CC BY-NC-ND 4.0 · Sports Med Int Open 2019; 03(01): E25-E31
DOI: 10.1055/a-0891-7021
Training & Testing
Eigentümer und Copyright ©Georg Thieme Verlag KG 2018

Influence of Mouthguards on Physiological Responses in Rugby

Antina Schulze
1   Universität Leipzig, Institute of Sports Medicine, Leipzig, Germany
,
Stefan Kwast
1   Universität Leipzig, Institute of Sports Medicine, Leipzig, Germany
,
Martin Busse
2   Universität Leipzig, Institut für Sportmedizin & Prävention, Leipzig, Germany
› Author Affiliations
Further Information

Correspondence

Dr. Antina Schulze, DDS
Universität Leipzig, Institute of Sports Medicine,
Marschnerstr. 29,
04109 Leipzig
Germany   
Phone: +49/341/9731 741   
Fax: +49/341/9731 748   

Publication History

received 03 January 2019
revised 18 March 2019

accepted 08 April 2019

Publication Date:
05 June 2019 (online)

 

Abstract

Mouthguards (MGs) are highly recommended in rugby. Airway obstruction and a resulting decrease in power output are potential disadvantages of their usage. The aim of the study was to assess possible limitations of “vented” (MGV) and custom-made mouthguards (MGC) on rugby players’ performance. The MG effects were investigated in 13 male first-league rugby players ranging from 18–34 years old. First a lung function test was completed. Then a double incremental treadmill test was performed to measure maximum aerobic performance, ventilation, VO2, VCO2, heart rate, and lactate. Effects on sprint times (10 and 40 m) and countermovement jumps were also investigated. Peak flow values were significantly decreased with MGV by about 0.9 l/s. Neither ventilatory parameters nor oxygen uptake were affected by either of the mouthguards. Maximum lactate was significantly decreased in both MG types vs. no MG use. The maximum running velocity was similar in all tests. The aerobic energy turnover was moderately increased with the MGC and MGV. No effects were seen on sprint times or jump tests. Although neither type of mouthguard had a significant impact on maximum performance in treadmill running, the anaerobic energy turnover was decreased.


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Introduction

Considering the risk of dental trauma in contact sports, mouthguards are an essential piece of safety gear for athletes to soften impacts and prevent injuries [1] [26] [27]. The American Dental Association recommends the use of MGs in 29 sports [5]. The Fédération Dentaire International [14] subdivides organized sports into two categories based on the risk of traumatic dental injuries: high-risk sports (such as American football, hockey, ice hockey, lacrosse, martial arts, rugby, inline skating, skateboarding and mountain biking) and medium-risk sports (such as basketball, soccer, handball, squash, gymnastics, parachuting and water polo). Use of an MG is mandatory for rugby players. Nevertheless, 12–37% of rugby players do not use an MG during training or competition [8] [23] [24] [28] [31]. The major concern is a possible decrease in performance and increase in breathing resistance.

A custom-made MG (MGC) is characterized by a better fit and comfort when compared to a boil-and-bite MG [6] [35]. However due to lower costs, often boil-and-bite MGs are used [25] [29]. Many players do not use an MG because they expect negative respiratory effects. Recently, an MG with breathing channels was developed (Nike Adult Max Intake, Beaverton, OR, USA). Studies on this type of MG (MGV) have been performed by Bailey et al. [5] (recreationally trained males using a cycle ergometer) and Schulze et al. [32] (basketball specific tests). In these settings ventilation and blood lactate were significantly decreased with MGV.

The results for oxygen uptake and ventilation at maximum and sub-maximum load for MGC are inconsistent: five studies reported no differences in either respiratory or cardiac parameters with the MGC [6] [9] [25] [30] [35]. Garner et al. [17] found significantly higher oxygen uptake and ventilation in constant-load exercise. Two studies showed a significantly improved cycle ergometer performance with an MGC [[30] [35]. However, no significant differences were found in running performance with an MGC [[6] [9] [25].

Important elements in rugby are sprint performance and explosive strength. The use of a mouthguard may have positive effects on neuromuscular chains. A mouthguard may facilitate powerful jaw clenching and a subsequent concurrent activation potentiation through a remote voluntary contraction of the mandible muscles [2] [7] [12]. Remote voluntary contractions are a muscle action of the prime mover while performing a simultaneous muscle action with another part of the body [12].

A common disadvantage of all the above-mentioned studies was that the athletes were not accustomed to MG use. The current study is new in three aspects: 1. The subjects were highly trained first-league rugby players who used mouthguards regularly. 2. Typical sports-specific elements were used in a laboratory setting (double incremental treadmill tests, sprints and countermovement jumps) to investigate the mouthguard effects on oxygen uptake, ventilation and blood lactate. 3. Two mouthguard types were compared to no mouthguard use: custom-made mouthguards with an advantage of proper fit, and vented mouthguards with an advantage of specific breathing channels. For coaches and athletes, the study aimed to determine whether a mouthguard with a specific design for improved ventilation would have better physiological responses in comparison to a custom-made mouthguard with a known high level in comfort and protection.


