Abstract
Background: Obstructive sleep apnea (OSA) is characterized by repetitive complete or partial closure of the upper airway during sleep, which is a potentially life-threatening disorder. A cephalogram is a simple and effective examination to predict the risk of OSA in orthodontic clinical practice. This study aims to analyze the relationship between craniofacial characteristics and the severity of OSA using polysomnography and cephalogram data. Gender differences in these parameters are also investigated. Methods: This study included 112 patients who underwent a complete clinical examination, standard polysomnography study, and cephalometric analysis to diagnose obstructive sleep apnea. This study divided the participants into male and female groups to study the correlation between cephalometric parameters and the severity of OSA. The analysis involved 39 cephalometric parameters. The severity of obstructive sleep apnea was evaluated by the apnea-hypopnea index (AHI) and the lowest nocturnal oxygen saturation (LSaO(2)). Results: The final assessment included 112 adult participants (male/female = 67:45, mean age: 28.4 ± 7.29 years, mean male age: 28.8 ± 7.62 years, mean female age: 27.8 ± 6.79 years). Multivariate analysis revealed that the mandibular position, incisor inclination, facial height, and maxillary first molar position were strongly associated with OSA severity. Gender-specific differences in cephalometric predictors were identified, with distinct parameters correlating with the AHI and LSaO(2) in males and females. Notably, the LSaO(2) demonstrated stronger associations with craniofacial morphology in females than males. Conclusions: Cephalometric analysis can be effective in assessing the risk and severity of OSA based on the correlation between cephalometric parameters and the AHI/LSaO(2). There is a clear difference between the cephalometric parameters associated with OSA severity in male and female individuals. This gender-dependent pattern may assist the personalized diagnosis and management of OSA in clinical practice.