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Acta Otorhinolaryngologica Italica logoLink to Acta Otorhinolaryngologica Italica
. 2017 Dec;37(6):479–485. doi: 10.14639/0392-100X-1420

Orthopaedic treatment effects of functional therapy on the sagittal pharyngeal dimensions in subjects with sleep-disordered breathing and Class II malocclusion

Effetti del trattamento ortopedico-funzionale sulle dimensioni sagittali faringee in soggetti con disturbi respiratori del sonno e malocclusione di Classe II

C Pavoni 1,, E Cretella Lombardo 1, R Lione 1, P Bollero 2, F Ottaviani 1, P Cozza 1,3
PMCID: PMC5782425  PMID: 29327733

SUMMARY

The purpose of this cephalometric study was to evaluate the craniofacial changes induced by functional treatment of mandibular advancement with special regard to pharyngeal sagittal airway dimensions, tongue and hyoid bone position in subjects with sleep-disordered breathing (SDB) and dentoskeletal Class II malocclusions compared with an untreated Class II control group. 51 subjects (24 female, 27 male; mean age 9.9 ± 1.3 years) with Class II malocclusion and SDB consecutively treated with a functional appliance (Modify Monobloc, MM) were compared with a control group of 31 subjects (15 males, 16 females; mean age 10.1 ± 1.1) with untreated Class II malocclusion. For the study group, mode of breathing was defined by an otorhinolaryngologist according to complete physical examination. The parents of all participants completed a modified version of the paediatric sleep questionnaire, PSQ-SRBD Scale, by Ronald Chervin (the Italian version in 22 items form) before and after the trial. Lateral cephalograms were available at the start and end of treatment with the MM. Descriptive statistics were used for all cephalometric measurements in the two groups for active treatment changes. Significant, favourable skeletal changes in the mandible were observed in the treated group after T2. Significant short-term changes in sagittal airway dimensions, hyoid position and tongue position were induced by functional therapy of mandibular advancement in subjects with Class II malocclusion and SDB compared with untreated controls. After orthodontic treatment, a significant reduction in diurnal symptoms was observed in 45 of the 51 participants who had received an oral appliance. Orthodontic treatment is considered to be a potential therapeutic approach for SDB in children. Orthodontists are playing an increasingly important role in managing snoring and respiratory problems by oral mandibular advancement devices and rapid maxillary expansion.

KEY WORDS: Sleep-disordered breathing, Mandibular advancement device, Functional treatment

Introduction

Sleep-disordered breathing (SDB) is a general term for breathing difficulties occurring during sleep. SDB may be defined as a disorder characterised by prolonged increased upper airway resistance, partial upper airway obstruction, or complete obstruction that disrupts pulmonary ventilation, oxygenation, or sleep quality 1.

There is a large variability in the symptoms of SDB directly related to increasing upper airway resistance. It represents a "continuum" of respiratory disorders from primary snoring to obstructive sleep apnoea (OSA) 2.

Some children compensate the airway obstruction by sleeping in a knee-chest position and with their neck hyper- extended to give the best chance of maintaining their airway while asleep 3. This form of breathing may change the growth pattern of the face and lead to morphological and functional alterations in the organism 4.

Mouth breather children develop abnormalities, such as speech disorders, facial deformities, abnormal body posture and inadequate positioning of the teeth 5 6.

Several studies examined anatomic differences between SDB subjects and nasal breathers using traditional cephalometric tracing, model analysis and three-dimensional (3D) radiography 7-13.

Model analysis revealed that SDB patients had narrower maxilla and mandible compared with the control group; the tongue may compensate for the reduced inter-arch dimensions and such as assume a more upward and backward position 14.

Cozza et al. in 2004 12 observed that the children with respiratory symptoms demonstrated a skeletal Class II pattern with a reduced mandibular length, deep overbite and the hyoid bone was located superiorly. Guilleminault et al. 15 suggested that children with retroposition of the mandible, steep mandibular plane, high hard palate, long oval-shaped face, or long soft palate were highly likely to have sleep-disordered breathing.

