Introduction
The negative influence of acute toothache on top athletic performance is considered
generally obvious and has been described in sporadic publications [1]. Moreover, oral diseases can interact with
the entire body system. Although the relevance for professional sports must still
be
determined, there is a potential risk of a negative influence on performance [2]. Accordingly, oral health should play a role
in professional sports. However, a high prevalence of oral inflammation was stated
in elite athletes [1]
[3]
[4].
Based on existing data, neither Olympic athletes [3]
[5] nor athletes in
well-sponsored sports, e. g., soccer [6], seem to receive adequate dental care [6].
Up to now, the reasons for the deficiencies in oral health in elite athletes have
not
been fully understood. On the one hand, physical stress and accompanying parameters
could influence oral health behavior leading to effects on oral health status. On
the other hand, physical stress itself could have direct effects on oral tissues.
Owing to their prevalence and potential systemic interactions, inflammatory oral
diseases have special importance in this respect [7].
The aim of the present review is an overview of the most common types of oral
inflammation, their prevalence, significance for performance, and causes in elite
athletes. Possible mechanisms of bidirectional interaction between competitive
sports and oral health will be presented.
Types of oral inflammation ([Table 1],
[Fig. 1])
Fig. 1 Clinical and radiographic impressions of different types of
oral inflammation: Gingivitis (a–c), (marginal)
periodontitis (d–f), pericoronitis
(g–j), apical periodontitis
(k–n). a–c) Gingivitis:
Redness and swelling (S) of the gingiva indicate acute inflammation and
probing or even toothbrushing often results in bleeding (b,
c). Note the causal dental plaque-biofilm (B) at the gingival
margin and the dental calculus (C). d–f)
(Marginal) Periodontitis: The inflammation of the tooth-supporting
tissues (periodontium) leads to its destruction. The resulting
attachment loss is clinically visible as resulting recessions (R) with
exposed root surfaces (d, f). The corresponding
radiography (e) allows the evaluation of the extent of the
interdental bone loss. g–j) Pericoronitis:
Remaining tissue partially covers the wisdom tooth (W) and leads to a
niche (g). The corresponding radiography (h) shows a
correct vertical position but an anatomic position in the ascending part
of the mandibula. Also, a clinical unerupted wisdom tooth (W) can lead
to niche and subsequent inflammation (i). The radiography
(j) shows the connection to the oral cavity and an angular
dislocation that inhibits the eruption. k–n)
Apical periodontitis: The typical radiographic manifestation of chronic
apical periodontitis (k) shows a clearly visible periapical bone
lesion (L). After dental trauma, apical resorption (D) can occur
(l). An intraoral visible fistulae (F) drainages pus from an
exacerbated apical inflammatory process (m). The radiography
(n) shows resorption (D) of the root apex of the tooth with
insufficient root canal treatment. Source for [Fig 1d]: Dr. Elena
Günther. Source for [Fig
1g] and [Fig 1m]:
Tilman Riemer.
Table 1 Survey of the most frequent types of oral
inflammation including symptoms, potential influence on performance,
and approaches for therapy and prevention.
|
Gingivitis
|
Periodontitis
|
Pulpitis/Periodontitis apicalis
|
Pericoronitis
|
|
Symptoms
|
Bleeding, swelling, pseudo pockets
|
Pocket formation, bone loss
|
Toothache
|
Pain, swelling, sometimes fever
|
|
Systemic influence (performance or regeneration)
|
+
|
+++
|
++
|
++
|
|
Possible causes for missing training/competition
|
–
|
(+)
|
++
|
++
|
|
Therapy
|
Prophylaxis, antiseptic mouth wash, improved intense
individual oral hygiene
|
Repeated prophylaxis, periodontal therapy with subgingival
cleaning
|
Root canal treatment, pain medication if applicable
|
If applicable, pain medication, local anti-inflammatory
therapy, recess removal by removal of soft tissue or wisdom
tooth
|
|
Prevention
|
Adequate oral hygiene, individual preventive dental care
|
Regular screening, individual preventive dental care
|
Regular dental examinations, especially presentation after
traumata
|
Regular clinical and radiological evaluation of the
situation, removal of wisdom teeth if applicable
|
+ The number of plus signs presents the probability from
+ for possible up to +++ for very
likely. – A minus sign signifies unlikelihood.
