Department of Maternal and Child Health Care, School of Public Health, Shandong University, Jinan, China; Department of Nutrition and Food Hygiene and Ministry of Education Key Lab of Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Int J Cardiol. 2013 Nov 5;169(3):207-14. doi: 10.1016/j.ijcard.2013.08.088. Epub 2013 Sep 8.
The association between obstructive sleep apnea (OSA) and the incidence of cardiovascular disease (CVD) has been examined in many studies. However, the findings are not entirely consistent across studies. Our goal was to evaluate the association between OSA and risk of CVD and all-cause mortality by performing a meta-analysis of prospective cohort studies.
We used generalized least squares regression models to estimate the dose-response relationship. Heterogeneity, subgroup, and sensitivity analyses and publication bias were performed.
Twelve prospective cohort studies involving 25,760 participants were included in the meta-analysis. The overall combined relative risks for individuals with severe OSA compared with individuals with an AHI of <5 were 1.79 (95% confidence interval [CI]: 1.47 to 2.18) for CVD, 1.21 (95% CI: 0.75 to 1.96) for incident fatal and non-fatal coronary heart disease, 2.15 (95% CI: 1.42 to 3.24) for incident fatal and non-fatal stroke, and 1.92 (95% CI: 1.38 to 2.69) for deaths from all-causes. A positive association with CVD was observed for moderate OSA but not for mild OSA. The results of the dose-response relationship indicated that per 10-unit increase in the apnea-hypopnea index was associated with a 17% greater risk of CVD in the general population.
This meta-analysis of prospective cohort studies suggests that severe OSA significantly increases CVD risk, stroke, and all-cause mortality. A positive association with CVD was observed for moderate OSA but not for mild OSA.
阻塞性睡眠呼吸暂停(OSA)与心血管疾病(CVD)的发生之间的关系已在许多研究中进行了检查。然而,研究结果并不完全一致。我们的目标是通过对前瞻性队列研究进行荟萃分析来评估 OSA 与 CVD 和全因死亡率的相关性。
我们使用广义最小二乘法回归模型来估计剂量反应关系。进行了异质性、亚组和敏感性分析以及发表偏倚。
共纳入了 12 项涉及 25760 名参与者的前瞻性队列研究。与 AHI<5 的个体相比,严重 OSA 个体的总体合并相对风险为 CVD 1.79(95%置信区间[CI]:1.47 至 2.18),致命和非致命冠心病 1.21(95%CI:0.75 至 1.96),致命和非致命性中风 2.15(95%CI:1.42 至 3.24)以及所有原因的死亡率为 1.92(95%CI:1.38 至 2.69)。中度 OSA 与 CVD 呈正相关,但轻度 OSA 则不然。剂量反应关系的结果表明,在一般人群中,每增加 10 个单位的呼吸暂停低通气指数,与 CVD 风险增加 17%相关。
这项对前瞻性队列研究的荟萃分析表明,严重 OSA 可显著增加 CVD 风险、中风和全因死亡率。中度 OSA 与 CVD 呈正相关,但轻度 OSA 则不然。