Kim et al. 16 in 2010 showed that the mean total airway volume, extending from the anterior nasal cavity and the nasopharynx to the epiglottis, in retrognathic patients was significantly smaller than that of patients with a normal anteroposterior skeletal relationship.

The most common cause of SDB is adenotonsillar hypertrophy. Children with adenotonsillar hypertrophy are usually treated by adenotonsillectomy (ATE). Children who do not improve after adenotonsillectomy tend to have a narrower epipharyngeal air space, a more poorly developed maxilla and mandibular retrusion 17.

Oral appliances and functional orthopaedic appliances have been used in children to shift the mandible forwards, enlarge the upper airway and improve respiratory function in patients who have OSAS and craniofacial anomalies 17 18. Mandibular advancement devices, in adult patients with mild or moderate obstructive sleep apnoea, are successful in improving AHI, and comparison with inactive appliances suggests that mandibular advancement is crucial in establishing efficacy 19 20; whereas only a few studies in the literature have evaluated mandibular advancement for treatment of respiratory difficulties in growing patients 2.

The aim of the present study was to evaluate the craniofacial changes induced by functional treatment of mandibular advancement with special regard to the pharyngeal sagittal airway dimensions, tongue and hyoid bone position in subjects with sleep-disordered breathing and dentoskeletal Class II malocclusions compared with an untreated Class II control group immediately after therapy.

Materials and methods

The study project was approved by the Ethical Committee at the Tor Vergata Hospital in Rome, and informed consent was obtained from the subjects' parents.

A sample of 90 Class II subjects was selected among patients of the Department of Orthodontics at the University of Rome Tor Vergata.

51 consecutive subjects (24 female and 27 male, mean age 9.9 ± 1.3 years), who were seen for sleep-disordered breathing, were selected for the study group and were treated for a mean period of 1.8 years (SD = 1.1) (Table I); 31 Class II subjects without SDB (15 males and 16 females, mean age 10.1 ± 1.1) were selected for comparison and were observed for a mean period of 1.9 years (SD = 0.8) (Table I). The remaining 8 subjects were excluded for the presence of systemic disorders. Demographic data of the treated and control samples are reported in Table I.

Table I.

Demographics for treatment and control group.

Age at T1, y Age at T2, y T1-T2 interval, y
Mean SD Mean SD Mean SD
Treated group 9.9 1.3 11.7 1.9 1.8 1.1
Control group 10.1 1.1 12.0 0.3 1.9 0.8

At T1, all patients had a Class II malocclusion characterised by ANB of 4° or more, overjet greater than 5 mm, full Class II or end-to-end molar relationships, deep overbite, normo-hypo divergence, no adenoidectomy or tonsillectomy, absence of previous orthodontic treatment and the absence of craniofacial syndromes.

All patients were in category 2 or 3 of the cervical vertebrae maturation indices, which indicates that they have not reached the peak pubertal growth spurt 21.

For the study group, mode of breathing was defined by an otorhinolaryngologist according to complete physical examination. The parents of all participants completed a modified version of the paediatric sleep questionnaire, PSQ-SRBD Scale, by Ronald Chervin 22 (the Italian version in 22 items form) before and after the trial. The questions sought information about child's daytime symptoms (including sleepiness, irritability, tiredness, school problems, morning headache, oral breathing, and nasal stuffiness) and night-time symptoms (including habitual snoring, apnoea, restless sleep, and nightmares).

The treatment protocols consisted of a modified monoblock (MM) made by a construction bite that positioned the mandible anteriorly in an edge to edge incisor relationship. It was fabricated from acrylic resin which is physiologically harmless, insoluble in water, odour free and inactive. The central screw was activated only once a month to follow maxillary transversal growth. Appliances were checked at regular recall.

