ArticlePDF Available

High Training Volumes are Associated with a Low Number of Self-Reported Sick Days in Elite Endurance Athletes

Authors:

Abstract and Figures

It has been proposed that high exercise loads increase the risk of infection, most frequently reported as upper respiratory tract infections, by suppressing the immune system. Most athletes will not train when experiencing sickness due to the fear of health complications. However, high training volumes are incompatible with high rates of non-training days, regardless of the cause. The purpose of this observational study was to examine the relationship between self-reported, exercise-constraining days of sickness (days when the athlete decided not to train due to symptoms of disease, either self-reported or by a physician) and the volumes of exercise training in elite endurance athletes by analyzing data from training logs kept for several years. The subjects included 11 elite endurance athletes (8 male, 3 female) competing at national and international levels in cross-country skiing, biathlon and long-distance running. Training logs available from these 11 subjects added to a total of 61 training years. The number of training hours per year (462, 79-856; median, range) was significantly and negatively correlated to the reported number of days not training due to sickness (15, 0-164) by a 3(rd) degree polynomial regression (R(2) = 0.48, F ratio = 18, p < 0.0001). We conclude that elite endurance athletes can achieve high training volumes only if they also experience few sick-days. Key pointsTop level performance demands high training volumes and intensities, which may compromise immune function.Elite athletes must have an immune system capable of intact function also when under sever physiological and psychological stress.Elite performance, especially in endurance sports, is therefore incompatible with a high rate of infections.A negative correlation between infections and exercise training load among elite athletes is consequently observed - the less sick you are the more you can train.
Content may be subject to copyright.
©Journal of Sports Science and Medicine (2014) 13, 929-933
http://www.jssm.org
Received: 25 June 2014 / Accepted: 02 September 2014 / Published (online): 01 December 2014
High Training Volumes are Associated with a Low Number of Self-Reported
Sick Days in Elite Endurance Athletes
Sandra Mårtensson, Kristina Nordebo and Christer Malm
Sports Medicine Unit and School of Sports Sciences, Umeå University, Sweden
Abstract
It has been proposed that high exercise loads increase the risk of
infection, most frequently reported as upper respiratory tract
infections, by suppressing the immune system. Most athletes
will not train when experiencing sickness due to the fear of
health complications. However, high training volumes are in-
compatible with high rates of non-training days, regardless of
the cause. The purpose of this observational study was to exam-
ine the relationship between self-reported, exercise-constraining
days of sickness (days when the athlete decided not to train due
to symptoms of disease, either self-reported or by a physician)
and the volumes of exercise training in elite endurance athletes
by analyzing data from training logs kept for several years. The
subjects included 11 elite endurance athletes (8 male, 3 female)
competing at national and international levels in cross-country
skiing, biathlon and long-distance running. Training logs availa-
ble from these 11 subjects added to a total of 61 training years.
The number of training hours per year (462, 79-856; median,
range) was significantly and negatively correlated to the report-
ed number of days not training due to sickness (15, 0-164) by a
3rd degree polynomial regression (R2 = 0.48, F ratio = 18, p <
0.0001). We conclude that elite endurance athletes can achieve
high training volumes only if they also experience few sick-
days.
Key words: Upper respiratory tract symptoms, infection, high
volume training, immunosuppression.
Introduction
High training intensities and volumes increase the risk of
infection by impairing the immune function (Nieman,
2003; Nieman et al., 1989; 1990; Pedersen and Ullum,
1994; Peters and Bateman, 1983). Thus, elite athletes with
high training intensities have a higher number of infec-
tious episodes than recreational athletes and sedentary
people (Gleeson and Walsh, 2012; Spence et al., 2007).
However, in order to become an elite athlete absence of
infections are important, and such findings may appear
illogical (Malm, 2006). One issue in earlier studies has
been that some conclusions regarding elite exercise train-
ing are based on non-elite athletes (Heath et al., 1991;
Nieman et al., 1989; 1990) or on comparing athletes to
non-athletes (Nieman et al., 2000). In addition, few stud-
ies have confirmed that pathogenic infections are present,
but such studies have made statements that elite exercise
training increases the odds ratio for an infection (Spence
et al., 2007). Most athletes do not have the facilities re-
quired to carry out on-demand virus titers or establish
bacterial cultures, and thus refrain from training based
exclusively on self-diagnosis. The experience of these
athletes thus makes the term Exercise Constrained Sick
Days more appropriate. This can be defined as any day
when the athlete chose not to train due to experienced
symptoms of infections, self-reported or by a physician.
The relationship between the long term risk of
URTI, immune function and exercise load is commonly
modelled as a J-shaped curve with URTI on the y-axis
and exercise load on the x-axis (Nieman, 1994a). This
model suggests that sedentary individuals have a fixed
risk of URTI, and that moderate exercise training de-
creases, while intense exercise training increases, the rate
of URTI by a mechanism in which the immune system is
modulated. Recently, support for this model was present-
ed (Spence et al., 2007). The acute, repeated occurrence
of impairment of immunity, the “open window” for in-
fections to enter the body (Brines et al., 1996; Nieman,
1997; Pedersen and Bruunsgaard, 1995; Pedersen and
Ullum, 1994) may result in a long-term increase in infec-
tion rates (the J-shaped curve).
