Jian Xu, Jiming Chen, Yilu Li, Dandan Zhang, Xiaoli Li
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Pooled odds ratios and 95% confidence intervals were calculated using a fixed- or random-effects model.</p><p><strong>Results: </strong>Ten studies were identified to analyse the association between <i>ACE</i> I/D polymorphism and OSA risk. No marked associations were found in any genetic model (<i>p</i>>0.05). Subgroup analysis showed an association with hypertension (D vs. I, DD vs. II, ID vs. DD+II, DD+ID vs. II, ID vs. II; <i>p</i><0.05), which was confirmed by sensitivity analyses. No obvious publication bias was found using Egger's test (<i>p</i>>0.05).</p><p><strong>Conclusions: </strong>The <i>ACE</i> I/D polymorphism was not associated with an increased risk of OSA in a Chinese population. However, within the hypertensive subgroup, we detected a significant association between the <i>ACE</i> polymorphism and OSA. More case-control investigations are required.</p>","PeriodicalId":17330,"journal":{"name":"Journal of the Renin-Angiotensin-Aldosterone System","volume":"21 2","pages":"1470320320934716"},"PeriodicalIF":2.1000,"publicationDate":"2020-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1470320320934716","citationCount":"1","resultStr":"{\"title\":\"Association of angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea in a Chinese population: A meta-analysis.\",\"authors\":\"Jian Xu, Jiming Chen, Yilu Li, Dandan Zhang, Xiaoli Li\",\"doi\":\"10.1177/1470320320934716\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Many studies have investigated the association between angiotensin-converting enzyme (<i>ACE</i>) gene insertion/deletion (I/D) polymorphism and susceptibility to obstructive sleep apnoea (OSA). 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引用次数: 1
摘要
许多研究探讨了血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性与阻塞性睡眠呼吸暂停(OSA)易感性之间的关系。然而,很少有人证实ACE与OSA在中国人群中的关系。我们对中国人群中ACE I/D多态性与OSA风险相关的研究进行了荟萃分析。方法:我们从几个数据库中评估了符合条件的已发表研究。对高血压进行亚组分析。合并优势比和95%置信区间使用固定或随机效应模型计算。结果:10项研究分析了ACE I/D多态性与OSA风险的关系。各遗传模型均无显著相关性(p>0.05)。亚组分析显示与高血压相关(D vs. I, DD vs. II, ID vs. DD+II, DD+ID vs. II, ID vs. II;页> 0.05)。结论:在中国人群中,ACE I/D多态性与OSA风险增加无关。然而,在高血压亚组中,我们发现ACE多态性与OSA之间存在显著关联。需要进行更多的病例对照调查。
Association of angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea in a Chinese population: A meta-analysis.
Introduction: Many studies have investigated the association between angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism and susceptibility to obstructive sleep apnoea (OSA). However, few have confirmed the relationship between ACE and OSA in the Chinese population. We performed a meta-analysis of studies relating the ACE I/D polymorphism to the risk of OSA in a Chinese population.
Methods: We evaluated eligible published studies from several databases for this meta-analysis. Subgroup analyses were performed for hypertension. Pooled odds ratios and 95% confidence intervals were calculated using a fixed- or random-effects model.
Results: Ten studies were identified to analyse the association between ACE I/D polymorphism and OSA risk. No marked associations were found in any genetic model (p>0.05). Subgroup analysis showed an association with hypertension (D vs. I, DD vs. II, ID vs. DD+II, DD+ID vs. II, ID vs. II; p<0.05), which was confirmed by sensitivity analyses. No obvious publication bias was found using Egger's test (p>0.05).
Conclusions: The ACE I/D polymorphism was not associated with an increased risk of OSA in a Chinese population. However, within the hypertensive subgroup, we detected a significant association between the ACE polymorphism and OSA. More case-control investigations are required.
期刊介绍:
JRAAS is a peer-reviewed, open access journal, serving as a resource for biomedical professionals, primarily with an active interest in the renin-angiotensin-aldosterone system in humans and other mammals. It publishes original research and reviews on the normal and abnormal function of this system and its pharmacology and therapeutics, mostly in a cardiovascular context but including research in all areas where this system is present, including the brain, lungs and gastro-intestinal tract.