Inflammation of tissues around teeth, e. g., gingivitis, is common,
affecting more than 90% of the global population [8]
[9]. The most common type is dental plaque biofilm-induced gingivitis
([Fig. 1a–c]), which affects
the gingiva only. This non-specific inflammatory condition is caused by
accumulated plaque biofilm at and below the gingival margin [10]. The typical clinical signs are
erythema, edema, bleeding (especially during tooth brushing), and enlargement,
but usually no pain [10]. This disease is
fully reversible after biofilm removal [11]. It is known that systemic conditions such as pregnancy and
micronutrient deficiencies can favor this type of oral inflammation [11].
Gingivitis is a prerequisite for periodontitis [11]. Persistent gingivitis can progress into inflammation of the
entire periodontium (the tooth-supporting tissues) ([Fig. 1d–f]) [12]
[13]
[14]. While approximately
only 1.7% of the population aged up to 25 years is affected [15], more than 50% of the
population aged 35 to 44 and 90% of older adults experience
periodontitis [16]. Severe developments
are estimated to affect 5 to 15% of the global population [8]. Today, periodontitis is considered a
multifactorial and primarily polybacterial opportunistic infectious disease of
the periodontium [17]
[18]. The clinical manifestation of the
disease covers a depth proliferation of the gingival pockets and ulceration of
the dental epithelium, resulting in a reduction of periodontium and bone
(so-called attachment loss). Chronologically, periodontitis is accompanied by an
increasing accumulation of potentially periodontopathic bacteria (subgingival
biofilms). The versatile interactions between biofilms and hosts play a key
role. The transition from periodontal health to periodontitis is marked by
imbalances in the biofilm (ecologic shift, dysbiosis) and subsequent between the
host and biofilm (immunological disbalance) [17]. The dysbiotic state includes an increase in gram-negative,
obligatory anaerobic microorganisms such as Porphyromonas gingivalis,
Tanerella forsythia, and Treponema denticola
[19]. They undermine the immune defense of
the host by different virulence factors and cause inflammatory reactions [20]. The induced (partly overactive) immune
reaction influences connective tissue metabolism and bone metabolism [20]. Alveolar bone degradation with the
formation of gingival pockets leads to the typical clinical picture of
periodontitis. In cases with continuing progression, tooth mobility and tooth
loss may occur. Usually, the disease is free of pain. Nevertheless, the
resulting inflammatory surface can reach a considerable surface of more than
2,000 mm² [21].
Another type of oral inflammation that may occur around partially erupted teeth
is pericoronitis ([Fig. 1g–j]).
Plaque retention and food impact favor the inflammation of the tissue around the
tooth crown [22]. The breakthrough of
wisdom teeth is expected in their late teens or early 20s. In many people, there
is not enough space for wisdom teeth, or they are dislocated and thus cannot
grow in the normal dentition. Therefore, approximately 25% of the adult
population is diagnosed with impacted wisdom teeth [23]. Approximately 5% experience
pericoronitis, especially at ages 21 to 25 [24]. While chronic pericoronitis (83%) generally has a
subclinical development, subjects with acute pericoronitis (12%) suffer
severe pain, distinct swelling, and general symptoms such as fever or even
spreading of the inflammation, e. g., abscesses. Symptomatic
pericoronitis can affect oral functions such as nutrition as well as lifestyle
and sleep [25].