The subjects were instructed to wear their appliances fulltime. During treatment, the absence of acrylic on the occlusal surface of posterior mandibular teeth encouraged them to erupt. The MM appliance also incorporated a Tucat's pearl on a sliding wire to determine the reference point for the tip of the tongue. Tucat's pearl allows the placement of the tongue tip against the palatal aspect of the alveolar process, behind the maxillary incisors, to improve muscle function and the habitual position of the tongue 10. Treatment with the MM appliance ended with the achievement of Class I molar relationship. After this period, subjects used the appliance at night only. To be included in the study, all the subjects had to present with lateral cephalograms available at two time periods: T1, at the start of treatment/observation period and T2, at the end of therapy/observation period.

The success of therapy in correcting the Class II malocclusion in each patient at the end of the observation period was not a determining factor for patient recruitment, an approach that lowered any potential selection bias.

The control group was observed in the same period because therapy with functional appliances was postponed to pubertal growth spurt.

Cephalometric analysis

All lateral cephalograms of each patient were hand traced at a single sitting by one investigator (ECL). Landmark location and the accuracy of the anatomical outlines were verified by a second (CP). A customized digitisation regimen (Viewbox, version 4.0, dHAL Software, Kifissia, Greece) was created and used for cephalometric evaluation.

Lateral cephalograms for each patient at T1 and T2 were digitised, and a custom cephalometric analysis was used.

The cephalometric measurements used were (Fig. 1):

Fig. 1.

Fig. 1.

a) Cephalometric analysis: Airway dimension [PNS-AD1(mm); AD1-Ba (mm); PNS-AD2 (mm); AD2-H (mm)]; b) Soft palate and oropharyngeal dimensions [MPW (mm); U-PNS; Phw1-Psp (mm); Phw2-Tb (mm)]; c) Hyoid bone [AH–C3 horizontal (mm), the horizontal distance from AH to C3; AH–C3 vertical (mm), the vertical distance from AH to C3; AH–FH (mm), the distance from AH perpendicular to Frankfort horizontal; AH–RGn (mm), the horizontal distance from AH to RGn; AH–AH1 (mm), the vertical distance from AH to the mandibular plane (AH1); AH–SN (mm), the vertical position from AH perpendicular to SN line]; d) Tongue [VT (mm); H perp VT (mm); VT^FH (degrees)].

  1. Dento-skeletal measurements: SNA°, SNB°, ANB°, Co-Me (mm), SN^Go-Gn°, FMA°, OVJ°, OVB°.

  2. Airway dimension: PNS-AD1 (mm): lower airway thickness; distance between the PNS and AD1; AD1- Ba (mm): lower adenoid thickness; PNS-AD2: upper airway thickness; AD2-H: upper adenoid thickness; Upper pharynx dimension: the minimum distance between Phw1 and Psp; Lower pharynx dimension: the minimum distance between Phw2 and Tb.

  3. Hyoid bone: AH-C3 horizontal (mm): the horizontal distance from AH to C3; AH-C3 vertical (mm): the vertical distance from AH to C3; AH-FH (mm): the distance from AH to Frankfort horizontal; AH-Rgn (mm): the horizontal position of the hyoid; AH-AH1 (mm): the vertical position of the hyoid on the mandibular plane; AH-SN (mm): the vertical position of the hyoid to the SN line.

  4. Tongue: V-T (mm): the distance from the intersection of the epiglottis and the base of the tongue to the tip of the tongue; H perpendicular to V-T: representing tongue height; V-T^FH°: representing the vertical position of the tongue.

  5. Soft palate and oropharyngeal dimensions: MPW (mm): middle pharyngeal width measured from the intersection of a perpendicular line from U to the posterior pharyngeal wall; U-PNS (mm): representing the length of the soft palate.

Method error

To analyse the error of the method, 20 randomly selected lateral cephalograms were re-digitised and re-measured within a week by the same operator.

Statistical analysis

Data analysis was performed by using the Statistical Package for Social Sciences version 22.0 software (SPSS Inc., Chicago, III). The Mann-Whitney U-test was applied to comparisons between craniofacial starting forms in the treated group vs control group. Descriptive statistics were used for all the cephalometric measurements in the two groups for the T2- T1 changes (active treatment changes). Shapiro Wilks' test revealed a normal distribution for the data. The two sample t-test was applied to compare T1-T2 changes in the treated sample vs the control group (p < 0.05). The males and females in each group were matched at T1 in terms of skeletal relationships and skeletal maturation and a student's T-test was applied at T2 to evaluate differences in skeletal relationships between the two subgroups.

