|Year : 2015 | Volume
| Issue : 4 | Page : 331-336
Comparative evaluation of craniofacial anthropometric measurements in Indian adult patients with and without obstructive sleep apnea: A pilot study
Abhishek Dubey1, Snehal Upadhyay2, Somil Mathur2, Surya Kant1, Balendra Pratap Singh3, Rakesh Makwana2
1 Department of Pulmonary Medicine, King George's Medical University, Lucknow, Uttar Pradesh, India
2 Department of Prosthodontics and Oral Implantology, Faculty of Dental Sciences, Dharamsinh Desai University, Nadiad, Gujarat, India
3 Department of Prosthodontics, King George's Medical University, Lucknow, Uttar Pradesh, India
|Date of Submission||05-Apr-2015|
|Date of Acceptance||11-Jun-2015|
|Date of Web Publication||14-Dec-2015|
B-10, Nipa Tenements-1, Opp. Sahyog Society, Gorwa-Refinery Road, Vadodara, Gujarat
Source of Support: None, Conflict of Interest: None
Aims: The study aimed to compare the craniofacial features of North Indian patients suffering from obstructive sleep apnea (OSA) to that of normal North Indian population.
Materials and Methods: Selected 25 North Indian subjects (age: 18–65 years) were divided into two groups (OSA group [n = 14] and non-OSA group [n = 9]) according to the results of full night polysomnographic sleep study. Body mass index (BMI), neck circumference (NC), and lateral cephalograms were recorded for each subject in both groups and total 22 parameters of craniofacial anthropometric features were measured on lateral cephalograms for each subject. The differences in BMI, NC, and craniofacial features between the OSA and non-OSA groups were compared statistically.
Results: Independent sample t-test was used to compare the differences between OSA group and non-OSA group. The results showed that the BMI, NC, bulk of tongue (tongue length, tongue height, and tongue area) and length of the soft palate (PNS-U) were significantly higher in OSA group. OSA group was also found to have inferior positioning of hyoid bone (MP-H, ANS-H, PNS-H, ANS-Eb), narrower superior and middle airway space (SPAS and MAS), antero-inferior positioning of mandible (Gn-C3, ANS-Me, SNB, N-Me) and lower cranial base flexure angle (N-S-Ba).
Conclusion: Craniofacial features, which play an important role in the pathophysiology of OSA, differ significantly between North Indian patients suffering from OSA and normal North Indian population.
Keywords: Body mass index, craniofacial features, lateral cephalogram, neck circumference, obstructive sleep apnea
|How to cite this article:|
Dubey A, Upadhyay S, Mathur S, Kant S, Singh BP, Makwana R. Comparative evaluation of craniofacial anthropometric measurements in Indian adult patients with and without obstructive sleep apnea: A pilot study. J Indian Prosthodont Soc 2015;15:331-6
|How to cite this URL:|
Dubey A, Upadhyay S, Mathur S, Kant S, Singh BP, Makwana R. Comparative evaluation of craniofacial anthropometric measurements in Indian adult patients with and without obstructive sleep apnea: A pilot study. J Indian Prosthodont Soc [serial online] 2015 [cited 2019 Sep 20];15:331-6. Available from: http://www.j-ips.org/text.asp?2015/15/4/331/161567
| Introduction|| |
Sleep-disordered breathing is a series of disorders ranging from primary snoring to severe obstructive sleep apnea-hypopnea syndrome (OSAHS). The OSAHS is characterized by recurring episodes of upper airway obstruction during sleep, leading to markedly reduced (hypopnea) or absent (apnea) airflow at the nose/mouth leading to sleep fragmentation. It is thought to be due to varying combinations of anatomical and neuromuscular factors resulting in complete or partial obstruction of the airway.