Moreover, pulpitis (inflammation of the tooth nerve), and apical periodontitis
(inflammation around the root apex of a tooth) must be mentioned ([Fig. 1k–n]). Pulpitis and acute
apical periodontitis can cause severe pain. Chronic apical periodontitis can
involve no or only minor symptoms. In cases with exacerbation, abscesses may
lead to spreading with accompanying general symptoms. Irreversible pulpitis is
described in approximately 1% of teeth [26], apical periodontitis is an issue in approximately 50% of
the adult population [27], and acute
exacerbation is only present in less than 5% [28]. Root canal treatment of the affected
tooth is required to treat these conditions. These inflammations may originate
from extended carious lesions but also from tooth trauma.
State of oral inflammation in athletes ([Table 2])
Table 2 State of oral inflammation in elite athletes
including prevalences according to published contemporary data (time
of evaluation not before the year 2003). Data from dental clinics
during competitions were excluded due to high selection
bias.
|
State of oral inflammation in elite athletes
|
|
Oral inflammation
|
Prevalence
|
Cohort
|
References
|
|
Gingivitis
|
|
Gingival bleeding (self-reported)
|
30–60%
|
Professional soccer players, elite athletes in Great Britain,
endurance athletes from German perspective, and youth
squads
|
Gay-Escoda 2011 [6],
Gallagher et al. 2018 [29], Merle et al. 2022 [31]
|
|
Signs of gingivitis (PSI score 1 or 2)a
|
60–97%
|
Elite athletes in Great Britain, Dutch candidates for the
Olympic Games 2016, endurance athletes from German
perspective, and youth squads
|
Needleman et al. 2016 [30], Gallagher et al. 2018 [29], Kragt et al. 2019
[3], Merle et al.
2022 [31]
|
|
Gingivitis (no detailed definition)
|
58–64%
|
Professional rugby players, Dutch candidates for the Olympic
Games 2016, endurance athletes from German perspective, and
youth squads
|
Minty et al. 2018 [41],
Kragt et al. 2019 [3],
Merle et al. 2022 [31]
|
|
Periodontitis
|
|
|
|
|
Signs of periodontitis (PSI score 3 or 4)a
|
5–40%
|
Elite athletes in Great Britain, Dutch candidates for the
Olympic Games 2016, endurance athletes from German
perspective, and youth squads
|
Needleman et al. 2016 [30], Gallagher et al. 2018 [29], Kragt et al. 2019
[3], Merle et al.
2022 [31]
|
|
Periodontitisb
Stage I
Stage II
Stage III
|
41%
32%
5%
5%
|
Professional soccer players
|
Botelho et al. 2021 [4]
|
|
Pericoronitis
|
|
|
|
|
Problems with wisdom teeth (self-reported)
|
14–23%
|
Elite athletes in Great Britain
|
Needleman et al. 2016 [30], Gallagher et al. 2018 [29]
|
|
Acute pericoronitis
|
1–3%
|
Elite athletes in Great Britain
|
Needleman et al. 2016 [30], Gallagher et al. 2018 [29]
|
|
Recommendation for removal of at least one wisdom tooth
|
22%
|
Dutch candidates for the Olympic Games 2016
|
Kragt et al. 2019 [3]
|
|
Other inflammation
|
|
|
|
|
Need for root canal treatment
|
2–24%
|
Athletes in the Middle East (Qatar), Dutch candidates for the
Olympic Games 2016
|
Knight et al. 2019 [34], Kragt et al. 2019 [3],
|
|
Open pulp, ulceration, fistula, or abscess
|
3–8%
|
Elite athletes in Great Britain
|
Needleman et al. 2016 [30], Gallagher et al. 2018 [29]
|
Oral health in athletes has not yet been sufficiently evaluated. Existing studies
on oral inflammation in elite athletes generally show a high prevalence of
gingivitis (58–97%)
[3]
[5]
[29]
[30]. The stated prevalence of periodontitis
is lower (5–41%) [3]
[5]
[29]
[30]
[31]
[32]. When interpreting these data, it must be considered that these
studies often indicate the prevalence of periodontitis, but usually used the
surrogate marker necessity of periodontal treatment. The examinations were
screenings (Periodontal Screening Index [33], PSI, basic periodontal examination, or Dutch periodontal
screening index, score 3 or 4) that can only state the presence of increased
periodontal probing depths (PPDs) and the resulting necessity of individual
preventive care and periodontitis therapy where appropriate. A diagnosis of
periodontitis is not possible with the collected data. Only one study provides a
detailed examination of the periodontal situation: In soccer players with a mean
age of 28 years, periodontitis was diagnosed in 41% of the subjects,
mainly as initial forms (32%) (stage I with attachment loss up to max.
