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• W2044492372 endingPage "S375" @default.
• W2044492372 startingPage "S369" @default.
• W2044492372 abstract "Sleep disorders are a group of disorders characterized by abnormalities of respiration during sleep. OSA (Obstructive Sleep Apnea) is characterized by the repetitive episodes of complete or partial collapse of the upper airway during sleep, causing a cessation or a significant reduction of airflow.The study population consisted of 30 control patients (AHI ≤ 5) events per hour, 74 patients with OSAS, including 34 Obese (BMI ≥ 27) and 40 non-obese (BMI ≤ 27). Polysomnography and measurements of 21 cephalometric variables were carried out for all patients with OSAS.Obese patient with OSAS showed significant difference in following cephalometric parameters: (1) PAS (2) MPT (3) MPH (4) PNS-P (5) SAS. In addition, obese patient had longer tongue (TGL), more anteriorly displaced hyoid bones (H-VL) and more anterior displacement of mandible (G-VL) when compared with control groups. The findings of non-obese patients when compared to controls showed all the findings of obese patients and in addition to that narrow bony oropharynx were significant. Step wise regression analysis showed the significant predictors for all patients were MPH, PNS-P, bony nasopharynx (PNSBa), MPT, and palatal length (ANS-PNS) for AHI. The significant predictors for obese OSA (obstructive sleep apnea) group were MAS while for non-obese OSA group ANS-PNS was significant predictor for AHI (apnea-hypopnea index).Craniofacial landmarks such as increase in hyoid distance, longer tongue and soft palate with increased thickness and narrowing of superior pharyngeal, oropharyngeal and hypopharyngeal airway space may be important risk factors for development of OSAS." @default.
• W2044492372 created "2016-06-24" @default.
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• W2044492372 date "2015-12-01" @default.
• W2044492372 modified "2023-10-18" @default.
• W2044492372 title "Pharyngeal airway analysis in obese and non-obese patients with obstructive sleep apnea syndrome" @default.
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• W2044492372 doi "https://doi.org/10.1016/j.mjafi.2014.07.001" @default.
• W2044492372 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4705178" @default.
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