Obstructive sleep apnea is a common disorder with variable prevalence rates among different ethnic populations. A community-based study of Chinese population showed an overall prevalence rate of 20.4%. A community-based study of sleep apnea among middle-aged Chinese men in Hong Kong using full polysomnography demonstrated an estimated prevalence of OSA at 4.1%. Similar study in middle-aged Chinese women in Hong Kong demonstrated an estimated prevalence of OSA at 2.1%. A community-based study of OSA with fully supervised PSG showed overall prevalence rate of 13.74% (19.7% in men, 7.4% in women) in North-Indian population. However, a similar study in the same population showed overall prevalence rate of OSA 9.3% (13.5% in men, 5.6% in women). A hospital-based study of OSA with unsupervised PSG found the prevalence rate of 19.5% in middle-aged urban Indian men. Snoring is even more common affecting 40–60% of adults. OSA is characterized by increased effort of respiration, reduced blood oxygen saturation and frequent disturbances in normal sleep and arousals during sleep. Snoring, excessive daytime sleepiness, early morning headaches, impaired concentration, social impairments, systemic and pulmonary hypertension, traffic and work-related accidents, ischemic heart disease, and cerebrovascular disease, are often associated with this syndrome., Severity of OSA can be assessed by Apnea/Hypopnea Index (AHI). AHI is calculated by overnight polysomnography analysis. AHI <5 events/h, is considered to be normal. OSA can be classified as mild (AHI = 5–15 events/h), moderate (AHI = 15–30 events/h), and severe (AHI = more than 30 events/h). The pathogenesis of this syndrome is still not entirely clear. During sleep, tongue base contacts the posterior pharyngeal wall and occludes the upper airway partially or completely. Further, relaxation of the genioglossus and pharyngeal muscles leading to diminution of upper airway dilator muscle activity, which counteracts the negative intra-luminal pharyngeal pressure during sleep may result in pharyngeal collapse and obstruction in patients with OSA. However, this mechanism depends on the morphology of craniofacial skeleton and oro-facial musculature.
Many other studies have also found that the interrelationship of craniofacial morphology and muscle function of the upper airway is important in the understanding pathogenesis behind OSA. Different ethnic groups have significant differences in craniofacial as well as general body skeletal and soft tissue features. These ethnic differences in craniofacial morphology greatly affect airway dimensions and consequently AHI. Brachycephaly is associated with an increased AHI in Caucasians, but not in Afro-Americans. Asian males are less obese despite the presence of severe OSA as compared to Caucasian males. Craniofacial morphology differences have also been noted among OSA-subjects of three major ethnic populations in Asia.
Since craniofacial features differ among ethnic populations, specific characteristics for each population might suggest the risk for OSA in concerned ethnic population and requires further diagnostic interventions for definitive diagnosis of OSA. Thus, craniofacial features being important risk factor for OSA should be investigated intra-ethnically as well. Hence, the aim of this study was to compare the difference in the craniofacial features of North Indian patients with OSA and non-OSA subjects.
| Materials and Methods|| |
Totally 25 North Indian subjects in the age group of 18–65 years were included in this cross-sectional study through simple random sampling representing general population of the above-mentioned age group as OSA is prevalent in middle-aged population.
- Subjects with psychiatric illness and taking central nervous system (CNS) depressants
- Subjects who consumed alcohol (not avoided it for at least 1 week prior to the overnight sleep study)
- Subjects who had uncontrolled systemic disease
- Subjects with craniofacial anomalies associated with syndromes, such as Crouzon syndrome, Apert Syndrome, Treacher–Collins Syndrome
- Subjects who were snorers only or who had mixed sleep apnea (which includes CNS component in the pathophysiology of sleep apnea).
Informed consent was obtained from the patients and ethical approval was obtained from Institutional Ethical Committee. Poststratification of the sample population was done using polysomnographic analysis to divide the population in OSA group and non-OSA group.
