Association of obstructive sleep apnea with hypertension: A systematic review and meta-analysis.

Association of obstructive sleep apnea with hypertension: A systematic review and meta-analysis.
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DOI:
10.7189/jogh.08.010405
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发表时间:
2018-06
影响因子:
7.2
通讯作者:
Wang W
Wang W
中科院分区:
医学2区
文献类型:
--
作者:
Hou H;Zhao Y;Yu W;Dong H;Xue X;Ding J;Xing W;Wang W

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阻塞性睡眠呼吸暂停(OSA)是一种睡眠障碍,其特征是在睡眠期间完全或部分上部气流停止。虽然OSA是高血压发生的危险因素已被广泛接受,但针对该主题的研究显示了不一致的结果。我们的目的是阐明阻塞性睡眠呼吸暂停与高血压之间的关系,包括原发性高血压和耐药性高血压。遵循系统性综述和荟萃分析的首选报告项目(PRISMA)。使用PubMed和Embase数据库检索截至2016年12月31日发表的相关研究。采用Meta分析的定量方法估计合并比值比(OR)和95%置信区间(CI)。26项研究(51623例受试者,28314例男性,23309例女性;平均年龄51.8岁)符合入选标准,被纳入本研究。其中6项研究显示OSA与难治性高血压显著相关(合并OR = 2.842,95% CI = 1.703-3.980,P < 0.05)。同时,将20篇关于OSA与原发性高血压相关性的原始研究进行合并,也得到了显著的结果,合并OR为1.184轻度组为1.316(95% CI = 1.197-1.433,P <0.05),中度组为1.561(95% CI = 1.287-1.835,P < 0.05)。我们的研究结果表明,阻塞性睡眠呼吸暂停与顽固性高血压的风险增加。轻、中、重度OSA均与原发性高血压相关,并呈剂量-反应关系。这种关联在白种人和男性OSA患者中相对较强。
Obstructive sleep apnea (OSA) is a sleep disorder characterized as complete or partial upper airflow cessation during sleep. Although it has been widely accepted that OSA is a risk factor for the development of hypertension, the studies focusing on this topic revealed inconsistent results. We aimed to clarify the association between OSA and hypertension, including essential and medication-resistant hypertension. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) was followed. PubMed and Embase databases were used for searching the relevant studies published up to December 31, 2016. A quantitative approach of meta-analysis was performed to estimate the pooled odds ratio (OR) and 95% confidence interval (CI). Twenty-six studies with 51 623 participants (28 314 men, 23 309 women; mean age 51.8 years) met inclusion criteria and were included in this study. Among them, six studies showed a significant association between OSA and resistant hypertension (pooled OR = 2.842, 95% CI = 1.703-3.980, P < 0.05). Meanwhile, the combination of 20 original studies on the association of OSA with essential hypertension also presented significant results with the pooled ORs of 1.184 (95% CI = 1.093-1.274, P < 0.05) for mild OSA, 1.316 (95% CI = 1.197-1.433, P < 0.05) for moderate OSA and 1.561 (95% CI = 1.287-1.835, P < 0.05) for severe OSA. Our findings indicated that OSA is related to an increased risk of resistant hypertension. Mild, moderate and severe OSA are associated essential hypertension, as well a dose-response manner relationship is manifested. The associations are relatively stronger among Caucasians and male OSA patients.
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