of 2 mm) with only one case of moderate (stage II, 3–4 mm) and one of
severe periodontitis (stage III, ≥ 5 mm) [4]. Clinical experience shows pronounced
findings of oral inflammation even in young, generally healthy, sport-active
patients ([Fig. 2]). A study comparing
competitive and amateur athletes allow the assumption of an increased
periodontitis prevalence in young adult elite athletes [31].
Fig. 2
a and b Example of periodontal damage in young years: This
young, systemically healthy, active sporting woman showed localized
severe periodontitis in her early 20s. (a) Clinical situation
with only slight signs of recession (R) mesial of 46. The external
appearance may seem healthy at the first glance. A screening by probing
revealed the periodontal pocket. (b) The radiograph shows the
extent of periodontal damage: The vertical bone defect (BD) mesial of 46
reaches up to the middle of the root.
Regarding wisdom teeth-related inflammation, a total of 14 to 23% of the
athletes reported corresponding discomfort [29]
[30]; up to 3%
showed clinical signs of pericoronitis, and in 22% removal of at least
one wisdom tooth was recommended [3].
Moreover, pronounced acute oral inflammation such as open pulp, ulcerations,
fistulas, or abscesses were found in 3 to 8% of elite athletes [29]
[30]. Periapical infections were recorded in 12% of athletes
in the Middle East [34]. In general, they
are a frequent reason for dental consultations in the Olympic Games [35]
[36]
[37]
[38].
For interpretation of these data, it must be considered that (partially small)
cohorts in different types of sports and different countries have been
evaluated. Sport disciplines show a high variety of resulting influence factors
and behaviors. Differences include for example body composition and nutrition
behavior [39]. The categorization in
endurance, strength, contact, and team sport might provide an initial
estimation. Oral health behavior, socioeconomic status, [40] and the health care system, which
depend on the athlete’s country of origin and the country of
investigation, might have a further impact. These points limit comparability and
transferability of the available studies, especially as only very few studies
provide non-athletic persons or recreational athletes as a control group [31]
[41]
[42]. Moreover, no
systematic data for older athletes (>30 years) are available. Thus, the
possible long-term consequences of competitive sports on the periodontal
conditions remain unclear. Further studies in representative samples of
different ages should consider different sport types and risk factors in
comparison to a control group. Detailed periodontal examination should include
exact diagnosis, treatment need, and periodontal inflamed surface area to allow
quantification of inflammatory burden.
Impact of oral inflammation on general health
Gingival inflammation is marked by only a small area and the extent of
inflammation. Therefore, an impact on general health is not expected.
Nevertheless, increased values of C-reactive protein (CRP) have been detected in
experimental gingivitis [43].
However, periodontal inflammation is known to be involved in numerous systemic
diseases. The extent of inflammation, i. e., the resulting inflamed
area, seems to presuppose the extent of the effect [44]. The interrelation appears complex and
is explained by a combination of different mechanisms of direct and/or
indirect causality. On the one hand, the chronic bacterial load in in presence
of inflamed tissue with impaired integrity and permeability (here, the
periodontium) can result in recurring bacteremia and thus have a direct
bacterial impact. On the other hand, systemic inflammatory reactions can be
caused by inflammation mediators that are released in the periodontium and
distributed via the blood. Further biological mechanisms are cross-reactions
caused by bacterial or inflammatory dysregulations of the immune defense with
resulting autoaggression, and the swallowing and aspiration of bacteria [45]
[46] are further biological mechanisms. Some studies found respective
differences in blood parameters for patients with periodontitis, while others
did not [47]
[48]. However, changes in circulating blood
cell profiles [32] and increasing CRP
values [49] are reported by recent
systematic reviews and seem to reflect the systemic inflammatory reaction.