All subjects underwent full night polysomnography sleep study (S-7000, Cogent technologies, EMBLA System Inc., UK), which includes electroencephalograms, (C3-A2, C4-A1, O2-A1, O3-A2), Bilateral Electro-oculogram (ROC, LOC), Chin and Leg Electromyogram, Nasal airflow, thoracic and abdominal movements, electrocardiogram, O2 saturation measured by finger pulse oximeter and body position recorders. AHI was calculated with the help of Somnologica Studio Software (EMBLA System Inc., UK). The apnea episodes were defined as complete cessation of airflow for ≥10 s, and hypopnea was defined as a ≥50% reduction in oro-nasal airflow accompanied by a reduction of at least 4% oxygen saturation calculated by pulse oximetry. Apnea events were classified as obstructive, mixed, or central, according to the presence or absence of breathing efforts with thoraco-abdominal movements. AHI was determined by the frequency of these events per hour during sleep time based on the results of the overnight polysomnography. Recorded polysomnographic data were cross-checked manually for scoring of sleep stages, apnea and hypopnea events regarding each subject. Two subjects with mixed sleep apnea were excluded from this study.
Based on AHI calculated from polysomnography, subjects were divided in two groups: OSA group – AHI >5 (14 subjects) and non-OSA group – AHI <5 (9 subjects). The body mass index (BMI) was calculated in kg/m 2, and neck circumference (NC) was measured at the level of the thyroid cartilage.
The polysomnography was followed by taking lateral cephalograms (Gendex Digital System, Hamburg, Germany) utilizing standardization parameters. Each lateral cephalogram was taken with the Frankfort Horizontal Plane oriented parallel to the floor and teeth in maximum intercuspation. To standardize the position of the hyoid bone, the patient was requested to inhale slowly and then exhale just before exposing the film. All the cephalograms were analyzed by a single observer in the morning (between 9 am and 11 am). Due care was taken to conceal participant identity to prevent future observer bias. Landmarks and reference lines were then drawn on acetate tracing sheets for taking linear, angular and areal measurements. Cephalometric analysis was performed by plotting soft tissue and hard tissue landmarks [Table 1], [Figure 1] and [Figure 2].
Statistical analysis was performed using the Statistical Package for Social Services version 12.0 software (SPSS Inc., Chicago, Illinois, USA). Independent sample t-test was used to compare craniofacial differences between the OSA and non-OSA groups. The level of significance was set at 0.05.
| Results|| |
Body mass index and NC are the parameters of outmost importance when considered as screening parameters for diagnosis of OSA. BMI and NC were found to be significantly higher in OSA group when compared to non-OSA group (P < 0.001) [Table 2].
Higher tongue volume being a cause of obstruction for airway is significant risk factor for OSA. Thickness (tongue height) and length (tongue length) of tongue were found to be significantly higher in OSA group (P = 0.006, <0.001, respectively). Furthermore, total tongue area (TA) was also found to be higher in OSA group (P = 0.001) [Table 3].
OSA group also have significantly less antero-posterior dimension of superior airway space (SPAS), and middle airway space (MAS) when compared to non-OSA group (P < 0.001), but the difference between inferior airway spaces (IAS-1 and IAS-2) was found to be insignificant [Table 3].
Position of the hyoid bone was also found to be significantly lower in OSA group (MP-H, ANS-H, PNS-H, ANS-Eb) (P < 0.001). OSA group patient also showed infero-posterior position of mandible when compared to non-OSA group (Gn-C3, ANS-Me [P < 0.001] and SNB, N-Me [P = 0.043 andP = 0.005, respectively]) [Table 4].
