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基质金属蛋白酶-1、-3、-9和-12基因多态性与蛛网膜下腔出血的关系

Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhage.

作者信息

Zhang B, Dhillon S, Geary I, Howell W M, Iannotti F, Day I N, Ye S

机构信息

Human Genetics Research Division, Clinical Neurosciences Research Division, University of Southampton, School of Medicine, UK.

出版信息

Stroke. 2001 Sep;32(9):2198-202. doi: 10.1161/hs0901.095382.

Abstract

BACKGROUND AND PURPOSE

Intracranial aneurysm, which underlies the vast majority of subarachnoid hemorrhage incidences, has a multifactorial etiology, and the importance of genetic factors is increasingly recognized. Development and rupture of intracranial aneurysms involve degradation and remodeling of the vascular wall matrix in which the matrix metalloproteinases (MMPs) play an important role. The possible impact of MMP gene polymorphisms on susceptibility to intracranial aneurysms is still controversial, with conflicting data from different reported studies.

METHODS

In this study we analyzed 5 different functional promoter polymorphisms in the MMP-1, MMP-3, MMP-9, and MMP-12 genes in a sample of 92 patients with aneurysmal subarachnoid hemorrhage and 158 healthy control subjects, all from southern England.

RESULTS

No significant difference was detected between the patient and control groups in genotype distribution of any of the polymorphisms studied.

CONCLUSIONS

The data do not support the hypothesis that MMP gene variations influence the development of intracranial aneurysms in the population studied.

摘要

背景与目的

颅内动脉瘤是绝大多数蛛网膜下腔出血病例的病因,其病因是多因素的,遗传因素的重要性日益得到认可。颅内动脉瘤的发生和破裂涉及血管壁基质的降解和重塑,其中基质金属蛋白酶(MMPs)起重要作用。MMP基因多态性对颅内动脉瘤易感性的可能影响仍存在争议,不同报道研究的数据相互矛盾。

方法

在本研究中,我们分析了来自英格兰南部的92例动脉瘤性蛛网膜下腔出血患者和158名健康对照者样本中MMP - 1、MMP - 3、MMP - 9和MMP - 12基因的5种不同功能启动子多态性。

结果

在所研究的任何多态性的基因型分布中,患者组和对照组之间均未检测到显著差异。

结论

数据不支持MMP基因变异影响所研究人群中颅内动脉瘤发生的假说。

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