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Materials and Methods

Subjects

The study was approved by the Institutional Review Board and Human Medical Research Committee at the University of Leipzig, Germany (No. 445–15–21122015). Written informed consent was obtained from all participants after they confirmed complete understanding of the study protocol. The study conformed to the Standards for Ethics in Sport and Exercise Science Research [22] and required players to provide informed consent before participation. Participants included 13 male subjects between 18 and 34 years old (mean 24.7±4.9 years, height=184.6±5.7 cm, weight=89.25±12.8 kg, BMI=26.25±3 kg/m2) who played in the first German rugby league and had a middle position in the league ranking. Exclusion criteria were: acute/chronic infections, antibiotic therapy, chronic/systemic diseases, joint problems, and injuries. In total, 16 players were measured. After 3 dropouts due to sickness or incomplete data acquisition, 13 players were included.


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Mouthguards

The subjects were told that two different kinds of mouthguards would be tested. No information was given about possible advantages or disadvantages in comparison to their personal mouthguards. Two types of mouthguards were used: the vented boil-and-bite mouthguard (MGV, Nike, Beaverton, OR, USA) and the custom-made mouthguard. The MGV has patented breathing channels (O-FlowTM) designed to improve the ventilation and oxygen uptake during athletic activity ([Fig. 1]). Compared to traditional mouthguards, these additional air inlets are designed to allow less restricted breathing. The MGV was placed in boiling water for 30 s and was then carefully placed in the subject’s mouth to cover their upper teeth. The subject was instructed to bite down firmly. Moderate pressure was placed on the lips and cheeks for 30 s. The MGV was then removed and rinsed in cold water.

Zoom Image
Fig. 1 Vented mouthguard used in this study (MGV).

The custom-made mouthguard (MGC) was vacuum-formed over a stone model that had been prepared from the dental impression (alginate) and a bite registration to adjust an occlusal equilibration ([Fig. 2]). The thermoforming plate had a thickness of 5 mm (Bioplast Xtreme, Scheu Dental, Iserlohn, Germany).

Zoom Image
Fig. 2 Custom-made mouthguard used in this study (MGC).

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Lung function measurements

Prior to the exercise tests, a lung function measurement at rest was performed using a tube (Easy on-PC, NDD, Zürich, Schweiz). Vital capacity (VC), forced vital capacity (FVC), peak flow (PEF), and forced 1-second expiratory volume (FEV1) were displayed.


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Treadmill protocol

The subjects performed two subsequent treadmill tests with a 5-minute rest in between (double incremental treadmill exercise, Test A and Test B). In Test A, all spiroergometric data were measured. Test B was used to measure the individual lactate equilibrium (lactate minimum test [34]). In Test A, no lactate samples were taken because the stops for blood sampling would have disturbed the spiroergometric measurements. The treadmill was adjusted to an incline of 1%. Test A began with a 4-minute warm-up (2 min at 6 km/h and 2 min at 8 km/h). Then the load was increased by 1 km/h each minute until exhaustion to produce near-to-ramp increments. During the 5 min recovery, a speed of 6 km/h was maintained. Lactate samples (20 µl) were taken at rest from the hyperaemized ear lobe immediately after Test A and after the first, third, and fifth minute of the break. This break allowed for lactate distribution in the intra- und extracellular space.

In Test B, the running speed was increased by the usual increments of 2 km/h every 2 min until exhaustion. A 5-min. recovery at 6 km/h followed. Lactate was taken after each speed step (at which point the subjects stood on the side bars for 15 s) and after the first, third, and fifth minute of the break. The treadmill tests (n=39) were performed in a randomized order using either no MG, the MGV or MGC in the Sports Medicine laboratory at the University of Leipzig.


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Exercise testing

Heart rate (HR), oxygen uptake (VO2), ventilation (VE), tidal volume (VT), breathing rate (BR), and carbon dioxide output (VCO2) were measured. The spiroergometric data was measured breath-by-breath with a mask (K4b2, Cosmed, Italy). The VO2 and VCO2 values were calculated from the end-expiratory gas concentrations and VE. VE was calculated as the product of BR and VT. HR was taken from the continuous ECG recording. Super GL (ISO 7550, Germany) was used for the blood lactate measurement.