When compared to OSA group, length of soft palate (PNS-U) was found to be shorter in non-OSA group (P < 0.001). The cranial base flexure angle (N-S-Ba) was significantly lower in OSA group when compared to non-OSA group (P < 0.001). Patients in OSA group had significant posterior positioning of maxilla and mandible with reference to cranium (P = 0.031 andP = 0.043, respectively). In contrast, antero-posterior position of mandible with reference to maxilla did not differ significantly (P = 0.0332) [Table 4].
| Discussion|| |
Due to increase in number of patients suffering from OSA and lack of awareness about the disease, the screening of such patients in day to day medical as well as dental practice is very essential to tackle this life-threatening disease. There are certain craniofacial features, which are different in individuals suffering from OSA when compared to normal population. Identifying such patients through the knowledge of these features can help a practitioner identify them and treat them in an appropriate way. However, these craniofacial features vary from one ethnicity to another. So, these features should be studied by comparing individuals suffering from OSA to the normal individuals. Indian population differs significantly from other ethnic populations in craniofacial features.
Body mass index and NC are the basic parameter of obesity, which is most commonly related to OSA., Obesity is a common factor associated with OSA and it is more prevalent in Caucasian population. Although higher BMI is related to apnea severity in Asian population also, correlation between BMI and apnea severity is weaker in the Asian population. The results of this study demonstrate that BMI and NC were significantly higher in this Indian OSA group than in the non-OSA group. In the supine position, the tongue fall back posteriorly and obstruct the hypopharyngeal space., Furthermore, relaxation of tongue musculature during sleep significantly increases this back-fall of tongue. Severity of obstruction of airway depends on bulk of tongue and amount of relaxation of tongue musculature. Bulk of tongue being a cause of obstruction for airway has a significant effect on apnea severity. The study showed significantly longer length and thickness of tongue in OSA group patients resulting in narrow airway space. These features of tongue are closely related to increase in BMI and NC.
The OSA patients in this study showed significantly longer soft palate, which occupied more space in the oropharyngeal area. Studies had indicated that continuous vibration of the soft palate during snoring leads to continuous trauma and causes mucosal edema, further reducing upper airway patency. The increased muscular stiffness of the soft palate suggests that its tissues undergo morphological and functional changes, supported by the histological findings of the uvular and soft palate muscles in snoring and apneic patients obtained at biopsy following uvulopalatopharyngoplasty. Antero-posterior as well as lateral dimensions of airway are one of the most important predictors of apnea severity. It also helps to identify the subjects with increased OSA risk as well as to select the most appropriate modality of treatment, especially for surgical procedures. Within limitations of the study, OSA group also have a significantly less antero-posterior dimension of SPAS and MAS when compared to non-OSA group. Lateral dimensions of the airway space can be further evaluated in three-dimensional (3D) imaging techniques like computed tomography (CT), cone bean computed tomography (CBCT), magnetic resonance imaging (MRI), etc.
The hyoid bone in OSA patients was more inferiorly and posteriorly positioned as compared to non-OSA group thus encroaching onto airway space significantly. As the hyoid bone serves for anchorage of tongue muscles, infero-posterior displacement of hyoid pulls the muscles of the tongue into a downward and backward position resulting in a greater tongue mass in OSA patients.,, Wong et al. found that the hyoid bone was located more posteriorly in Chinese OSA subjects when compared with Malays and Indians.
An acute cranial base angle decreases the antero-posterior length of pharynx and will cause anterior displacement of posterior pharyngeal wall leading to obstruction of airway. This study also showed a more acute cranial base flexure angle (N-S-Ba) as well as narrower upper and MASs in OSA subjects than the non-OSA group. Because the upper airway is a soft tube without bony support, any changes in the cross-sectional area and radius of curvature can affect the dimensions of the upper airway. The result of the present study showed that the angle between the anterior and posterior segments of the cranial base was diminished resulting in the cervical spine at C3 level and posterior pharyngeal wall being further forward, thus reducing the space available for the airway.
Significant posterior positioning of mandible, as well as maxilla, was observed in OSA group suggesting posterior positioning of tongue hyoid complex. Maeda et al. found the same while comparing obese and nonobese Japanese OSA patients. They also noted a decreased bony pharynx width, which might reflect a posterior positioning of the maxilla and mandible. Lower facial height may also increase with increased facial convexity suggesting inferior and posterior placement of hyoid bone and base of tongue in OSA patients. This leads to narrowed bony inlet of the pharyngeal airway representing an inherent risk factor for the development of airway obstruction. Sforza et al. found no significant differences in lower and total facial heights between obese and nonobese OSA patients of the same height. This may provide a mean to reposition the maxilla and mandible with help of orthodontics and orthopedics and resolve the problem of airway narrowing to a great degree.