We have previously shown that infection rates af-
ter a marathon increased only in subjects who had report-
ed a pre-race infection (Ekblom et al., 2006). Consequent-
ly, we formed the hypothesis that the relationship between
training and infection may form an S-curve when true
elite athletes are included (Malm, 2006). Most studies
have not differentiated between athletes with “high” and
“elite” exercise loads, with the consequence that an incor-
rect definition of “elite” athletes has been used. We pre-
sented a pilot study data from one elite runner’s training
log that covered 16 years (Malm, 2006), and concluded
that an increased rate of infection is incompatible with a
high training volume. These findings are in line with the
recently published review article by Dhabhar (Dhabhar,
2014), where short term physical stress such as exercise,
which is perceived as a positive event by the athlete, be-
longs to the immunoprotective response, enhancing sur-
vival and promoting enhanced physical performance.
The aim of this study was to test the hypothesis
that exercise training loads are negatively correlated to the
self-reported number of Exercise Constrained Sick Days.
Methods
Subjects
Male (N = 4) and female (N = 3) cross-country (XC)
skiers, male biathletes (N = 2) and male long-distance
runners (N = 2) completed the study. The inclusion crite-
rion was that the athlete should have demonstrated “top
national or international level performance in an endur-
ance sports”. This does introduce a certain amount of
Research article
Infections in elite athletes
930
subjectivity into whether the criterion was met, but all
subjects were accepted as elite athletes to the School of
Sports Science at Umeå University based on their compet-
itive results from past years. Subjects were aged 17-24
years at the first year of reporting, and they reported a
training period of 3-16 years. The number of observations
of training years was 61 in all statistical calculations. A
retrospective Power calculation was done (using the soft-
ware G*power, version 3.1.3, www.psycho.uni-
duesseldorf.de/abteilungen/aap/gpower3/) for Chi2 tests
(goodness-of-fit for contingency tables) using an effect
size of 0.3, p = 0.05, N = 61 and 2 degrees of freedom
(between three levels of training volume) results in a
Power of 0.54, while increasing the effect size to 0.5
gives a power of 0.95. Ethical permission (Ref. No. 2011-
236-31M) was granted by the Regional Ethics Committee
for northern Sweden, located at Umeå University. All
subjects signed an informed consent form and the study
was conducted in accordance with the WMA Declaration
of Helsinki Ethical Principles for Medical Research
Involving Human Subjects 2008. The study met also the
ethical standards of IJSM (Harriss and Atkinson, 2011).
Procedure
Endurance athletes, who often keep rigorous records of
their training, were asked to summarize their written
training logbooks. Training volume (km or hours), the
number of sick days and the number of days injured had
to have been recorded for participation. Eleven endurance
athletes’ training logs from the past 3-16 years (pending
number of complete years recorded) met these criteria,
and were summarized. Training logs are based on a daily
subjective recordings, thus the definitions of “sick” and
“injured” do not necessarily include examination by a
physician, but always resulted in a no-training day. Con-
sequently, the term self-reported Exercise Constrained
Sick Days is used. Raw data from the training logs were
summarized by the researchers in 12 month intervals as
the sum of hours or kilometres of training, number of
Exercise Constrained Sick Days due to sickness, and
number of days injured (defined as trauma or over-use
injuries) each year. Four subjects did not report the num-
ber of days injured in their training logs, without stating a
reason for not reporting. A minimum of three years of
reported training was required for inclusion. Two athletes
(runners) summarized training in kilometres, which were
transformed into training hours using an assumed average
speed of 4 min 20 sec·km-1, for an elite distance runner or
cross country skier, in which distance-training, interval-
training and recovery running are averaged. Other varia-
bles, such as modes of training, diet, sleeping habits,
travel schedules, medication, hygienic habits or other
potential confounding factors were not taken into consid-
eration. Dietary records and performance variables were
not included. Subjects participated in the elite athletic
program at the School of Sports Science, Umeå Universi-
ty, demanding at least a top national performance level.
The authors have no conflicts of interest.
Statistical analysis
All statistical calculations were carried out in JMP 7.0.1
(SAS Institute Inc. Cary, NC, USA). We investigated
correlations using third-degree polynomial regression
fitting. The Exercise Constrained Sick Days data was not
normally distributed, and thus the data was log-
transformed before partition analysis. The 11 athletes had
trained for a total of 61 years, with a span of 3-16 years.
In order to investigate the correlation between training
volume and the number of Exercise Constrained Sick
Days, these 61 years were divided into three groups based
on the number of Exercise Constrained Sick Days report-
ed, using partition statistics (JMP 7.0.1). Partition was
made to give 3 groups for which the differences between
the groups was most significant (lowest p-value) when
comparing number of training hours. We analysed the
difference in number of training hours between the three
groups using the non-parametric Kruskal-Wallis test. No
adjustment for age was made. Due to the low number of
subjects in each sport, and each sex, no further division of
data, such as split between sports or sex, was done.
Results
The results demonstrate that the number of training days
missed by an athlete due to self-reported sickness is nega-
tively correlated to the volume of training in a mixed
population of elite cross-country skiers, biathletes and
long-distance runners.
Subjects reported a total of 61 training years, had
trained an average of 462 (79-856) hours per year (medi-
an and range), were sick on 15 (0-164) days and injured
on 21 (0-164) days. The number of training years reported
was not significantly correlated to the number of self-
reported Exercise Constrained Sick Days reported (R2 =
0.33, p = 0.16) (Table 1).
Table 1. Group data on training volume and Exercise Con-
strained Sick Days in elite endurance athletes
Training Group
#TY
MECSD
10th and 90th percentile
< 266 h/year
12
54
18 and 160
266 - 538 h/year
27
17
6 and 57
> 538 h/year
22
8
0 and 27
#TY: Number of training years included. MECSD: Median Exercise
Constrained Sick Days
Training years are ranked from 1-61 according to
the number of training hours per year in Figure 1 (x-axis)
and plotted against the number of Exercise Constrained
Sick Days and the number of training hours in a dual y-
axis graph. Figure 1 shows that the number of training
hours per year is inversely correlated with the number and
variation in Exercise Constrained Sick Days.