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Sprint and jump protocol

Sprint and jump tests are performance markers for team sport athletes. Ten- and forty-meter sprint tests were used to determine acceleration, maximum speed, and anaerobic performance. Countermovement jumps (CMJ) were performed to measure explosive lower-body power performance and explosive strength. Sprint and countermovement tests are generally used by strength and conditioning coaches as differential measurements of speed and strength. For the measurement of sprints and jumps, SmarTrack Diagnostics from Humotion (Münster, Germany) was used. This mobile measuring system consists of a hip belt with an integrated electronic unit. The performance was measured by two modules. The jump module independently detects and records three different jump modes: squat jump (SJ), countermovement jump (CMJ) and drop jump (DJ). The sprint module records the exact running times in the linear sprint. The length of the sprints can be varied by mobile magnetic barriers. A complex sensor system was used to collect the data. The acceleration in all three directions is registered by an acceleration sensor, which also detects the static acceleration due to gravity. The measurement of the movement is performed by a 3-D magnetic field sensor. The speed of the body movement is registered in all three directions via rotational speed sensors. The interaction of all sensors makes it possible to follow the movements of the body or individual body segments.

Prior to the tests, the subjects took part in a standardized warm-up. For the sprint tests the subjects started 1 m before the starting line. After the last sprint, the jump force was measured after a 2 min break. Three consecutive countermovement jumps were then performed with a 1 min break between the jumps. The athletes performed the tests in a randomized order with the MGV, MGC, and NoMG. Before testing, the subjects had practice sessions to train for the countermovement jumps.

In all anaerobic tests, the subjects were advised to bite on the MG to ensure an occlusal position [21], but no breathing instructions were given.


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Statistical analysis

Results are expressed as the means±SD. Data for all variables were tested for and found to be normally distributed using the Shapiro-Wilk test. A repeated-measures ANOVA design was used to assess the statistical significance of differences between the mean values of the different conditions. To confirm differences between groups, Tukey’s post hoc test was used. A p-value<0.05 was considered significant and a p-value<0.005 was considered highly significant. Also, the 95% confidence interval (CI) was calculated. All analyses were performed using the GraphPadInStat Software (GraphPadSoftware, La Jolla, CA, USA) and the IBM Statistics package software, version 22.0 (IBM SPSS Statistics, Armonk, NY, USA).


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Results

Lung function results

Peak flow was significantly decreased with MGV vs. NoMG or MGC. No mouthguard effects on other lung function parameters were seen ([Table 1]).

Table 1 Lung function results (SD in brackets).

NoMG

MGV

MGC

p-value

VC (l)

5.52 (0.62)

5.50 (0.82)

5.40 (0.80)

n.s.

FVC (l)

5.43 (0.63)

5.37 (0.69)

5.32 (0.61)

n.s.

FEV1 (l)

4.91 (0.64)

4.80 (0.63)

4.80 (0.63)

n.s.

Peak flow (l×s −1)

10.90 (1.84)

9.99 (1.63)*

10.60 (1.66)

0.002 (NoMG vs. MGV)
0.04 (MGV vs. MGC)

FEF 25–75% of FVC (l×s −1)

5.82 (1.43)

5.64 (1.27)

5.86 (1.66)

n.s.


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Treadmill testing results

Compared to NoMG use, the oxygen uptake was moderately, however insignificantly, higher with the MGC at submaximal and maximum load ([Table 2]). Maximum lactate values were lower when using a mouthguard (MGV: p<0.002; MGC: p<0.04).

Table 2 Exercise results.

Parameter

Intensity

NoMG

MGV

MGC

p-value

VO 2 (ml×min −1 )

sub

4461 (533)

4589 (570)

4697 (530)

n.s.

(4139–4783)

(4245–4934)

(4376–5017)

max

4541 (575)

4608 (612)

4747 (598)

n.s.

(4193–4888)

(4238–4978)

(4386–5108)

VCO 2 (l×min −1 )

sub

4895 (626)

5042 (611)

5045 (491)

n.s.

(4517–5272)

(4673–5411)

(4748–5342)

max

5131 (640)

5131 (690)

5159 (646)

n.s.

(4745–5518)

(4714–5548)

(4769–5549)

HR (bpm)

sub

183.8 (7.8)

183.4 (6.6)

182.0 (5.9)

n.s.

(178.8–188.8)

(179.2–187.6)

(178.2–185.7)

max

184.4 (5.9)

183.7 (5.7)

182.6 (6.1)

n.s.

(180.6–188.1)

(180.1–187.3)

(178.7–186.4)

VE (l×min −1 )

sub

135.2 (17.2)

135.6 (16.4)

137.3 (21.1)

n.s.

(124.8–145.6)

(125.7–145.5)

128.0–146.6)

max

143.8 (16.7)

139.5 (18.4)

142.6 (23.7)

n.s.

(133.7–153.9)

(128.4–150.6)

(128.0–146.6)

BR (breath×min −1 )

sub

47.6 (8.2)

46.9 (6.3)

47.6 (5.0)

n.s.

(42.6–52.5)

(43.1–50.7)

(44.5–50.7)

max

50.7 (6.1)

47.9 (4.7)

49.1 (5.9)

n.s.

(47.0–54.3)

(45.1–50.8)

(44.5–50.7)

VT (l)

sub

2.92 (0.57)

2.95 (0.53)

2.92 (0.48)

n.s.