The study has limited sample size and has utilized lateral cephalogram as tool for evaluation of craniofacial dimensions. Lateral cephalometry provides only two-dimensional views. Further studies with large sample size using CT, CBCT, and MRI are required for 3D information of the craniofacial features.
Moreover, until date there are no established guidelines for appliance selection for an individual OSA patient. Further studies comparing efficacy of different oral appliances for management of OSA for patients with different craniofacial features may enlighten the criteria for appliance selection for patient with particular craniofacial feature and help dental sleep medicine specialist to establish an individualized approach in management of OSA.
| Conclusion|| |
Within limitations of the study, Indian OSA subjects had significant hard and soft tissue differences when compared with non-OSA subjects. Thus, craniofacial abnormalities play a significant role in the pathogenesis of OSA. A thorough knowledge of these features can play an important role in understanding the complex pathophysiology of OSA and can help in appliance selection for a particular patient.
- North Indian OSA patients have higher BMI, NC and TA than normal individuals have
- North Indian OSA patients have inferiorly positioned hyoid bone, longer soft palate and acute cranial base flexure angle when compared to normal individuals
- North Indian OSA patients have constricted upper and MAS
- North Indian OSA patients have posteriorly positioned maxilla and mandible than normal North Indian population.
| References|| |
Berry RB, Budhiraja R, Gottlieb DJ, Gozal D, Iber C, Kapur VK, et al.
Rules for scoring respiratory events in sleep: Update of the 2007 AASM Manual for the Scoring of Sleep and Associated Events. Deliberations of the Sleep Apnea Definitions Task Force of the American Academy of Sleep Medicine. J Clin Sleep Med 2012;8:597-619.
Huang SG, Li QY, Sleep Respiratory Disorder Study Group Respiratory Disease Branch Shanghai Medical Association. Prevalence of obstructive sleep apnea-hypopnea syndrome in Chinese adults aged over 30 yr in Shanghai. Zhonghua Jie He He Hu Xi Za Zhi 2003;26:268-72.
Ip MS, Lam B, Lauder IJ, Tsang KW, Chung KF, Mok YW, et al.
A community study of sleep-disordered breathing in middle-aged Chinese men in Hong Kong. Chest 2001;119:62-9.
Ip MS, Lam B, Tang LC, Lauder IJ, Ip TY, Lam WK. A community study of sleep-disordered breathing in middle-aged Chinese women in Hong Kong: Prevalence and gender differences. Chest 2004;125:127-34.
Sharma SK, Kumpawat S, Banga A, Goel A. Prevalence and risk factors of obstructive sleep apnea syndrome in a population of Delhi, India. Chest 2006;130:149-56.
Reddy EV, Kadhiravan T, Mishra HK, Sreenivas V, Handa KK, Sinha S, et al.
Prevalence and risk factors of obstructive sleep apnea among middle-aged urban Indians: A community-based study. Sleep Med 2009;10:913-8.
Udwadia ZF, Doshi AV, Lonkar SG, Singh CI. Prevalence of sleep-disordered breathing and sleep apnea in middle-aged urban Indian men. Am J Respir Crit Care Med 2004;169:168-73.
Kang K, Seo JG, Seo SH, Park KS, Lee HW. Prevalence and related factors for high-risk of obstructive sleep apnea in a large korean population: Results of a questionnaire-based study. J Clin Neurol 2014;10:42-9.
Olaithe M, Bucks RS. Executive dysfunction in OSA before and after treatment: A meta-analysis. Sleep 2013;36:1297-305.
