association between HR variability and illness in elite swimmers. Med
Sci Sports Exerc. 2011;43:1063–70.
61. Lakin RA, Notarius C, Thomas SG, et al. Effects of moderateintensity aerobic cycling and swim exercise on post-exertional
blood pressure in healthy, young untrained and triathlon-trained
men and women. Clin Sci. 2013;125:543–53.
62. Parouty J, Al Haddad H, Quod M, et al. Effect of cold water
immersion on 100-m sprint performance in well-trained swimmers. Eur J Appl Physiol. 2010;109:483–90.
63. Perini R, Tironi A, Cautero M, et al. Seasonal training and heart
rate and blood pressure variabilities in young swimmers. Eur J
Appl Physiol. 2006;97:395–403.
64. Schmitt L, Hellard P, Millet GP, et al. Heart rate variability and
performance at two different altitudes in well-trained swimmers.
Int J Sports Med. 2006;27:226–31.
65. Triposkiadis F, Ghiokas S, Skoularigis I, et al. Cardiac adaptation
to intensive training in prepubertal swimmers. Eur J Clin Invest.
2002;32:16–23.
Heart Rate Variability and Swimming
66. Vinet A, Beck L, Nottin S, et al. Effect of intensive training on
heart rate variability in prepubertal swimmers. Eur J Clin Invest.
2005;35:610–4.
67. Casadei B, Cochrane S, Johnston J, et al. Pitfalls in the interpretation of spectral analysis of the heart rate variability during
exercise in humans. Acta Physiol Scand. 1995;153:125–31.
68. Moak JP, Goldstein DS, Eldadah BA, et al. Supine low-frequency
power of heart rate variability reflects baroreflex function, not
cardiac sympathetic innervation. Cleve Clin J Med. 2009;76:
S51–9.
69. Goldstein DS, Bentho O, Park MY, et al. Low-frequency power
of heart rate variability is not a measure of cardiac sympathetic
tone but may be a measure of modulation of cardiac autonomic
outflows by baroreflexes. Exp Physiol. 2011;96:1255–61.
70. Loimaala A, Sievänen H, Laukkanen R, et al. Accuracy of a
novel real-time microprocessor QRS detector for heart rate variability assessment. Clin Physiol. 1999;19:84–8.
71. Weippert M, Kumar M, Kreuzfeld S, et al. Comparison of three
mobile devices for measuring R-R intervals and heart rate variability: Polar S810i, Suunto t6 and an ambulatory ECG system.
Eur J Appl Physiol. 2010;109:779–86.
72. Parrado E, Garcı́a MA, Ramos J, et al. Comparison of Omega
Wave System and Polar S810i to detect R-R intervals at rest. Int J
Sports Med. 2010;31:336–41.
73. Wallén MB, Hasson D, Theorell T, et al. Possibilities and limitations of the Polar RS800 in measuring heart rate variability at
rest. Eur J Appl Physiol. 2012;112:1153–65.
74. Fleisher LA, Frank SM, Sessler DI, et al. Thermoregulation and
heart rate variability. Clin Sci. 1996;90:97–103.
75. Okamoto-Mizuno K, Tsuzuki K, Mizuno K, et al. Effects of low
ambient temperature on heart rate variability during sleep in
humans. Eur J Appl Physiol. 2009;105:191–7.
76. Medeiros A, Oliveira EM, Gianolla R, et al. Swimming training
increases cardiac vagal activity and induces cardiac hypertrophy
in rats. Braz J Med Biol Res. 2004;37:1909–17.
1391
77. Svedahl K, MacIntosh BR. Anaerobic threshold: the concept and
methods of measurement. Can J Appl Physiol. 2003;28:299–23.
78. Seluyanov VN, Kalinin EM, Pack GD, et al. Estimation of the
anaerobic threshold from the data on lung ventilation and heart
rate variability. Human Physiol. 2011;37:733–7.
79. Cottin F, Médigue C, Leprêtre PM, et al. Heart rate variability
during exercise performed below and above ventilatory threshold.
Med Sci Sports Exerc. 2004;36:594–600.
80. Nicolini P, Ciulla MM, De Asmundis C, et al. The prognostic
value of heart rate variability in the elderly, changing the perspective: from sympathovagal balance to chaos theory. Pacing
Clin Electrophysiol. 2012;35:622–38.
81. Nolan J, Batin PD, Andrews R, et al. Prospective study of heart
rate variability and mortality in chronic heart failure: results of
the United Kingdom heart failure evaluation and assessment of
risk trial (UK-heart). Circulation. 1998;98:1510–6.
82. Ong MEH, Padmanabhan P, Chan YH, et al. An observational,
prospective study exploring the use of heart rate variability as a
predictor of clinical outcomes in pre-hospital ambulance patients.
Resuscitation. 2008;78:289–97.
83. Boveda S, Galinier M, Pathak A, et al. Prognostic value of heart
rate variability in time domain analysis in congestive heart failure. J Interv Card Electrophysiol. 2001;5:181–7.
84. Galinier M, Pathak A, Fourcade J, et al. Depressed low frequency
power of heart rate variability as an independent predictor of
sudden death in chronic heart failure. Eur Heart J. 2000;21:
475–82.
85. Botek M, McKune AJ, Krejci J, et al. Change in performance in
response to training load adjustment based on autonomic activity.
Int J Sports Med. 2014;35:482–8.
86. Borresen J, Lambert MI. Autonomic control of heart rate during
and after exercise: measurements and implications for monitoring
training status. Sports Med. 2008;38:633–46.
123