Xiao Ling, Su Shuping, Liang Jia, Jiang Ying, Shu Yan, Ding Ling
Department of Otolaryngology, Children's Hospital of Chongqing Medical University, Chongqing, China.
National Clinical Research Center for Child Health and Disorders, Chongqing, China.
Front Pediatr. 2022 Jun 27;10:900216. doi: 10.3389/fped.2022.900216. eCollection 2022.
The present study was developed to explore risk factors related to the incidence and severity of obstructive sleep apnea syndrome (OSAS) in children.
The present study enrolled pediatric patients who admitted to our department for snoring and/or open-mouth breathing. All children completed a questionnaire and underwent physical examination and polysomnography (PSG). The cases were separated into OSAS and primary snoring (PS) groups. Factors associated with these two groups were analyzed, with risk factors significantly associated with OSAS then being identified through logistic regression analyses. OSAS was further subdivided into mild, moderate, and severe subgroups, with correlations between risk factors and OSAS severity then being analyzed.
In total, 1,550 children were included in the present study, of which 852 and 698 were enrolled in the OSAS and PS groups. In univariate analyses, obesity, family passive smoking, a family history of snoring, allergic rhinitis, asthma, adenoid hypertrophy, and tonsil hypertrophy were all related to pediatric OSAS ( < 0.05). In a multivariate logistic regression analysis, adenoid hypertrophy (OR:1.835, 95% CI: 1.482-2.271) and tonsil hypertrophy (OR:1.283, 95% CI:1.014-1.622) were independently associated with the risk of pediatric OSAS ( < 0.05). Stratification analyses revealed that OSAS incidence increased in a stepwise manner with increases in adenoid and tonsil grading ( < 0.01). Correlation analyses revealed that adenoid hypertrophy and tonsilar hypertrophy were not significantly associated with OSAS severity ( = 0.253, 0.069, respectively, < 0.05), and tonsil and adenoid size were no correlation with obstructive apnea-hypopnea index (OAHI) ( = 0.237,0.193, respectively, < 0.001).
Obesity, family passive smoking, a family history of snoring, allergic rhinitis, asthma, tonsil hypertrophy, and adenoid hypertrophy may be potential risk factors for pediatric OSAS. Adenoid hypertrophy and tonsil hypertrophy were independently related to the risk of pediatric OSAS, with OSAS incidence increasing with the size of the adenoid and tonsil, while the severity of OSAS is not parallel related to the adenoid or tonsil size.
开展本研究以探索与儿童阻塞性睡眠呼吸暂停综合征(OSAS)发病率及严重程度相关的危险因素。
本研究纳入因打鼾和/或张口呼吸而入住我科的儿科患者。所有儿童均完成一份问卷,并接受体格检查及多导睡眠图(PSG)检查。将病例分为OSAS组和原发性打鼾(PS)组。分析与这两组相关的因素,然后通过逻辑回归分析确定与OSAS显著相关的危险因素。OSAS进一步细分为轻度、中度和重度亚组,随后分析危险因素与OSAS严重程度之间的相关性。
本研究共纳入1550名儿童,其中852名和698名分别纳入OSAS组和PS组。在单因素分析中,肥胖、家庭被动吸烟、打鼾家族史、过敏性鼻炎、哮喘、腺样体肥大和扁桃体肥大均与儿童OSAS相关(P<0.05)。在多因素逻辑回归分析中,腺样体肥大(OR:1.835,95%CI:1.482 - 2.271)和扁桃体肥大(OR:1.283,95%CI:1.014 - 1.622)与儿童OSAS风险独立相关(P<0.05)。分层分析显示,OSAS发病率随腺样体和扁桃体分级增加而呈逐步上升趋势(P<0.01)。相关性分析显示,腺样体肥大和扁桃体肥大与OSAS严重程度无显著相关性(分别为P = 0.253、0.069,P<0.05),且扁桃体和腺样体大小与阻塞性呼吸暂停低通气指数(OAHI)无相关性(分别为P = 0.237、0.193,P<0.001)。
肥胖、家庭被动吸烟、打鼾家族史、过敏性鼻炎、哮喘、扁桃体肥大和腺样体肥大可能是儿童OSAS的潜在危险因素。腺样体肥大和扁桃体肥大与儿童OSAS风险独立相关,OSAS发病率随腺样体和扁桃体大小增加而上升,而OSAS严重程度与腺样体或扁桃体大小无平行关系。