Association of Hypertriglyceridemic Waist Phenotype with Obstructive Sleep Apnea: A Cross-Sectional Study

被引:4
|
作者
Gu, Meizhen [1 ,2 ]
Huang, Weijun [2 ,3 ]
Li, Xinyi [2 ,3 ]
Liu, Yupu [2 ,3 ]
Wang, Fan [2 ,3 ]
Fang, Chao [2 ,4 ]
Chen, Ting [2 ,5 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Otolaryngol Head & Neck Surg, Shanghai, Peoples R China
[2] Shanghai Key Lab Sleep Disordered Breathing, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6, Dept Otolaryngol Head & Neck Surg, Shanghai, Peoples R China
[4] First Hosp Putian, Dept Otolaryngol Head & Neck Surg, Putian, Fujian, Peoples R China
[5] Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6, Dept Stomatol, Shanghai, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Otolaryngology-Head & Neck Surgery; obstructive sleep apnea; waist circumference; hypertriglyceridemia; TYPE-2; DIABETES-MELLITUS; METABOLIC SYNDROME; VISCERAL ADIPOSITY; OBESITY; RISK; PATHOGENESIS; ADULTS;
D O I
10.2147/NSS.S335288
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Hypertriglyceridemic waist (HTGW) phenotype is an independent risk factor for metabolic disorders. Although obstructive sleep apnea (OSA) is associated with metabolic disorders, it is unclear whether there is an association between HTGW phenotype and OSA. Methods: We enrolled consecutive participants presenting to a sleep center in Shanghai, China. Full-night polysomnography was performed, and serum triglyceride (TG) levels and waist circumference (WC) were calculated. HTGW phenotype was defined as increased WC (men > 90 cm, women > 80 cm) and elevated TG levels (> 1.7 mmol/L). Participants were classified into four groups: normal TG with normal WC (NTNW); normal TG with increased WC (NTGW); elevated TG with normal WC (HTNW); and elevated TG with enlarged WC, namely HTGW. The relationships between HTGW phenotypes and OSA were assessed using binary (apnea hypopnea index, [AHI]>= 5/hr) and multinomial logistic regression analyses (clinical AHI severity categories). Results: We included 3190 participants in this cross-sectional study. Compared to the NTNW phenotype, participants with NTGW and HTGW phenotypes had the significantly higher risk of OSA (AHI >= 5/hr, odds ratio [OR] = 2.51, 95% confidence interval [CI] = 1.91- 3.31; OR = 3.76, 95% CI = 2.67-5.31, respectively), after adjustment for confounders. In subgroup analyses categorised by age, sex, and BMI, the aforementioned associations remained significant. The association between the NTGW, HTGW phenotype and OSA risk remained significant across the OSA severity groups. Multinomial logistic regression also revealed that the mild (OR = 1.63, 95% CI = 1.07-2.50), moderate (OR = 1.875, 95% CI = 1.22-2.88), and severe OSA (OR = 3.18, 95% CI = 2.14-4.73) were associated with Conclusion: Both NTGW and HTGW phenotype were positively associated with OSA risk in all subgroups. Further longitudinal follow-up studies are needed to determine the causal link and prognostic role of these metabolic factors.
引用
收藏
页码:2165 / 2173
页数:9
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