Furthermore, periodontal treatment leading to a reduction of the oral
inflammation results also in improvement of these systemic effects [50]
[51]. Additionally, the interrelation between periodontal inflammation
and numerous general diseases is still under discussion [52].
However, due to common factors of predisposition (e. g., smoking,
obesity, genetic predisposition), the causality remains difficult to prove. Such
systemic influences are also discussed for apical periodontal diseases regarding
both systemic diseases [53] and several
blood parameters such as CRP, interleukin (IL-) 1, 2, 6, and immunoglobulin (Ig)
A, G, and M [54]
[55].
Impact of oral inflammation on performance ([Fig. 3])
Fig. 3 The complex network of possible mechanisms of a
bidirectional interaction of competitive sports and oral
inflammation
Limitations and reduced quality of life due to (acute) oral
discomfort
A loss of performance and efficiency is most obvious in cases with acute pain
due to oral health conditions. These are relatively common: 17%
[6] to 30% [29] of athletes in various sports
report pain in the oral region. A total of 4% [5] to 8% [29] declared that they suffered from
acute discomfort at the time of evaluation. Three percent of all athletes in
the 2004 Olympic Games visited the dental clinic in the Olympic Village
[38]. An equally frequent impact
on performance was documented: 3% [3] to 4% [29] of
athletes reported reduced training, and 9% reported difficulties
participating in regular training or competitions [29]. In general, 7% to
18% of the interviewed athletes believed that their oral health
conditions had a negative influence on their training or their performance
over the last 3 and 12 months, respectively [3]
[5]
[29]
[30]. More than 40% of elite athletes feel a generally
negative impact on sports caused by their oral health situation [5]
[30], whereas 20% to 50% also report a negative
impact on their daily life [3]
[5]
[29]
[30]. Thirty-five
percent reported limitations in food intake, 15% in relaxation, and
17% in smiling [29]. This
negative influence on the regeneration and psychosocial well-being of
athletes could indeed reduce their performance, even if they do not seem to
be aware of this context.
For interpreting these data, several points should be considered. First, all
reports from the dental clinic in the Olympic Village [5] have a high selection bias as the
included athletes sought dental treatment. In general, the available data
were not part of routine diagnostic service but a voluntary additional
service [3]
[6]
[29]
[30]. Consequently,
there is also a possible selection bias as the participants could have had
both a higher level of oral health consciousness in general or of dental
complaints. This applies particularly for a small sample [6] and a low response rate [3]. In contrast, Needleman 2016 [30] and Gallagher 2018 [29] could achieve representative
samples of elite athletes in the United Kingdom of eleven sports. Regarding
the impact on quality of life and performance, all data are based on
retrospective self-reported impressions. Furthermore, no data of control
groups are available for comparison.
For future research, longitudinal studies in representative samples should
investigate oral discomforts and resulting restrictions in daily activity in
comparison to non-athletic controls.
Systemic influence on performance.
In this context, a negative influence of periodontitis on performance has
been documented [2]. The increased
extent of periodontal findings (parameters such as PPD, attachment loss, and
bleeding on probing) is related to reduced physical fitness (manual force
and fitness score, respectively) [56]
[57]. Moreover,
periodontal disease severity [58] as
well as increased PPD values (PSI code 3 or 4) [59], were inversely associated with the
maximum oxygen intake capacity (VO2max) as a degree of
cardiovascular fitness, whereas another study did not confirm these findings
[60]. To date, this connection
with physical fitness has not been confirmed for other types of oral
inflammation. However, it is at least assumed for multiple apical sources of
infection [56]. The methodological
quality of these studies was high including clear reporting of the study
settings, reliable measurement of the periodontal conditions by meaningful
parameters and standardized physical fitness tests. In part, the evaluations
were part of large population-based studies with over a thousand
participants [57]
[59]
[60]. Furthermore, potential confounders as age, body mass index
(BMI), smoking, and frequency of exercise were considered [56]
[57]
[58]
[59]
[60].