A 3rd degree polynomial equation was derived (R2
= 0.48, p < 0.0001):
S = 37.5 - 0.048 * T + 0.00027*(T-453)2 - 5.6*10-7*(T-
453)3
where S is the number of sick days and T is the amount of train-
ing in hours.
This function is plotted in Figure 2 as a solid line,
with the area between the 95% Confidence Intervals (CI)
Mårtensson et al.
coloured grey and the 95% CI for individual data points
shown as dashed lines (Figure 2).
Figure 1. Sick days per year on left y-axis (solid line) and
Training hours per year on right y-axis (dashed line) plotted
against Individual training years on the x-axis. The variation
in the number of sick days falls at approximately 400 train-
ing hours, indicating that, the number of sick days per year
must be below 50 in order to train more than 400 hours per
year.
Figure 2. A third-degree polynomial bivariate fit (solid line)
of Sick days per year (y-axis) and Training hours per year
(x-axis) shows a significant (R2 = 0.48, F Ratio = 18, p <
0.0001, N = 61 training years from 11 subjects) decrease in
the number of sick days reported as the number of hours of
training increases. The shaded area indicates the 95% CI of
the model and the dashed lines indicate the 95% CI for the
individual data points.
The dataset of 61 individual training years was di-
vided into three groups based on the number of completed
hours of training using partition statistics to obtain the
maximum significance of the differences in the number of
ECDs between groups (Table 1). The skewness was 2.65,
and thus it was necessary to carry out log-transformation
of the ECD data. Loge (ECD) was then plotted along the
y-axis for the three groups (plotted as x-variable). Parti-
tion using Log transformed sick-days data resulted in
three groups; training less than 266 h/year (N = 12), train-
ing 266-538 h/year (N = 27) and training more than 538
h/year (N = 22). The non-parametric Kruskal-Wallis test
on non-transformed data gave Chi2 = 27, p < 0.0001 when
comparing number of sick days between the three training
groups, with median ECDs at 54 (10th percentile = 18,
90th percentile = 160), 17 (6, 57) and 8 (0, 27), respective-
Our results demonstrate that a high training load is ac-
companied by a low incidence of days of training lost due
to self-reported days of sickness, and is compatible with
our previous suggestion (Malm, 2006).
Our findings agree with those of Moreira et al.
(Moreira, Delgado, Moreira and Haahtela, 2009) in which
a combination of the classic J-curve proposed by Nieman
(1994a) and the S-curve proposed by Malm (2006) was
presented. The combined model suggests that the risk of
sickness in less-fit individuals can be displayed as a J-
curve, while the curve tends to flatten as fitness increases.
Moderate physical activity lowers the risk for infection in
non-athletic adults from that of inactive adults, which is
reflected in the J-curve nature of the results for such sub-
jects (Nieman, 1994b; Nieman et al., 2011). It may be
necessary to separate less-fit individuals from well-trained
individuals when interpreting the effects of exercise on
infection (Matthews et al., 2002), because of the demon-
strated increased self-reported upper respiratory tract
infection in elite, compared to recreational athletes
(Gleeson et al., 2013)
Many studies have examined endurance running
events such as marathons, and report that there is an in-
creased risk of acquiring an infection in the weeks follow-
ing such an event. However, Ilback et al. (1991) (in rats)
and Ekblom et al. (2006) (in humans) have shown that
pre-effort infection is the probable cause of the increase in
post-effort infection rates, not the post-effort sensitivity to
infections.
The present study did not investigate immune
function, but others have reported a different immune
response in elite compared to sedentary individuals
(Walsh et al., 2011). Different inclusion criteria could
therefore partly explain the difference in results between
the present and previous (Nieman, 1994a; 1994b) studies.
It can be argued that an immune system capable of
fighting infection also during and after repetitive, strenu-
ous exercise is necessary in order to become a successful
elite athlete. Thus, measurements of infection rates in elite
athletes are biased due to positive selection, and this could
explain the S-curve/flattened J-curve (Malm, 2006). Elite
athletes, such as the participants in this study, have the
ambition to train every healthy day, and thus more train-
ing hours can be completed in years with fewer infections.
These arguments are not in contradiction to such findings
as by Spence et al. (Spence et al., 2007), showing that
elite athletes have higher reported episodes of infections
than non-elite subjects. All athletes participating in the
present study performed at an elite level in their sport, and
had the ambition to reach high training volumes every
year in order to compete on a national and international
elite level; they were all accepted to the School of Sports
Science at Umeå University. However, because of infec-
tions, they were not able to reach their goals every season,
ly.
Discussion
Infections in elite athletes
932
manifested as the data points at the low end of Training
hours per year in Figure 2. Thus, the argument that infec-
tions caused low training volumes, may be equally valid
as the opposite; that high training volumes will cause
infections. The latter being practically and statistically
impossible, as 500-800 training hours per year will de-
mand very few sick days, regardless cause and pathology.
Consequently, a large variation in the number of sick days
will be present in any study including elite athletes, unless
a biased selection of only health elite subjects is done.
