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血管紧张素转换酶基因插入/缺失多态性与中国人阻塞性睡眠呼吸暂停的关系:一项荟萃分析。

Association of angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea in a Chinese population: A meta-analysis.

机构信息

Department of Respiratory and Critical Care Medicine, ShenZhen Hospital of Southern Medical University, PR China.

Department of Respiratory and Critical Care Medicine, Huazhong University of Science and Technology Union Shenzhen Hospital, PR China.

出版信息

J Renin Angiotensin Aldosterone Syst. 2020 Jun 17;21(2):1470320320934716. doi: 10.1177/1470320320934716. eCollection 2020 Apr-Jun.

Abstract

INTRODUCTION

Many studies have investigated the association between angiotensin-converting enzyme () 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 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 I/D polymorphism and OSA risk. No marked associations were found in any genetic model (>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; <0.05), which was confirmed by sensitivity analyses. No obvious publication bias was found using Egger's test (>0.05).

CONCLUSIONS

The 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 polymorphism and OSA. More case-control investigations are required.

摘要

简介

许多研究调查了血管紧张素转换酶()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,很少有研究在中国人群中证实 ACE 与 OSA 之间的关系。我们对与中国人群中 I/D 多态性与 OSA 风险相关的研究进行了荟萃分析。

方法

我们从多个数据库中评估了符合条件的已发表研究,以进行荟萃分析。进行了高血压的亚组分析。使用固定或随机效应模型计算合并优势比和 95%置信区间。

结果

确定了 10 项研究来分析 I/D 多态性与 OSA 风险之间的关联。在任何遗传模型中都没有发现明显的相关性(>0.05)。亚组分析显示与高血压相关(D 与 I,DD 与 II,ID 与 DD+II,DD+ID 与 II,ID 与 II;<0.05),敏感性分析证实了这一点。Egger 检验未发现明显的发表偏倚(>0.05)。

结论

I/D 多态性与中国人群 OSA 风险增加无关。然而,在高血压亚组中,我们检测到 多态性与 OSA 之间存在显著关联。需要进行更多的病例对照研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b475/7301659/0a1d1767e113/10.1177_1470320320934716-fig1.jpg

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