(2.58–3.26)

(2.63–3.27)

(2.63–3.21)

max

2.90 (0.54)

2.95 (0.49)

2.94 (0.51)

n.s

(2.57–3.22)

(2.65–3.24)

(2.63–3.25)

RQ

sub

1.10 (0.10)

1.10 (0.10)

1.08 (0.07)

n.s.

(1.04–1.16)

(1.05–1.16)

(1.04–1.12)

max

1.13 (0.08)

1.12 (0.10)

1.09 (0.09)

n.s.

(1.08–1.18)

(1.06–1.18)

(1.05–1.13)

FeO 2 (vol%)

sub

15.64 (0.61)

15.57 (0.39)

15.63 (0.48)

n.s.

(15.27–16.01)

(15.34–15.81)

(15.34–15.92)

max

15.84 (0.49)

15.57 (0.32)

15.65 (0.50)

n.s.

(15.54–16.13)

(15.37–15.76)

(15.36–15.94)

FeCO 2 (vol%)

sub

5.91 (0.73)

6.00 (0.69)

5.89 (0.60)

n.s.

(5.48–6.35)

(5.57–6.40)

(5.53–6.25)

max

5.85 (0.62)

5.85 (0.81)

5.89 (0.588)

n.s.

(5.47–6.22)

(5.36–6.35)

(5.53–6.24)

Inspiratory time (s)

sub

0.63 (0.10)

0.64 (0.08)

0.61 (0.08)

n.s.

(0.57–0.69)

(0.59–0.69)

(0.56–0.66)

max

0.58 (0.07)

0.62 (0.06)

0.60 (0.08)

n.s.

(0.54–0.62)

(0.58–0.66)

(0.56–0.65)

Expiratory time (s)

sub

0.67 (013)

0.67 (0.11)

0.65 (0.11)

n.s.

(0.59–0.76)

(0.60–0.73)

(0.58–0.71)

max

0.62 (0.10)

0.65 (0.08)

0.64 (0.10)

n.s.

(0.56–0.68)

(0.60–0.70)

(0.58–0.70)

Velocity (km×h −1 )

sub

15.08 (1.32)

max

15.54 (1.05)

15.38 (1.39)

15.23 (1.36)

n.s.

(14.90–16.17)

(14.55–16.22)

(14.41–16.05)

Blood lactate (mmol×l −1 )

pre

0.85 (0.19)

0.75 (0.14)

0.74 (0.11)

n.s.

(0.73–0.97)

(0.66–0.83)

(0.67–0.81)

max

10.42 (2.27)

8.94 (1.89)*

9.42 (2.39)*

0.002 (NoMG vs. MGV)

(9.06–11.79)

(7.82–10.06)

(7.98–10.86)

0.04 (NoMG vs. MGC)

AT lac (km×h −1 )

10.6 (1.5)

10.6 (1.5)

10.9 (1.0)

n.s.

(9.71–11.52)

(9.71–11.52)

(10.3–11.55)

Mean value (SD) and confidence interval in brackets. Maximum values (max): mean values corresponding to the highest speed in each test series (NoMG, MGV, MGC). Submaximum values (sub): mean values corresponding to the series (NoMG, MGV, MGC) with the lowest maximum speed. Pre: pre-exercise values. ATlac (anaerobic lactate threshold): running speed corresponding to the lactate minimum (18) in Test B. * = significant.

The relation between VO2 and lactate values in all test conditions was significantly higher with the MGs ([Table 3]).

Table 3 Metabolic rate in the tests due to the use of mouthguards (SD in brackets).

Aerobic kcal×min−1

Anaerobic kcal×min−1

Total kcal×min−1

Aerobic/anaerobic Quotient

NoMG

184.9 (28.07)

12.99 (3.32)

17.25 (1.81)

15.00 (3.60)

MG V

178.2 (27.29)

11.11 (2.57)

17.27 (1.75)

16.68 (3.11)

p<0.001

p<0.02

MG C

185.6 (34.54)

11.78 (3.74)

17.83 (2.45)

16.63 (3.70)

p<0.04

p<0.03

P-values refer to the differences between NoMG and MGV or MGC.


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Sprint and jump results

The results for the sprints and vertical jumps were almost identical. However, there was a tendency for better sprint times with an MG ([Table 4]).

Table 4 Sprint and vertical jump results.

Test

NoMG

MGV

MGC

p-value

40 m sprint (s)

mean

5.44 (0.3)

5.42 (0.3)

5.42 (0.3)

n.s.

(5.26–5.62)

(5.22–5.62)

(5.24–5.60)

best

5.39 (0.3)

5.37 (0.4)

5.36 (0.4)

n.s.

(5.21–5.57)

(5.16–5.58)

(5.15–5.56)

10 m sprint (s)

mean

1.58 (0.1)

1.57 (0.1)

1.58 (0.1)

n.s.

(1.53–1.63)

(1.53–1.61)

(1.54–1.62)

best

1.57 (0.1)

1.56 (0.1)

1.56 (0.1)

n.s.