The results in the present study do not by any
means explain the cause, but are in line with our pilot
study (Malm, 2006) as well as our conclusion regarding
infection rates in marathon runners (Ekblom et al., 2006);
In elite athletes, exercise load is negatively correlated
with self-diagnosed Exercise Constrained Sick Days. A
recent review by Moreira et al. (2009) also conclude that
“among elite athletes, the relationship between exercise
load and immune dysfunction tends to flat”. The demands
associated with elite sports require an immune system that
is capable of fighting off infections also in situations with
extreme physical and mental challenges.
Because this study is based on retrospectively
summarize training logs, self-reported sickness, and a
relatively few athletes, future studies should include a
much larger number of subjects, as well as pathogen iden-
tification to investigate the mechanisms that govern the
immunological response and clinical outcome of exercise
training and competition. Of interested would also be to
correlate sick days and training volumes to diet, perfor-
mance and other co-founding factors in a prospective
approach. This could benefit our understanding not only
of the mechanisms behind the function of the immune
system, and its adaptation in elite athletes, but also the
clinical application of exercise to optimize both immune
function and performance.
Perspective
Elite athletes are individuals in pursuit of reaching their
genetic limits of physical performance. They encounter
numerous obstacles on this pathway, injuries and disease
being two of the most common. This study makes a sim-
ple, but not scientifically published, observation that min-
imizing the number of Exercise Constrained Sick Days is
a key issue for high training volumes in elite athletes,
whose key to winning is maintained health.
Conclusion
In elite athletes, high training volumes are incompatible
with a high number of non-training days, regardless of
cause. Consequently, the correlation between the number
of sick days and training hours was found to be negative.
References
Brines, R., Hoffman-Goetz, L. and Pedersen, B.K. (1996) Can you
exercise to make your immune system fitter? Immunology To-
day 17(6), 252-254
Dhabhar, F.S. (2014) Effects of stress on immune function: the good, the
bad, and the beautiful. Immunology Research 58(2-3), 193-210.
Ekblom, B., Ekblom, O. and Malm, C. (2006) Infectious episodes before
and after a marathon race. Scandinavian Journal of Medicine
and Science in Sports 16(4), 287-293.
Gleeson, M. (2007) Immune function in sport and exercise. Journal of
Applied Physiology 103(2), 693-699.
Gleeson, M., Bishop, N., Oliveira, M. and Tauler, P. (2013) Influence of
training load on upper respiratory tract infection incidence and
antigen-stimulated cytokine production. Scandinavian Journal
of Medicine and Science in Sports 23(4), 451-457.
Gleeson, M. and Walsh, N.P. (2012) The BASES expert statement on
exercise, immunity, and infection. Journal of Sports Science
30(3), 321-324.
Harriss, D.J. and Atkinson, G. (2011) Update - ethical standards in sport
and exercise science research. International Journal of Sports
Medicine 32(11), 819-821.
Heath, G.W., Ford, E.S., Craven, T.E., Macera, C.A., Jackson, K.L. and
Pate, R.R. (1991) Exercise and the incidence of upper respirato-
ry tract infections. Medicine and Science in Sports and Exercise
23(2), 152-157.
Ilback, N.G., Crawford, D.J., Neufeld, H.A. and Friman, G. (1991) Does
exercise stress alter susceptibility to bacterial infections? Upp-
sala Journal of Medicine and Science 96(1), 63-68
Malm, C. (2006) Susceptibility to infections in elite athletes: the S-
curve. Scandinavian Journal of Medicine and Science in Sports
16(1), 4-6.
Matthews, C.E., Ockene, I.S., Freedson, P.S., Rosal, M.C., Merriam,
P.A. and Hebert, J.R. (2002) Moderate to vigorous physical ac-
tivity and risk of upper-respiratory tract infection. Medicine and
Science in Sports and Exercise 34(8), 1242-1248.
Moreira, A., Delgado, L., Moreira, P. and Haahtela, T. (2009) Does
exercise increase the risk of upper respiratory tract infections?
British Medical Bulletin 90, 111-131.
Nieman, D.C. (1994a) Exercise, infection, and immunity. International
Journal of Sports Medicine 15 (Suppl 3), S131-141.
Nieman, D.C. (1994b) Exercise, upper respiratory tract infection, and
the immune system. Medicine and Science in Sports and Exer-
cise 26(2), 128-139.
Nieman, D.C. (1997) Risk of upper respiratory tract infection in athletes:
An epidemiologic and immunologic perspective. Journal of
Athletic Training 32(4), 344-349.
Nieman, D.C. (2003) Current perspective on exercise immunology.
Current Sports Medicine Reports 2(5), 239-242.
Nieman, D.C., Henson, D.A., Austin, M.D. and Sha, W. (2011) Upper
respiratory tract infection is reduced in physically fit and active
adults. British Journal of Sports Medicine 45(12), 987-992.
Nieman, D.C., Johanssen, L.M. and Lee, J.W. (1989) Infectious epi-
sodes in runners before and after a roadrace. Journal of Sports
Medicine and Physical Fitness 29(3), 289-296.
Nieman, D.C., Johanssen, L.M., Lee, J.W. and Arabatzis, K. (1990)
Infectious episodes in runners before and after the Los Angeles
Marathon. Journal of Sports Medicine and Physical Fitness
30(3), 316-328.
Nieman, D.C., Nehlsen-Cannarella, S.L., Fagoaga, O.R., Henson, D.A.,
Shannon, M., Hjertman, J.M., Schmitt, R.L., Bolton, M.R:,
Austin, M.D., Schling, B.K. and Thorpe, R. (2000) Immune
function in female elite rowers and non-athletes. British Journal
of Sports Medicine 34(3), 181-187.
Pedersen, B.K. and Bruunsgaard, H. (1995) How physical exercise
influences the establishment of infections. Sports Medicine
19(6), 393-400.