Mesarwi O, Polak J, Jun J, Polotsky VY. Sleep disorders and the development of insulin resistance and obesity. Endocrinol Metab Clin North Am 2013;42:617-34.
Hillman DR, Walsh JH, Maddison KJ, Platt PR, Schwartz AR, Eastwood PR. The effect of diaphragm contraction on upper airway collapsibility. J Appl Physiol 2013;115:337-45.
Chowdhuri S, Pierchala L, Aboubakr SE, Shkoukani M, Badr MS. Long-term facilitation of genioglossus activity is present in normal humans during NREM sleep. Respir Physiol Neurobiol 2008;160:65-75.
Finkelstein Y, Wolf L, Nachmani A, Lipowezky U, Rub M, Shemer S, et al.
Velopharyngeal anatomy in patients with obstructive sleep apnea versus normal subjects. J Oral Maxillofac Surg 2014;72:1350-72.
Lee RW, Vasudavan S, Hui DS, Prvan T, Petocz P, Darendeliler MA, et al.
Differences in craniofacial structures and obesity in Caucasian and Chinese patients with obstructive sleep apnea. Sleep 2010;33:1075-80.
Wong ML, Sandham A, Ang PK, Wong DC, Tan WC, Huggare J. Craniofacial morphology, head posture, and nasal respiratory resistance in obstructive sleep apnoea: An inter-ethnic comparison. Eur J Orthod 2005;27:91-7.
Dixon J, Schachter L, O'Brien P. Predicting sleep apnoea and excessive day sleepiness in the severely obese. Chest 2002;123:134-41.
Ferguson KA, Ono T, Lowe AA, Ryan CF, Fleetham JA. The relationship between obesity and craniofacial structure in obstructive sleep apnea. Chest 1995;108:375-81.
Dempsey JA, Veasey SC, Morgan BJ, O'Donnell CP. Pathophysiology of sleep apnea. Physiol Rev 2010;90:47-112.
Brennick MJ. Understanding airway tissue mechanics is a step towards improving treatments in OSA. Sleep 2013;36:973-74.
Veldi M, Vasar V, Vain A, Kull M. Obstructive sleep apnea and ageing Myotonometry demonstrates changes in the soft palate and tongue while awake. Pathophysiology 2004;11:159-65.
Togeiro SM, Chaves CM Jr, Palombini L, Tufik S, Hora F, Nery LE. Evaluation of the upper airway in obstructive sleep apnoea. Indian J Med Res 2010;131:230-5.
Battagel JM, Johal A, Kotecha B. A cephalometric comparison of subjects with snoring and obstructive sleep apnoea. Eur J Orthod 2000;22:353-65.
Maschtakow PS, Tanaka JL, da Rocha JC, Giannas LC, de Moraes ME, Costa CB, et al.
Cephalometric analysis for the diagnosis of sleep apnea: A comparative study between reference values and measurements obtained for Brazilian subjects. Dental Press J Orthod 2013;18:143-9.
Tsuiki S, Lowe AA, Almeida FR, Fleetham JA. Effects of an anteriorly titrated mandibular position on awake airway and obstructive sleep apnea severity. Am J Orthod Dentofacial Orthop 2004;125:548-55.
Maeda K, Tsuiki S, Isono S, Namba K, Kobayashi M, Inoue Y. Difference in dental arch size between obese and non-obese patients with obstructive sleep apnoea. J Oral Rehabil 2012;39:111-7.
Enacar A, Aksoy AU, Sençift Y, Haydar B, Aras K. Changes in hypopharyngeal airway space and in tongue and hyoid bone positions following the surgical correction of mandibular prognathism. Int J Adult Orthodon Orthognath Surg 1994;9:285-90.
Sforza E, Bacon W, Weiss T, Thibault A, Petiau C, Krieger J. Upper airway collapsibility and cephalometric variables in patients with obstructive sleep apnea. Am J Respir Crit Care Med 2000;161:347-52.
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4]