(1.52–1.61)

(1.51–1.60)

(1.52–1.60)

Jump height (cm)

mean

41.3 (7.5)

41.9 (6.4)

41.5 (7.4)

n.s.

(36.8–45.9)

(38.0–45.75)

(37.0–46.0)

best

43.9 (7.7)

44.6 (6.7)

44.0 (7.6)

n.s.

(39.4–48.4)

(40.7–48.4)

(39.6–48.3)

Means (SD) and confidence interval in brackets.


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Discussion

Lung function

In the current study, only the peak flow was significantly lower with MGV vs. NoMG or MGC. No further significant differences in lung function were seen, which is in line with other studies [6] [10]. However, these conditions do not reflect the game situation because the jaw was fixed in the tests by biting on the mouth tube. When a mask is used instead of a mouth tube, the airflow may be affected even less [3]. The increased inspiratory resistance at rest may be reduced in hyperpnea conditions [3]. The expiratory airflow can also be affected by the MG thickness and the position of the head, neck and jaw [3]. According to Amis et al. [3], the natural flow pattern of the oral cavity may even be positively influenced by the MGC so that the airflow becomes less turbulent. All these aspects must be considered as a possible cause for the differences between the two MGs regarding expiratory flow and maximum exercise ventilation.


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Aerobic and metabolic responses

In the current study, the maximum blood lactate was significantly lower with MG use (approximately 10% for MGV and 4% for MGC, respectively). The blood lactate values are dependent on the anaerobic metabolism and muscle glycogen stores [34]. The tests were performed in a randomized order and instructions for nutrition goals were given to refill the glycogen stores. Therefore, different glycogen stores were not expected.

The maximum running speed was almost equal in all tests and there was a tendency toward even higher VO2 values with MG. Theoretically this might indicate slightly reduced energy conversion efficiency. However, lower blood lactate together with a slightly increased VO2 more likely indicates an improved aerobic metabolism due to the MG.

Lower lactate concentrations with MG were also found in other studies [5] [16] [18] [32]. Garner and McDivitt [16] hypothesized that an increase in the respiration diameter and a resulting increase in CO2 elimination might explain the lower lactate values with MG use. This cannot be confirmed by the current or former results [32], where no differences in CO2 output were measured at maximum load. Bailey et al. [5] found significantly lower lactate concentrations at submaximal and maximum load with the MGV. They assumed that the aerobic energy production might have been improved in the MGV condition. A possible explanation has been given by Francis and Brasher [15]. They hypothesized that the MG might cause a “pursed-lip” type of breathing, which has been shown to decrease CO2 tension, and increase oxygenation and exercise tolerance [15]. If this applies, a higher O2 gradient between the alveoli and the lung capillaries might result. This could also explain slightly increased VO2 and decreased blood lactate values as observed in the current study.


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Cardiorespiratory responses

Although the peak flow was lower with the MGV in the current study, maximum VE was similar to NoMG and MGC. This may indicate that the major effect of the MGV cannot be attributed to the air channels but to the use of a mouthguard in principle.

HR and VE were similar in all conditions. With respect to recent studies, the type of exercise (ergometer, treadmill, or sports-specific course) may affect the cardiorespiratory response. In the majority of treadmill tests, ventilation was not affected by MG use [6] [13] [19] [21] [25]. In contrast, VE was lower with MG in cycle ergometer testing [5] [15]. In a sports-specific environment, VE was lower with MG [32] [33]. No explanations are provided for the differences in cycle ergometer and treadmill testing. In contrast, in a field setting, the body biomechanics may be different because the jaw may act as a second whole body stabilization area together with the core muscles [32]. It is unlikely that this effect plays a role in a laboratory treadmill or cycle ergometer test.


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Sprint and jump results

The sprint time over a short distance is an indicator of anaerobic performance. The sprint time was also used to assess the influence of the MGC/V on anaerobic performance. In the current study, no significant effects were found with both MGs. This is in line with other studies [4] [5] [11] [18] [20].

Although the current study did not show any significant differences in the countermovement jumps, the most frequent peak values were seen under the influence of the MGV. Recent studies reported significant improvements for the CMJ with the MGC [4] [11]. Bailey et al. [5] found higher vertical jump values with the MGV. However, as in the current study, most studies did not reveal any significant differences [10] [11] [20].

The current study is based on treadmill testing, sprints, and countermovement jumps to isolate the specific mouthguard effects. Ventilation was not reduced as seen in handball- and basketball-specific studies [32] [33]. However, there were also no negative effects on breathing or performance during exercise. The laboratory tests did show an ergogenic effect on the aerobic metabolism. Therefore, for future studies a rugby course will be created and evaluated for sports-specific field testing and then compared to the current laboratory test results in a larger cohort for general implications. Furthermore, studies on the longitudinal effects of the different mouthguard types will be of interest.