Results

There were no significant differences between the treated group and the control group at study start (Table II).

Table II.

Starting forms for the treated vs control group.


Treated
group
Control
group
Mann-Whitney
U test
Dentoskeletal measurements Mean SD Mean SD
Sagittal analysis
 SNA (°) 82.5 3.0 81.5 2.6 ns
 SNB (°) 75.7 2.8 74.8 2.1 ns
 ANB (°) 6.8 1.8 6.7 1.0 ns
 Co-Me (mm) 106.8 4.8 105.61 4.5 ns
Vertical analysis
 FMA (°) 23.3 4.0 21.6 1.5 ns
 SN^GoGn 34.2 4.7 33.1 2.6 ns
 CoGoMe (°) 124.8 6.3 122.1 5.0 ns
Dental analysis
 Overjet (mm) 7.0 3.9 6.1 1.8 ns
 Overbite (mm) 5.5 2.3 5.6 1.2 ns
Hyoid
 AH-C3 hor (mm) 24.3 2.7 25.3 3.3 ns
 AH-C3 vert (mm) 2.9 4.6 2.2 4.8 ns
 AH-FH (mm) 64.0 5.2 66.0 5.4 ns
 AH-RGn (mm) 33.2 4.1 34.7 5.9 ns
 AH-AH1 (mm) 10.7 5.6 12.2 3.2 ns
 AH-SN (mm) 78.2 5.4 80 5.8 ns
Soft palate and pharynx
 U-PNS (mm) 24.8 3.5 26.3 3.4 ns
 Phw1-Psp (mm) 8.7 3.9 10.1 3.4 ns
 Phw2-Tb (mm) 10.4 3.5 11.1 2.8 ns
 MPW (mm) 5.4 2.3 6.4 2.5 ns
 PNS-AD1 (mm) 16.1 4.4 18.0 5.5 ns
 PNS-AD2 (mm) 12.1 5.9 13.2 4.1 ns
 AD1-Ba (mm) 20.9 4.7 20.9 5.2 ns
 AD2-H (mm) 13.2 4.4 14.1 3.4 ns
Tongue
 VT (mm) 60.8 2.5 59.5 4.1 ns
 H perp VT (mm) 12.3 3.5 12.3 2.7 ns
 VT^FH (°) 18.4 1.2 17.4 3.6 ns

Descriptive statistics and comparisons of the T2-T1 changes between treated and untreated control groups are given in Table III.

Table III.

Descriptive statistics and comparison of the pre-treatment and end of active treatment (T1-T2) changes between the treated and control group.


Treated
group
Control
group
2 Sample
T-test
Dentoskeletal
measurements
Mean SD Mean SD
Sagittal analysis
 SNA (°) 0,0 2.3 0.5 1.5 ns
 SNB (°) 1.5 1.6 1.2 0.3 ns
 ANB (°) -1.5 2.0 0.2 1.1 *
 Co-Me (mm) 7.1 3.0 3.0 2.4 *
Vertical analysis
 FMA (°) 0.7 3.1 0.4 2.0 ns
 SN^GoGn -0.7 2.1 -0.5 1.3 ns
 CoGoMe (°) 0.1 2.7 -1.1 2.0 ns
Dental analysis
 Overjet (mm) -2.8 3.2 0.4 1.1 *
 Overbite (mm) -1.3 2.0 0.7 1.2 *
Hyoid
 AH-C3 hor (mm) 3.3 2.2 -0.2 2.4 *
 AH-C3 vert (mm) 1.3 3.3 1.2 4.1 ns
 AH-FH (mm) 8.7 3.2 2.3 4.4 *
 AH-RGn (mm) 3.2 2.1 -0.5 4.2 *
 AH-AH1 (mm) 0.6 1.2 0.2 4.3 ns
 AH-SN (mm) 10.3 3.4 3.1 4.2 *
Soft palate and pharynx
 U-PNS (mm) 2.6 1.5 1.0 1.2 *
 Phw1-Psp (mm) 5.6 1.4 1.1 1.4 *
 Phw2-Tb (mm) 3.3 1.5 -1.0 1.2 *
 MPW (mm) 2.6 1.9 0.5 1.6 *
 PNS-AD1 2.8 1.6 2.0 1.5 *
 PNS-AD2 2.5 1.5 2.3 1.8 ns
 AD1-Ba 0.1 1.3 -1.1 1.7 *
 AD2H -0.1 1.7 -1.5 1.4 *
Tongue
 VT (mm) 6.8 2.5 1.1 2.1 *
 H perp VT (mm) -4.5 2.2 0.0 1.6 *
 VT^FH (°) -1.4 1.2 0.7 1.9 *