In competitive athletes, the influence of oral inflammation on performance
has not yet been examined. According to the above-mentioned findings, a
negative impact on performance for athletes experiencing periodontitis would
be expected, at least in cases with severe findings. However,
transferability of the data reported above on elite athletes is limited: The
cohorts had mainly a higher mean age than the cohorts of young elite
athletes that were examined to date. Furthermore, some of the participants
explicitly had a sedentary lifestyle. Furthermore, the revealed differences
refer to a higher extent of periodontal inflammation [56]
[57]
[58]
[59]. In contrast, in athletes mainly
gingivitis and or initial stages of periodontitis were reported ([Table 2]). Interestingly, the one
study that could not reveal differences in cardiorespiratory fitness between
the groups with different periodontal inflammation had low mean PPD and
attachment loss and resulting small group differences of periodontal
inflammation [60]. Nevertheless, it
must be considered that VO2max was only estimated based on heart
rate during exercise. Potentially, in well trained athletes and measured by
spiroergometry small differences in periodontal inflammation could also show
an effect. Therefore, studies in athletes of various age groups with a
detailed periodontal examination should investigate the influence of oral
inflammation (periodontal, gingival, periapical) on performance. Performance
should be measured by a standardized physical fitness test including
VO2max by spiroergometry or strength tests adapted to the
respective disciplines. The periodontal inflammation burden could be
quantified by periodontal inflamed surface area.
Increased risk of muscle injuries
Another potential correlation was described between oral health and muscle
injuries in soccer players. One study showed a (weak) correlation between
increased PPD, plaque index, and muscle injuries [6]. This is especially interesting as
the injuries were documented by the team physician during a one-year
follow-up, and oral health status was assessed clinically. However,
periodontal evaluation was only based on some index teeth. No periodontitis
was reported, hence the detailed periodontal status remains unclear. A
further study documented more non-traumatic muscle and joint injuries in
athletes with periodontitis (according to a detailed full-mouth periodontal
evaluation). However, this effect was not significant in this cohort with
mostly mild periodontal disease severity regarding self-reported injuries
[4]. Nevertheless, it must be
taken in account that the lack of statistical significance could also be
caused by the small cohort size (22 participants). Furthermore, two surveys
indicated poor oral health as a risk factor for injuries [61], respectively reinjuries [62]. However, these surveys were only
based on the self-reported status by the athletes [61]
[62]. It remains unclear if the self-reported surrogate marker
“gum problems (bleeding, swelling, recession)” reflects the
oral inflammation burden in athletes. In particular, gum problems were cited
in one survey as well as not removed wisdom teeth [62]. Even though third molars are a
risk factor in periodontitis, their presence does not indicate periodontal
inflammation in general.
In this context, an increased risk of soft tissue injuries and muscle protein
damage in cases with increased circulating inflammatory cytokines was
observed [63]
[64]. An increase of these cytokines is
also discussed in the context of periodontitis requiring treatment [47].
All in all, a potential increased risk of muscle injuries in case of
increased oral inflammation is an interesting point in sports medicine. A
detailed periodontal examination including the periodontal inflammation
surface area would allow quantification of inflammatory burden. Injuries
should be assessed longitudinally over at least one season.
Possible causes of increased oral inflammation in athletes
There are many possible causes for an increased presence of inflammatory oral
diseases in (competitive) athletes ([Fig.
3]). On the one hand, modified oral health behavior and physical
stress have a strong impact, which will be discussed here. Moreover, the
very time-consuming activity [3],
increased stress [41], physical
constitution [41], nutrition (mainly
so-called “sports nutrition” consumed during training, such
as carbohydrate gels and bars) [39]
[41], and repeated
episodes of dry mouth (due to mouth breathing and fluid loss during
training) play a role. In this context, important individual- and
sports-specific differences occur. Moreover, complex interactions such as
common risk factors must be considered. For example, psychosocial stress is
described as a promoting factor both for gingival inflammation [65]
[66] and staleness [67].