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Conclusions

Custom-made and vented mouthguards have no negative effects on rugby-specific performance or breathing parameters when tested in a laboratory setting. Maximum exercise capacity, sprints, and jumps are not affected by the use of these two mouthguard types. It is a new observation that aerobic energy turnover may even be improved in rugby-specific motion elements, regardless of whether custom-made or vented mouthguards were used. Presumably, these results can be transferred to authentic game and training situations.


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Conflict of Interest

Authors declare that they have no conflict of interest.

Acknowledgements

We thank Tim Albrecht and Christian Senf for their support in data acquisition.

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  • 8 Chapman PJ. Orofacial injuries and international rugby player’s attitudes to mouthguards. Br J sports Med 1990; 24: 156-158
  • 9 Collares K, Correa MB. Mohnsam da Silva IC, Hallal PC, Demarco FF. Effect of wearing mouthguards on the physical performance of soccer and futsal players: A randomized cross-over study. Dent Traumatol 2014; 30: 55-59
  • 10 Duarte-Pereira DM, Del Rey-Santamaria M, Javierre-Garcés C, Barbany-Cairó J, Paredes-Garcia J, Valmaseda-Castellón E, Berini-Aytés L, Gay-Escoda C. Wearability and physiological effects of custom-fitted vs. self-adapted mouthguards. Dent Traumatol 2008; 24: 439-442
  • 11 Dunn-Lewis C, Luk HY, Comstock BA, Szivak TK, Hooper DR, Kupchak BR, Watts AM, Putney JR, Volek JS, Denegar CR, Kraemer WJ. The effects of a customized over-the-counter mouth guard on neuromuscular force and power production in trained men and women. J Strength Cond Res 2012; 26: 1085-1093
  • 12 Ebben WP, Kaufmann CE, Fauth ML, Petushek EJ. Kinetic analysis of concurrent activation potentiation during back squats and jump squats. J Strength Cond Res 2010; 24: 1515-1519
  • 13 Evans BW, Potteiger JA. Metabolic and ventilatory responses to submaximal and maximal exercise using different breathing assemblies. J Sports Med Phys Fitness 1995; 35: 93-98
  • 14 Fédération Dentaire Internationale (FDI). Commission on dental products. working party No 7: 1990
  • 15 Francis KT, Brasher J. Physiological effects of wearing mouthguards. Br J Sports Med 1991; 25: 227-231
  • 16 Garner DP, McDivitt E. Effects of mouthpiece use on airway openings and lactate levels in healthy college males. Compend Contin Educ Dent 2009; 30: 9-13
  • 17 Garner DP, Dudgeon WD, Scheett TP, McDivitt EJ. The effects of mouthpiece use on gas exchange parameters during steady-state exercise in college-aged men and women. J Am Dent Assoc 2011; 142: 1041-1047
  • 18 Garner DP. Effects of various mouthpieces on respiratory physiology during steady-state exercise in college-aged subjects. Gen Dent 2015; 63: 30-34
  • 19 Gebauer DP, Williamson RA, Wallman KE, Dawson BT. The effect of mouthguard design on respiratory function in athletes. Clin J Sport Med 2011; 21: 95-100
  • 20 Golem DL, Arent SM. Effects of over-the-counter jaw-repositioning mouth guards on dynamic balance, flexibility, agility, strength, and power in college-aged male athletes. J Strength Cond Res 2015; 29: 500-512
  • 21 Golem DL, Davitt PM, Arent SM. The effects of over-the-counter jaw-repositioning mouthguards on aerobic performance. J Sports Phys Fitness 2017; 57: 865-871
  • 22 Harriss DJ, Macsween A, Atkinson G. Standards for ethics in sport and exercise science research: 2018 update. Int J Sports Med 2017; 38: 1126-1131
  • 23 Ilia E, Metcalfe K, Heffernan M. Prevalence of dental trauma and use of mouthguards in rugby union players. Aust Dent J 2014; 59: 473-481
  • 24 Kay EJ, Kakarla P, Macleod DA, McGlashan TP. Oro-facial and dental injuries in club rugby players. Br J Sports Med 1990; 24: 271-273
  • 25 Keçeci AD, Cetin C, Eroglu E, Baydar ML. Do custom-made mouth guards have negative effects on aerobic performance capacity of athletes?. Dent Traumatol 2005; 21: 276-280
  • 26 Knapik JJ, Marshall SW, Lee RB, Darakjy SS, Jones SB, Mitchener TA, delaCruz GG, Jones BH. Mouthguards in sport activities: History, physical properties and injury prevention effectiveness. Sports Med 2007; 37: 117-144
  • 27 Mihalik JP, McCaffrey MA, Rivera EM, Pardini JE, Guskiewicz KM, Collins MW, Lovell MR. Effectiveness of mouthguards in reducing neurocognitive deficits following sports-related cerebral concussions. Dent Traumatol 2007; 23: 14-20
  • 28 Muller-Bolla M, Lupi-Pegurier L, Pedeutour P, Bolla M. Orofacial trauma and rugby in France: epidemiological survey. Dent Traumatol 2003; 19: 183-192
  • 29 Newsome PR, Tran DC, Cooke MS. The role of the mouthguard in the prevention of sports-related dental injuries: a review. Int J Paediatr Dent 2001; 11: 396-404
  • 30 Piero M, Simone U, Jonathan M, Maria S, Giulio G, Francesco T, Gabriella C, Laura A, Eva B, Gianni N, Francesco C, Giovanni G. Influence of a custom-made maxillary mouthguard on gas exchange parameters during incremental exercise in amateur road cyclists. J Strength Cond Res 2015; 29: 672-677
  • 31 Schildknecht S, Krastl G, Kühl S, Filippi A. Dental injury and its prevention in Swiss rugby. Dent Traumatol 2012; 28: 465-469
  • 32 Schulze A, Kwast S, Busse M. Vented mouthguard effects on cardiopulmonary parameters in basketball: A pilot study. EC Dent Sci 2017; 15: 182-190
  • 33 Schulze A, Laessing J, Kwast S, Busse M. Influence of a vented mouthguard on physiological responses in handball. J Strength Cond Res 2018; 23: [Epub ahead of print]
  • 34 Tegtbur U, Busse MW, Braumann KM. Estimation of an individual equilibrium between lactate production and catabolism during exercise. Med Sci Sports Exerc 1993; 25: 620-627
  • 35 Von Arx T, Flury R, Tschan J, Buergin W, Geiser T. Exercise capacity in athletes with mouthguards. Int J sports Med 2008; 29: 435-438

