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基质金属蛋白酶-9启动子基因多态性与阻塞性睡眠呼吸暂停综合征的关联性缺失

Lack of association of matrix metalloproteinase-9 promoter gene polymorphism in obstructive sleep apnea syndrome.

作者信息

Yalcınkaya Mustafa, Erbek Selim S, Babakurban Seda Turkoglu, Kupeli Elif, Bozbas Serife, Terzi Yunus K, Sahin Feride Iffet

机构信息

Department of Otorhinolaryngology, Faculty of Medicine, Baskent University, 06490, Ankara, Turkey.

Department of Pulmonary Medicine, Faculty of Medicine, Baskent University, 06490, Ankara, Turkey.

出版信息

J Craniomaxillofac Surg. 2015 Sep;43(7):1099-103. doi: 10.1016/j.jcms.2015.06.014. Epub 2015 Jun 23.

Abstract

PURPOSE

Obstructive sleep apnea syndrome (OSAS) is a public health problem. There is an effort to establish the genetic contributions to the development of OSAS. One is matrix metalloproteinases, extracellular matrix degrading enzymes related to systemic inflammation. However, the impact of matrix metalloproteinase-9 (MMP-9) genotypes on the development of OSAS is unknown. Our aim was to determine whether MMP-9 single nucleotide polymorphism (SNP) (MMP-9 -1562C > T) is related to susceptibility to OSAS.

MATERIAL AND METHODS

A total of 106 patients with a history of sleep apnea and 88 controls without a history of sleep apnea were enrolled in this study. Genotypes were determined by restriction fragment length polymorphism analyses after polymerase chain reaction.

RESULTS

Genotypes and allele frequencies of the MMP-9 -1562C > T SNP was not statistically different between the patient and control groups (p > 0.05). There was a statistical association between apnea-hypopnea index (AHI) and body mass index (BMI), and also between AHI and neck circumference (p < 0.001). There was no association among the genotypes and AHI, neck circumference, or BMI (p > 0.05).

CONCLUSIONS

We found no association between MMP-9 -1562C > T SNP and OSAS. Studies to investigate the role of other polymorphisms and expression of MMP-9 gene will provide more information.

摘要

目的

阻塞性睡眠呼吸暂停综合征(OSAS)是一个公共卫生问题。目前正在努力确定基因对OSAS发生发展的影响。其中之一是基质金属蛋白酶,这是一种与全身炎症相关的细胞外基质降解酶。然而,基质金属蛋白酶-9(MMP-9)基因型对OSAS发生发展的影响尚不清楚。我们的目的是确定MMP-9单核苷酸多态性(SNP)(MMP-9 -1562C>T)是否与OSAS易感性相关。

材料与方法

本研究共纳入106例有睡眠呼吸暂停病史的患者和88例无睡眠呼吸暂停病史的对照者。通过聚合酶链反应后的限制性片段长度多态性分析确定基因型。

结果

患者组和对照组之间MMP-9 -1562C>T SNP的基因型和等位基因频率无统计学差异(p>0.05)。呼吸暂停低通气指数(AHI)与体重指数(BMI)之间以及AHI与颈围之间存在统计学关联(p<0.001)。基因型与AHI、颈围或BMI之间无关联(p>0.05)。

结论

我们发现MMP-9 -1562C>T SNP与OSAS之间无关联。研究其他多态性的作用以及MMP-9基因的表达将提供更多信息。

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