No significant differences between male and female subgroups were found at T2 for skeletal relationship.

Initial problems with use of MM include excessive salivation and discomfort at awakening after having a repositioning device in the mouth all night. These adverse effects were found to gradually diminish within a few days after beginning of treatment, and following this period all children and their parents reported good compliance with the MM. The appliances were, therefore, well tolerated. No dysfunctions of the dentition were noted.

The hyoid was located more anteriorly in treated patients: the value of AH-C3 horizontal presented a significant increase of + 3.6 mm in the T1-T2 period. In addition, the hyoid was found in a lower position at the end of treatment as determined from the increase of distance AH-SN and AH-FH (+ 7.2 mm and + 6.4 mm respectively).

The treated group exhibited a significant increase of the length of the soft palate (U-PNS: + 1.6 mm) and an increase of superior posterior and inferior airway space (Phw1-Psp: + 4.5 mm and Phw2-Tb: + 4.3 mm).

Middle pharyngeal width and upper airway thickness were significantly increased (MPW: + 2.1 mm; PNS-AD1: + 1.2 mm) and a reduction of upper and lower adenoid thickness (AD2-H, - 1.0 mm e AD1-Ba, - 0.4 mm) was observed.

The comparisons between the two groups showed that treated patients presented a more anterior position of the tongue (V-T, + 5.7 mm) and a reduction of its height (H perp VT, - 4,5 mm). Moreover, treated subjects presented a more lower position of the tongue as determined from the value of VT^FH (-2.2°).

When compared with controls, the treated group presented a significant decrease of -1.7° in ANB°, while mandibular length was significantly increased by + 4.0 mm (Co-Me). No significant differences were found between the two groups in vertical analysis.

Both overjet and overbite exhibited a significant improvement in treated subjects (-2.8 mm and - 1.3 mm respectively) compared to the control group.

After the trial, the children's parents again completed the same questionnaire and children underwent a new physical examination. After 1 year and 8 months of orthodontic treatment, a significant reduction in diurnal symptoms was observed in 45 of the participants who had received an oral appliance.

Thus, oral jaw positioning appliance is effective and well tolerated in the short term in children with SDB and malocclusions.

Discussion

The therapeutic effects of a mandibular advancement appliance in the treatment of obstructive sleep disorders is controversial and success rate varies substantially in clinical investigations 23 24. This might be due to differences in study protocols, appliance design and subject selection.

The purpose of this clinical trial was to evaluate the therapeutic effects of mandibular advancement on pharyngeal dimension in children with sleep-disordered breathing, treated with a Modified Monoblock.

Sleep-disordered breathing, during childhood, is often associated with hypertrophic tonsils, adenoids, retrognathic mandibles and transverse maxillary deficiencies. The retroposition of the mandibular complex was associated with reduced retrobasilingual space, mouth breathing, nasopharyngeal airway obstructions and relative retrodisplacement of the tongue. In our study, orthopaedic treatment in SDB patients exerted a direct beneficial effect with anterior repositioning of the tongue (V-T, + 5.7 mm). The rationale for selecting the MM appliance in SDB children was to modify the occlusion and increase the intermaxillary space in which the tongue rests. Linked to this was the issue of correcting the underlying skeletal Class II pattern 10 11.