Correspondence

Dr. Antina Schulze, DDS
Universität Leipzig, Institute of Sports Medicine,
Marschnerstr. 29,
04109 Leipzig
Germany   
Phone: +49/341/9731 741   
Fax: +49/341/9731 748   

  • References

  • 1 ADA Council on Access, Prevention and Interprofessional Relations, and ADA Council on Scientific Affairs . Using mouthguards to reduce the incidence and severity of sport-related oral injuries. J Am Dent 2006; 137: 1712-1720
  • 2 Allen CR, Fu YC, Cazas-Moreno V, Valliant MW, Gdovin JR, Williams CC, Garner JC. Effects of jaw clenching and jaw alignment mouthpiece use on force production during vertical jump and isometric clean pull. J Strength Cond Res 2018; 32: 237-243
  • 3 Amis T, Di Somma E, Bacha F, Wheatley J. Influence of intra-oral maxillary sports mouthguards on the airflow dynamics of oral breathing. Med Sci Sports Exerc 2000; 32: 284-290
  • 4 Arent SM, McKenna J, Golem DL. Effects of a neuromuscular dentistry-designed mouthguard on muscular endurance and anaerobic power. Comp Exerc Physiol 2010; 7: 284-290
  • 5 Bailey SP, Willauer TJ, Balilionis G, Wilson LE, Salley JT, Bailey EK, Strickland TL. Effects of an over-the-counter vented mouthguard on cardiorespiratory responses to exercise and physical agility. J Strength Cond Res 2015; 29: 678-684
  • 6 Bourdin M, Brunet-Patru I, Hager PE, Allard Y, Hager JP, Lacour JR, Moyen B. Influence of maxillary mouthguards on physiological parameters. Med Sci Sports Exerc 2006; 38: 1500-1504
  • 7 Buscà B, Moreno-Doutres D, Peňa J, Morales J, Solana-Tramunt M, Aguilera-Castells J. Effects of jaw clenching wearing customized mouthguards on agility, power and vertical jump in male high-standard basketball players. JESF 2018; 16: 5-17
  • 8 Chapman PJ. Orofacial injuries and international rugby player’s attitudes to mouthguards. Br J sports Med 1990; 24: 156-158
  • 9 Collares K, Correa MB. Mohnsam da Silva IC, Hallal PC, Demarco FF. Effect of wearing mouthguards on the physical performance of soccer and futsal players: A randomized cross-over study. Dent Traumatol 2014; 30: 55-59
  • 10 Duarte-Pereira DM, Del Rey-Santamaria M, Javierre-Garcés C, Barbany-Cairó J, Paredes-Garcia J, Valmaseda-Castellón E, Berini-Aytés L, Gay-Escoda C. Wearability and physiological effects of custom-fitted vs. self-adapted mouthguards. Dent Traumatol 2008; 24: 439-442
  • 11 Dunn-Lewis C, Luk HY, Comstock BA, Szivak TK, Hooper DR, Kupchak BR, Watts AM, Putney JR, Volek JS, Denegar CR, Kraemer WJ. The effects of a customized over-the-counter mouth guard on neuromuscular force and power production in trained men and women. J Strength Cond Res 2012; 26: 1085-1093
  • 12 Ebben WP, Kaufmann CE, Fauth ML, Petushek EJ. Kinetic analysis of concurrent activation potentiation during back squats and jump squats. J Strength Cond Res 2010; 24: 1515-1519
  • 13 Evans BW, Potteiger JA. Metabolic and ventilatory responses to submaximal and maximal exercise using different breathing assemblies. J Sports Med Phys Fitness 1995; 35: 93-98
  • 14 Fédération Dentaire Internationale (FDI). Commission on dental products. working party No 7: 1990
  • 15 Francis KT, Brasher J. Physiological effects of wearing mouthguards. Br J Sports Med 1991; 25: 227-231
  • 16 Garner DP, McDivitt E. Effects of mouthpiece use on airway openings and lactate levels in healthy college males. Compend Contin Educ Dent 2009; 30: 9-13