Pedersen, B.K. and Ullum, H. (1994) NK cell response to physical
activity: possible mechanisms of action. Medicine and Science
in Sports and Exercise 26(2), 140-146.
Peters, E.M. and Bateman, E.D. (1983) Ultramarathon running and
upper respiratory tract infections. An epidemiological survey.
South African Medical Journal 64(15), 582-584.
Spence, L., Brown, W.J., Pyne, D.B., Nissen, M.D., Sloots, T.P.,
McCormack, J.G., Locke, A.S. and Fricker, P.A. (2007) Inci-
dence, etiology, and symptomatology of upper respiratory ill-
ness in elite athletes. Medicine and Science in Sports and Exer-
cise 39(4), 577-586.
Walsh, N. P., Gleeson, M., Pyne, D. B., Nieman, D. C., Dhabhar, F. S.,
Shephard, R. J., Oliver, S.J., Bermon, S. and Kajeniene, A.
(2011) Position statement. Part two: Maintaining immune
health. Exercise Immunology Review 17, 64-103.
Mårtensson et al.
Key points
Top level performance demands high training vol-
umes and intensities, which may compromise im-
mune function.
Elite athletes must have an immune system capable
of intact function also when under sever physiologi-
cal and psychological stress.
Elite performance, especially in endurance sports, is
therefore incompatible with a high rate of infections.
A negative correlation between infections and exer-
cise training load among elite athletes is consequent-
ly observed the less sick you are the more you can
train.
AUTHORS BIOGRAPHY
Sandra MÅRTENSSON
Employement
Sports Med
icine Unit, Umeå University,
Sweden
Degree
BSc
Research interest
Infection risk and elite athletes. Currently
working with health maintenance, exercise
training and diet.
E-mail: sandravm88@hotmail.com
Kristina NORDEBO
Employement
Sports Medicine Unit, Umeå University,
Sweden
Degree
MS
Research interest
Infections and adaptations to exercise.
E-mail: k_nordebo@hotmail.com
Christer MALM
Employement
Assoc. Prof., Sports Medicine Unit, Umeå
University, Sweden
Degree
PhD
Research interest
Muscle adaptation to exercise, immune
function, physical performance and testing.
E-mail: christer.malm@umu.se
Christer Malm
Sports Medicine Unit and School of Sports Sciences, Umeå
University, Sweden
... In addition, professional athletes eat more frequently in group canteens, where industrially produced meals are served using dishware and cutlery that have been cleaned with aggressive detergents(Figure 4).72 Elite athletes at the highest level, despite undergoing high training loads, may not necessarily show an increased risk of illness. This phenomenon could potentially be linked to their different behaviors that are more "protective" of the epithelial barrier, such as maintaining a strict hygiene regimen, optimal nutrition, adequate rest, and overall better immune system function due to their physical conditioning as well as better monitoring and treatment by medical professionals.73,74 Another important aspect of epithelial barrier theory is the circulating microinflammation as a response to environmental substances and the translocation of proinflammatory microbiota toward the subepithelial tissue. ...
Article
Full-text available
Exposure to toxic substances, introduced into our daily lives during industrialization and modernization, can disrupt the epithelial barriers in the skin, respiratory, and gastrointestinal systems, leading to microbial dysbiosis and inflammation. Athletes and physically active individuals are at increased risk of exposure to agents that damage the epithelial barriers and microbiome, and their extreme physical exercise exerts stress on many organs, resulting in tissue damage and inflammation. Epithelial barrier‐damaging substances include surfactants and enzymes in cleaning products, laundry and dishwasher detergents, chlorine in swimming pools, microplastics, air pollutants such as ozone, particulate matter, and diesel exhaust. Athletes' high‐calorie diet often relies on processed foods that may contain food emulsifiers and other additives that may cause epithelial barrier dysfunction and microbial dysbiosis. The type of the material used in the sport equipment and clothing and their extensive exposure may increase the inflammatory effects. Excessive travel‐related stress, sleep disturbances and different food and microbe exposure may represent additional factors. Here, we review the detrimental impact of toxic agents on epithelial barriers and microbiome; bring a new perspective on the factors affecting the health and performance of athletes and physically active individuals.
... According to a survey of the 2002 Asian Games' Japan National Team, 26.8% of the players experienced deterioration of physical condition before a match, 29.4% of whom had actually been affected during a match (1). A survey of top cross-country athletes showed a negative correlation between the number of days of infection and the practice time, suggesting that deterioration of physical condition could lead to a loss of practice time and poor athletic performance (2). As a countermeasure against deterioration of physical condition, daily maintenance of immune function and sufficient recovery after exercise are needed. ...
Article
Background: Whole-body cryotherapy (WBC) is used as a conditioning method for athletes. However, the scientific evidence for its effects is still insufficient. Objective: To elucidate the effects of transient WBC on the expression of heat shock protein (HSP) 70 and the secretion of related hormones in humans. Materials and methods: The participants in this study were six healthy adult men. WBC was performed for 3 min in a booth at a temperature in the range of -150 to -120 degree C, and measurements were taken immediately before (Pre), immediately after (Post), and 60 min after WBC (Post60). For measurement of core body temperature (gastrointestinal temperature), participants ingested a capsule-type wireless temperature sensor. The body surface temperature was measured using a noncontact thermometer, and measurements were taken at four sites on the body surface (chest, abdomen, front of the thigh, and front of the lower thigh). Leukocyte count, lactate dehydrogenase, creatine kinase, hemoglobin, hematocrit, adrenaline, noradrenaline, cortisol, adrenocorticotropic hormone (ACTH), erythropoietin, and HSP70 in the collected blood were measured. Results: The results showed a decrease in body surface temperature and an increase in noradrenaline and ACTH immediately after WBC. In addition, the core body temperature decreased 60 min after WBC, accompanied by an increase in HSP70 expression. Conclusion: WBC may increase HSP70 expression via noradrenaline and ACTH. The results of this study suggest the usefulness of WBC in triggering protein synthesis and the maintenance of immune function after training. doi.org/10.54680/fr22210110512.