According to our study, Schütz 25 observed that after mandibular advancement the anterior displacement of the mandible and hyoid bone caused an anterior traction of the tongue, which increased the posterior airway space, reduced airway resistance and facilitated nocturnal breathing. In the current study, the anterior displacement of the mandible by the functional appliances influenced the position of hyoid bone, thus improving the morphology of the upper airways 26. Our results showed that the hyoid was located more anteriorly in treated patients (AH-C3 horizontal: +3.6 mm) and in a lower position (AH-SN, + 7.2 mm; AH-FH + 6.4 mm). Schutz in 2011 evaluated the hyoid position and confirmed that the hyoid moved anteriorly but maintained its vertical position.

In our study, the treated group presented a significant decrease of ANB° (-1.7°), while mandibular length was significantly increased (Co-Me: + 4.0 mm); both overjet and overbite values exhibited a significant improvement in treated subjects (OVJ: -2.8 mm; OVB: -1,3 mm). The absence of acrylic above the mandibular posterior teeth encouraged them to erupt. The lower molars tend to come out during the treatment time. The teeth intercuspidation stabilised and gradually improved the dental occlusion 27.

These results are in agreement with those reported by confirmed by Franchi 28. He had observed, in fact, that the treated group presented with a significant increase in mandibular length and a decrease of both overjet and overbite, compared with controls.

Franchi et al. 29 in 2006 suggested that a small pre-treatment mandibular angle (Co-Go-Me angle < 125.5) was correlated with the evidence of an enhanced responsiveness to functional therapy; on the basis of this observation, we analysed the Co-Go-Me angle in our results and observed that all the Class II patients in this study are ''good responders'', confirming that these subjects are adequate for treatment with mandibular advancement.

The therapeutic benefit from early mandibular advancement may permanently modify nasal breathing and respiration, thereby preventing obstruction of the upper airway 18. It is also able to enlarge the retrolingual space and at the same time promote lingual advancement 19.

Few studies have analysed the efficacy of functional appliance treatment on pharyngeal airway dimensions in growing patients with a Class II malocclusion and a retrognathic mandible. Ozbek et al. 30 compared pharyngeal airway dimensions in 26 Class II children treated with the Harvold-type activator to 15 controls. They found that pharyngeal airway dimensions significantly increased after functional orthopaedic treatment. According to Ozbek 30, we observed that the dimension of upper and lower airways increased significantly in the treatment group with an increase of the length of the soft palate and of superior posterior and inferior airway space (U-PNS, + 1.7 mm; Phw1-Psp, + 0.5 mm; Phw2-Tb, + 0.6 mm).

The middle pharyngeal width and upper and lower airway thickness showed a significant increase (MPW, + 2.1 mm; PNS-AD1, +1.2 mm; PNS-AD2, +1.2 mm) and we also found a reduction of upper and lower adenoid thickness (AD2-H, -1.0 mm; AD1-Ba, -0.4 mm). In a study published in 2011, Restrepo et al. 31 confirmed that when the measurements before and after treatment were compared, a statistically significant increase in the airway dimensions was found at the space where the adenoid tissue was located.

Orthodontic treatment based on oral appliances is considered to be a potential additional therapeutic approach for SDB in children. Orthodontists are playing an increasingly important role in managing snoring and respiratory problems by means of oral mandibular advancement devices 19 and rapid maxillary expansion 32.

Conclusions

Correction of mandibular retrusion by using mandibular advancement appliances in Class II malocclusion subjects with sleep disorder breathings increased the airway dimensions and improved nasal breathing. The hyoid bone was found to adopt a more anterior and lower position at the end of treatment. The dimension of upper and lower airways increased significantly in the treatment group subjects compared to the control group The tongue was found to adopt a more anterior and lower position at the end of treatment. In addition, treated patients presented a significant reduction in tongue height.

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