Oral health behavior
Insufficient oral health behavior is a common reason for increased oral
inflammation [68]. Respective
deficiencies were documented, especially for elite athletes ([Table 3]). Regular dental maintenance
appointments [3]
[6]
[30]
[41] and individual oral
hygiene are frequently insufficient, e. g., regarding interdental
care and fluoride supply [31]
[39]. In addition, a dependency on the
duration of training was noted: 97% of the athletes who train up to
20 hours per week brush their teeth twice a day. If training exceeds 20
hours per week, the number drops to 77% [3]. Furthermore, known differences
between competitive and amateur sports [42] and between different teams [30] suggest an influence of coaches and advisors. Again,
available data must be interpreted with caution due to limited comparability
and transferability. The different disciplines [39] and the country of investigation
and socioeconomic status might be influence factors.
Table 3 Oral health behavior of elite
athletes.
|
Oral health behavior
|
Prevalence
|
Cohort
|
References
|
|
Dental appointments in the last year
|
21–81%
|
Professional soccer players, treated athletes in the
Olympic dental clinic 2012, professional rugby players,
Dutch candidates for the Olympic Games 2016
|
Gay-Escoda et al. 2011 [6], Needleman et al. 2013 [5], Minty et al.
2018 [41], Kragt
et al. 2019 [3]
|
|
Tooth brushing (daily)
|
100%
|
Elite triathletes, Dutch candidates for the Olympic Games
2016, endurance athletes from German perspective, and
youth squads
|
Bryant et al. 2011 [101], Kragt et al. 2019 [3], Merle et al.
2022 [31]
|
|
Tooth brushing (at least twice daily)
|
60–94%
|
Elite triathletes, professional soccer players, elite
athletes in Great Britain, Dutch candidates for the
Olympic Games 2016
|
Bryant et al. 2011 [101], Gay-Escoda et al. 2011 [6], Gallagher et
al. 2019 [39],
Kragt et al. 2019 [3]
|
|
Interdental care
|
44%
|
Elite athletes in Great Britain, endurance athletes from
German perspective, and youth squads
|
Gallagher et al. 2019 [39], Merle et al. 2022 [31]
|
|
Use of fluoride mouthwash
|
41–49%
|
Elite athletes in Great Britain
|
Gallagher et al. 2019 [39]
|
|
Use of fluoride gels
|
11%
|
Endurance athletes from German perspective, and youth
squads
|
Merle et al. 2022 [31]
|
Influence of physical activity on inflammation
Physical stress influences the inflammation load. Generally, regular physical
activities are described as promoting health: Physical activity leads to
fewer proinflammatory cytokines in the blood and therefore has a positive
influence on numerous diseases [69]
[70]. Regarding oral
inflammation, physically active subjects report less gingival bleeding and
tooth mobility than physically inactive subjects [71]. Actually periodontitis is less
diagnosed in physically active subjects, especially those who perform 3 to 5
training units per week [72]. Here,
the reduction of the immunomarkers CRP and IL-1ß, which are
increased in numerous diseases, including periodontitis, seems to play a
role [73]. While regular moderate
physical activities have a positive influence on oral health, this effect
cannot be completely transferred to elite sports. Training stimuli activate
inflammatory-like processes: Up to 72 hours after loading, systemic
(pro-inflammatory) markers such as CRP, IL-1β, IL-6, IL-8, IL-10,
and tumor necrosis factor alpha (TNF-α) [74]
[75]
[76] as well as the
stress hormones cortisol and adrenaline [77] increase significantly in the blood, while immunoglobulin A
in the saliva decreases [78]. As these
(pro-)inflammatory markers circulate in the blood, are expressed in saliva
and play a pathogenic role in oral inflammatory processes [79]
[80], they could affect the oral tissues. Nevertheless, changes in
interleukins depend on extend of physical activity and were described
especially for long-distance running [74]
[76]. Furthermore, the
causality of elevated periodontal destruction due to elevated systemic
inflammation has not been proven despite various assumptions in the
interrelationship of systemic conditions and periodontitis [81]
[82]. In addition, cellular defense is temporarily reduced [83]. This could favor infections after
intensive physical exercise (“open window theory”) [84]
[85]. How far these factors influence oral health in athletes has
not yet been evaluated.