... 105 A more recent modification based on previous reports on increased infection rate in athletes reporting pre-race symptoms is that the relationship may be more "S-shaped". 106 Exercise may well have a significant effect on the microbiome. ...
Article
Full-text available
This review presents state‐of‐the‐art knowledge and identifies knowledge gaps for future research in the area of exercise‐associated modifications of infection susceptibility. Regular moderate‐intensity exercise is believed to have beneficial effects on immune health through lowering inflammation intensity and reducing susceptibility to respiratory infections. However, strenuous exercise, as performed by professional athletes, may promote infection: in about half of athletes presenting respiratory symptoms, no causative pathogen can be identified. Acute bouts of exercise enhance the release of pro‐inflammatory mediators, which may induce infection‐like respiratory symptoms. Relatively few studies have assessed the influence of regularly repeated exercise on the immune response and systemic inflammation compared to the effects of acute exercise. Additionally, ambient and environmental conditions may modify the systemic inflammatory response and infection susceptibility, particularly in outdoor athletes. Both acute and chronic regular exercise influence humoral and cellular immune response mechanisms, resulting in decreased specific and non‐specific response in competitive athletes. The most promising areas of further research in exercise immunology include detailed immunological characterization of infection‐prone and infection‐resistant athletes, examining the efficacy of nutritional and pharmaceutical interventions as countermeasures to infection symptoms, and determining the influence of various exercise loads on susceptibility to infections with respiratory viruses, including SARS‐CoV‐2. By establishing a uniform definition of an “elite athlete,” it will be possible to make a comparable and straightforward interpretation of data from different studies and settings.
Article
Purpose This study aimed to determine the effects of yoga on the recovery of the cardiac autonomic nervous system and immunosuppression after intense exercise. Methods Seven healthy adult men were enrolled in two trials: rest for 30 min in a seated position (CON) and yoga for 30 min (YOG) after a treadmill running for 60 min at 75% O 2max in a randomized crossover design. Natural killer (NK) cell activity, salivary secretory immunoglobulin A (SIgA), cortisol, testosterone, and indicators related to heart rate variability, mood states, and muscle soreness were measured before exercise (Pre), immediately (P0) and 60 min (P1) after rest or yoga, and the following morning (P2). Results NK cell activity was significantly decreased in the CON trial ( P < 0.05) but not in the YOG trial. The decrease in NK cell activity from Pre at P0, P1, and P2 in the CON trial was significantly larger than that in the YOG trial ( P < 0.05). Testosterone secretion rate tended to be higher after yoga than at rest ( P = 0.052). The square root of the mean squared difference of successive normal-to-normal intervals (RMSSD) at P0 in the YOG trial was significantly higher than that in the CON trial ( P < 0.05). Changes in NK cell activity correlated with changes in RMSSD ( r = 0.445, P < 0.05). Conclusion This study showed that yoga can alleviate the decline of NK cell activity after intense exercise by enhancing parasympathetic nerve activity, thus suggesting that yoga may be an effective recovery method for athlete conditioning.
Article
Full-text available
Domestic horses routinely participate in vigorous and various athletic activities. This enables the horse to serve as a model for studying athletic physiology and immunology in other species, including humans. For instance, as a model of physical efforts, such as endurance rides (long-distance running/aerobic exercise) and races (anaerobic exercise), the horse can be useful in evaluating post-exercise response. Currently, there has been significant interest in finding biomarkers, which characterize the advancement of training and adaptation to physical exercise in the horse. The parallels in cellular responses to physical exercises, such as changes in receptor expression and blood cell activity, improve our understanding of the mechanisms involved in the body’s response to intense physical activity. This study focuses on the changes in levels of the pro- and anti-inflammatory cytokines and cellular response in the context of post-exercise immune response. Both the direction of changes in cytokine levels and cellular responses of the body, such as proliferation and expression of surface markers on lymphocytes, monocytes and neutrophils, show cross-functional similarities. This review reveals that horses are robust research models for studying the immune response to physical exercise in human athletes.
Article
Full-text available
The benefits of physical activity and exercise, especially those classified as moderate-to-vigorous activity (MVPA), have been well-established in preventing non-communicable diseases and mental health problems in healthy adults. However, the relationship between physical activity and exercise and the prevention and management of acute respiratory infection (ARI), a global high-burden disease, has been inconclusive. There have been debates and disagreements among scientific publications regarding the relationship between exercise and immune response against the causative agents of ARI. This narrative review aims to explore the theory that sufficiently explains the correlation between exercise, immune response, and ARI. The potential root causes of discrepancies come from research associated with the “open window” hypothesis. The studies have several limitations, and future improvements to address them are urgently needed in the study design, data collection, exercise intervention, subject recruitment, biomarkers for infection and inflammation, nutritional and metabolism status, and in addressing confounding variables. In conclusion, data support the clinical advantages of exercise have a regulatory contribution toward improving the immune response, which in turn potentially protects humans fromARI. However, the hypothesis related to its negative effect must be adopted cautiously.