  • 17 Garner DP, Dudgeon WD, Scheett TP, McDivitt EJ. The effects of mouthpiece use on gas exchange parameters during steady-state exercise in college-aged men and women. J Am Dent Assoc 2011; 142: 1041-1047
  • 18 Garner DP. Effects of various mouthpieces on respiratory physiology during steady-state exercise in college-aged subjects. Gen Dent 2015; 63: 30-34
  • 19 Gebauer DP, Williamson RA, Wallman KE, Dawson BT. The effect of mouthguard design on respiratory function in athletes. Clin J Sport Med 2011; 21: 95-100
  • 20 Golem DL, Arent SM. Effects of over-the-counter jaw-repositioning mouth guards on dynamic balance, flexibility, agility, strength, and power in college-aged male athletes. J Strength Cond Res 2015; 29: 500-512
  • 21 Golem DL, Davitt PM, Arent SM. The effects of over-the-counter jaw-repositioning mouthguards on aerobic performance. J Sports Phys Fitness 2017; 57: 865-871
  • 22 Harriss DJ, Macsween A, Atkinson G. Standards for ethics in sport and exercise science research: 2018 update. Int J Sports Med 2017; 38: 1126-1131
  • 23 Ilia E, Metcalfe K, Heffernan M. Prevalence of dental trauma and use of mouthguards in rugby union players. Aust Dent J 2014; 59: 473-481
  • 24 Kay EJ, Kakarla P, Macleod DA, McGlashan TP. Oro-facial and dental injuries in club rugby players. Br J Sports Med 1990; 24: 271-273
  • 25 Keçeci AD, Cetin C, Eroglu E, Baydar ML. Do custom-made mouth guards have negative effects on aerobic performance capacity of athletes?. Dent Traumatol 2005; 21: 276-280
  • 26 Knapik JJ, Marshall SW, Lee RB, Darakjy SS, Jones SB, Mitchener TA, delaCruz GG, Jones BH. Mouthguards in sport activities: History, physical properties and injury prevention effectiveness. Sports Med 2007; 37: 117-144
  • 27 Mihalik JP, McCaffrey MA, Rivera EM, Pardini JE, Guskiewicz KM, Collins MW, Lovell MR. Effectiveness of mouthguards in reducing neurocognitive deficits following sports-related cerebral concussions. Dent Traumatol 2007; 23: 14-20
  • 28 Muller-Bolla M, Lupi-Pegurier L, Pedeutour P, Bolla M. Orofacial trauma and rugby in France: epidemiological survey. Dent Traumatol 2003; 19: 183-192
  • 29 Newsome PR, Tran DC, Cooke MS. The role of the mouthguard in the prevention of sports-related dental injuries: a review. Int J Paediatr Dent 2001; 11: 396-404
  • 30 Piero M, Simone U, Jonathan M, Maria S, Giulio G, Francesco T, Gabriella C, Laura A, Eva B, Gianni N, Francesco C, Giovanni G. Influence of a custom-made maxillary mouthguard on gas exchange parameters during incremental exercise in amateur road cyclists. J Strength Cond Res 2015; 29: 672-677
  • 31 Schildknecht S, Krastl G, Kühl S, Filippi A. Dental injury and its prevention in Swiss rugby. Dent Traumatol 2012; 28: 465-469
  • 32 Schulze A, Kwast S, Busse M. Vented mouthguard effects on cardiopulmonary parameters in basketball: A pilot study. EC Dent Sci 2017; 15: 182-190
  • 33 Schulze A, Laessing J, Kwast S, Busse M. Influence of a vented mouthguard on physiological responses in handball. J Strength Cond Res 2018; 23: [Epub ahead of print]
  • 34 Tegtbur U, Busse MW, Braumann KM. Estimation of an individual equilibrium between lactate production and catabolism during exercise. Med Sci Sports Exerc 1993; 25: 620-627
  • 35 Von Arx T, Flury R, Tschan J, Buergin W, Geiser T. Exercise capacity in athletes with mouthguards. Int J sports Med 2008; 29: 435-438

Zoom Image
Fig. 1 Vented mouthguard used in this study (MGV).
Zoom Image
Fig. 2 Custom-made mouthguard used in this study (MGC).