In the same way, elevated cortisol, and catecholamine values due to physical
activity could play a role: Increased values have been detected in patients
with periodontitis [86]. However, many
confounders could have led to a meaningful bias [86]. Furthermore, catecholamines
promote the expression of virulence factors in periodontopathogenic bacteria
such as Porphyromonas gingivalis
[87].
Such mechanisms should also be discussed for the potential connection between
oral health and muscle injuries: Among others, creatine kinase and IL-6 are
released due to exercise [75] and are
reported to negatively influence periodontal disease burden [88]. Even tough sex, age, and smoking
behaviors were consideres as confounders, the results of this singular study
must be interpreted with caution: Further factors such as muscular injuries
and resulting stress might have an influence.
Prospective studies with measurement of both systemic parameters such as
interleukins and oral inflammation before and after physical exercise should
be conducted.
Implementation of dental care in (elite) athletes
The increased risk for oral diseases and their possibly severe consequences in
the individual athlete demonstrate the relevance of adequate dental care in
professional sports.
Protecting the health of athletes is one priority of the international sports
federations [89]. Therefore, both the
International Olympic Committee (IOC) and the Union of European Football
Associations (UEFA) have explicitly included oral health in their statements
[90]
[91] and recommend regular dental examinations [90].
Key issues are comprehensive examination, education, appropriate treatment, and
prevention. The first point requires regular dental screenings. Consequently,
annual dental examinations for example as part of the regular preseason sports
medical check [92]
[93]
[94], and for elite athletes, a second dental check-up per year [93] is recommended. To this end, uniform
examination criteria are demanded [92].
The World Dental Federation (FDI) recommends including dental status (DMFT index
and erosion), periodontal condition (PPD, plaque, and gingival index), dental
occlusion, the temporomandibular joint, saliva, facial muscles, third molars,
nutritional habits, inflammation, and medical history. Indication-based
radiologic examinations or other further investigations can be conducted [93]. In particular, examination directly at
the training venue is well accepted by the athletes [92].
Besides screening and individual treatment, risk- and individual-based strategies
for prevention are essential [95].
Particularly, education of athletes on sports-related risk factors, motivation,
and instruction for individual oral hygiene should be included. The increasing
interest of athletes and coaches indicates potential: More than 80% of
athletes stated being willing to change certain behaviors to improve their oral
health [39]. Actually a prevention
strategy combining general and personalized advice could improve both knowledge
and oral health behavior of athletes [96].
This proves the effectiveness of such measures. However, repetition seems
necessary to maintain the effects, e. g., regarding gingival
inflammation [96]. Short (10 min)
educational interventions are well accepted and implementable in
high-performance sports [96]. Furthermore,
the athletes’ team of coaches and trainers should also receive
structured information for improving oral health in sports. Standard
recommendations for individual oral hygiene include toothbrushing with fluoride
toothpaste at least twice a day for two minutes, flosses/interdental
brushes, and rinsing with water, or chewing sugar-free gum after meals and
snacks when brushing is not possible [97].
Overall, establishing a specially trained “team dentist” or
sports dentist” is reasonable [92]
[94]
[98]. These experts would be able to provide
sport-specific advice in close coordination with the athlete’s support
team [92]. So, special prevention
strategies such as the application of protective substances inside of
mouthguards [99] could be established by
these experts. This could be the setting for an adequate interdisciplinary
sports dental care concept. In addition, this would also facilitate the work of
general dentists by providing a link to the support team of the athletes.
Furthermore, such integration of sports dentistry into sports medicine would
improve research in this field [94].