Chapter
Exercise immunology is the field that studies the effects of exercise on the immune system. In the 1990s, Dr. Nieman formulated the controversial “J-shaped hypothesis” to describe the relationship between acute exercise intensity and the risk of acquiring infections, such as upper respiratory tract infections. This hypothesis suggested that moderate exercise has the ability to improve immune function above sedentary levels, while high intensity exercise depresses the immune system. Since then, current knowledge has exposed some methodological limitations, challenging the idea that any form of exercise can be considered “immunosuppressive”. Overall, acute bouts of moderate exercise have shown to enhance immune-surveillance, while frequent exercise has been associated with an increased immunological competency. Actually, contemporary research interests are focused in understand how immune changes induced by exercise are able to reduce risk for common chronic diseases. To this end, the introduction of -omics approaches (metabolomics, proteomics, lipidomics, and metagenomics) is providing new insights on the interactions between exercise and immunity. In this chapter, we deep into the previous literature addressing the “immunity-exercise axis” in order to critically review the basis of the J-shaped curve and open window hypothesis. In addition, an overview of the components of the immune system and how are affected by exercise considering the gender dimension will help us to unravel the key role of regular physical activity in the prevention and treatment of disease.
Article
Full-text available
Exercise and nutrition, when used as a mode to improve health outcomes is well-researched and accepted by researchers and clinicians, alike. Numerous health organizations have developed general recommendations such as physical activity and exercise to inform the public how to improve health outcomes. More often than not, these guidelines are vague and do not suggest how to achieve optimal health via exercise and nutrition. These guidelines also fail to consider physiological and psychological variability for patients and individuals aiming to follow such guidelines. For example, current recommendations include exercise intensities based on low, moderate, and vigorous activity and many people may not understand the physiological cost of such exercise intensities. Presently, accessible consumer-grade technology allows for accurate measurements of relative heart rate, exercise time, distance, and estimated caloric expenditure which is presumed easy for any person to understand. Therefore, creating guidelines that target specific and measurable variables, such as relative heart rate may be more advantageous for individualized health optimization.
Article
Full-text available
An individual's level of physical activity influences their risk of infection, most likely by affecting immune function. Regular moderate exercise reduces the risk of infection compared with a sedentary lifestyle, but very prolonged bouts of exercise and periods of intensified training are associated with an increased risk of infection. There are several lifestyle, nutritional, and training strategies that can be adopted to limit the extent of exercise-induced immunodepression and minimize the risk of infection. This expert statement provides a background summarizing the evidence together with extensive conclusions and practical guidelines.
Article
Full-text available
The physical training undertaken by athletes is one of a set of lifestyle or behavioural factors that can influence immune function, health and ultimately exercise performance. Others factors including potential exposure to pathogens, health status, lifestyle behaviours, sleep and recovery, nutrition and psychosocial issues, need to be considered alongside the physical demands of an athlete's training programme. The general consensus on managing training to maintain immune health is to start with a programme of low to moderate volume and intensity; employ a gradual and periodised increase in training volumes and loads; add variety to limit training monotony and stress; avoid excessively heavy training loads that could lead to exhaustion, illness or injury; include non-specific cross-training to offset staleness; ensure sufficient rest and recovery; and instigate a testing programme for identifying signs of performance deterioration and manifestations of physical stress. Inter-individual variability in immunocompetence, recovery, exercise capacity, non-training stress factors, and stress tolerance likely explains the different vulnerability of athletes to illness. Most athletes should be able to train with high loads provided their programme includes strategies devised to control the overall strain and stress. Athletes, coaches and medical personnel should be alert to periods of increased risk of illness (e.g. intensive training weeks, the taper period prior to competition, and during competition) and pay particular attention to recovery and nutritional strategies.
Article
Full-text available
Heavy exercise induces marked immunodepression, which is multifactorial in origin. Evidence showing clinical significance of this immunodepression is scarce. We assessed in a systematic manner whether physical activity or intensity of exercise increase susceptibility to upper respiratory tract infections (URTI). A literature search was performed using the keywords 'upper respiratory tract infections', 'athletes', 'exercise' and 'physical activity'. We considered all studies reporting of the effect of exercise, physical activity, sport and training on susceptibility to URTI. A total of 162 publications were identified and 30 studies were eligible (4 descriptive, 18 observational and 8 interventional). The 30 studies included 8595 athletes (5471 runners, 2803 swimmers) and 1798 non-athletes. Moderate activity may enhance immune function, whereas prolonged, high-intensity exercise temporarily impairs the immune competence. Athletes, when compared with lesser active individuals, experience higher rate of URTI after training and competitions. In non-athletes, increasing physical activity is associated with a decreased risk of URTI. The relationship between exercise and URTI is affected by poorly known individual determinants such as genetic factors, fitness, nutritional status or atopy. Elite athletes may have a decreased susceptibility to URTI. The dose-response relationship between immunodepression and risk for URTI during the weeks following heavy exercise. What are the clinically relevant methods to assess exercise-induced immunodepression? Is down-regulation of immunity after intense exercise a protective response to limit inflammation? Is there a role for nutritional or pharmaceutical interventions to reduce risk of URTI?
Article
Full-text available
Swimming was used for evaluating alterations in performance capacity and as a means for studying the influence of exercise stress on susceptibility to Streptococcus pneumoniae and Francisella tularensis infections in two strains of rats, i.e. Fisher-Dunning (FD) and Sprague-Dawley (SD). The performance capacity was reduced by both diseases and was correlated to the dose of the given micro-organism. FD rats, however, were more susceptible to the infection and showed a greater deterioration than SD rats. The effects of exercise stress on disease lethality varied with the time that it was performed. Strenuous exercise immediately before infection drastically reduced susceptibility to either of the bacteria, while a similar bout of exercise performed after infection increased disease-related mortality in both diseases.
Article
Although the concept of stress has earned a bad reputation, it is important to recognize that the adaptive purpose of a physiological stress response is to promote survival during fight or flight. While long-term stress is generally harmful, short-term stress can be protective as it prepares the organism to deal with challenges. This review discusses the immune effects of biological stress responses that can be induced by psychological, physiological, or physical (including exercise) stressors. We have proposed that short-term stress is one of the nature's fundamental but under-appreciated survival mechanisms that could be clinically harnessed to enhance immunoprotection. Short-term (i.e., lasting for minutes to hours) stress experienced during immune activation enhances innate/primary and adaptive/secondary immune responses. Mechanisms of immuno-enhancement include changes in dendritic cell, neutrophil, macrophage, and lymphocyte trafficking, maturation, and function as well as local and systemic production of cytokines. In contrast, long-term stress suppresses or dysregulates innate and adaptive immune responses by altering the Type 1-Type 2 cytokine balance, inducing low-grade chronic inflammation, and suppressing numbers, trafficking, and function of immunoprotective cells. Chronic stress may also increase susceptibility to some types of cancer by suppressing Type 1 cytokines and protective T cells and increasing regulatory/suppressor T cell function. Here, we classify immune responses as being protective, pathological, or regulatory, and discuss "good" versus "bad" effects of stress on health. Thus, short-term stress can enhance the acquisition and/or expression of immunoprotective (wound healing, vaccination, anti-infectious agent, anti-tumor) or immuno-pathological (pro-inflammatory, autoimmune) responses. In contrast, chronic stress can suppress protective immune responses and/or exacerbate pathological immune responses. Studies such as the ones discussed here could provide mechanistic targets and conceptual frameworks for pharmacological and/or biobehavioral interventions designed to enhance the effects of "good" stress, minimize the effects of "bad" stress, and maximally promote health and healing.
Article
This study examined the effect of training load on upper respiratory tract infection (URTI) incidence in men and women engaged in endurance-based physical activity during winter and sought to establish if there are training-associated differences in immune function related to patterns of illness. Seventy-five individuals provided resting blood and saliva samples for determination of markers of systemic immunity. Weekly training and illness logs were kept for the following 4 months. Comparisons were made between subjects (n = 25) who reported that they exercised 3-6 h/week (LOW), 7-10 h/week (MED) or ≥ 11 h/week (HIGH). The HIGH and MED groups had more URTI episodes than the LOW group (2.4 ± 2.8 and 2.6 ± 2.2 vs 1.0 ± 1.6, respectively: P < 0.05). The HIGH group had approximately threefold higher interleukin (IL)-2, IL-4 and IL-10 production (all P < 0.05) by antigen-stimulated whole blood culture than the LOW group and the MED group had twofold higher IL-10 production than the LOW group (P < 0.05). Other immune variables were not influenced by training load. It is concluded that high levels of physical activity are associated with increased risk of URTI and this may be related to an elevated anti-inflammatory cytokine response to antigen challenge.
Article
Limited data imply an inverse relationship between physical activity or fitness level and the rates of upper respiratory tract infection (URTI). The purpose of this study was to monitor URTI symptoms and severity in a heterogeneous group of community adults and contrast across tertiles of physical activity and fitness levels while adjusting for potential confounders. A group of 1002 adults (ages 18-85 years, 60% female, 40% male) were followed for 12 weeks during the winter and fall seasons while monitoring URTI symptoms and severity using the Wisconsin Upper Respiratory Symptom Survey. Subjects reported frequency of aerobic activity, and rated their physical fitness level using a 10-point Likert scale. A general linear model, with adjustment for seven confounders, was used to examine the effect of exercise frequency and fitness level on the number of days with URTI and severity of symptoms. The number of days with URTI during the 12-week period was significantly reduced, 43% in subjects reporting ≥ 5 days/week aerobic exercise compared to those who were largely sedentary (≤ 1 day/week) and 46% when comparing subjects in the high versus low fitness tertile. URTI severity and symptomatology were also reduced 32% to 41% between high and low aerobic activity and physical fitness tertiles. Perceived physical fitness and frequency of aerobic exercise are important correlates of reduced days with URTI and severity of symptoms during the winter and fall common cold seasons.
Article
We examined illness patterns in a cohort of 530 male and female runners who completed a monthly log for 12 months. The average number of upper respiratory tract infections (URTIs) per person per year for the cohort was 1.2. An upper respiratory tract infection was indicated by the report of any of the following symptoms; runny nose, sore throat, or cough. Using a multiple logistic regression model, the following factors were found to be associated with having one or more URTIs in the follow-up period: living alone (odds ratio = 2.27, 95% CI = 1.01, 5.09), running mileage (486-865 miles, odds ratio = 2.00, 95% CI = 1.01, 2.78; 866-1388 miles, odds ratio = 3.50, 95% CI = 1.52, 4.44; greater than 1388 miles, odds ratio = 2.96, 95% CI = 1.30, 3.68), body mass index greater than the 75th percentile (odds ratio = 0.58, 95% CI = 0.35, 0.94), and male gender (odds ratio = 0.14, 95% CI = 0.03, 0.68). A significant interaction was found to exist between gender and alcohol use, with the association between alcohol use and upper respiratory tract infections being positive in males and negative in females. These results suggest that running dosage (mileage) is a significant risk factor for upper respiratory tract infections in this group of exercisers.