The presence of tandem endothelial nitric oxide synthase gene polymorphisms identifying brain aneurysms more prone to rupture

医学 可变数串联重复 单核苷酸多态性 串联重复 基因型 优势比 SNP公司 伊诺斯 等位基因 动脉瘤 外显子 内科学 遗传学 生物信息学 病理 胃肠病学 基因 一氧化氮合酶 生物 外科 一氧化氮 基因组
作者
Vini G. Khurana,Irene Meissner,Youvraj R. Sohni,William R. Bamlet,Robyn L. McClelland,Julie M. Cunningham,Fredric B. Meyer
出处
期刊:Journal of Neurosurgery [American Association of Neurological Surgeons]
卷期号:102 (3): 526-531 被引量:52
标识
DOI:10.3171/jns.2005.102.3.0526
摘要

It is becoming apparent that the presence of certain genetic variations (polymorphisms) may increase the individual's susceptibility to cardiovascular diseases, even in the absence of a family history. We hypothesized that brain aneurysms more prone to rupture may be identified on the basis of an individual's genotype for endothelial nitric oxide synthase (eNOS), a critical vasomodulatory protein found to be increasingly relevant to the pathobiology of aneurysms.Patients' clinical data were recorded prospectively. Genomic DNA was isolated from blood samples obtained from individuals presenting consecutively to the Mayo Clinic with ruptured (58 patients) or unruptured (49 patients) intracranial saccular aneurysms. Using polymerase chain reaction and gene microarray technology, the following eNOS genetic polymorphisms were studied: intron-4 27-base pair variable number of tandem repeats (27 VNTR); promoter single nucleotide polymorphism (T-786C SNP); and exon-7 SNP (G894T SNP). Both groups of patients had similar demographic and clinical characteristics. For all three polymorphisms, variant alleles (p < or = 0.003) and their corresponding genotypes (p < or = 0.006) were found two to four times more frequently in patients with ruptured aneurysms than in patients with unruptured aneurysms. Strikingly, the odds ratio for presenting with a ruptured brain aneurysm among individuals demonstrating the copresence of all three variant alleles was 11.4 (95% confidence interval 1.7-75.9, p = 0.004).The authors have uniquely identified a set of tandem eNOS gene variations whose presence can be used to identify patients with aneurysms likely to rupture. We believe that if this finding is reproducible in a large multicenter study, in addition to known anatomical factors a rapid and cost-effective screening tool will become available to clinicians as a genetic aid to predict the risks of rupture in patients presenting with unruptured intracranial aneurysms.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
梅梅超勇敢完成签到,获得积分10
2秒前
温暖芸发布了新的文献求助10
2秒前
迷路的麋鹿完成签到 ,获得积分10
2秒前
科研通AI6.4应助滕达采纳,获得10
3秒前
3秒前
3秒前
舒心雨发布了新的文献求助10
4秒前
dddddd发布了新的文献求助10
4秒前
5秒前
假相我哥发布了新的文献求助10
6秒前
6秒前
无极微光应助香瓜采纳,获得20
7秒前
cqtwxl发布了新的文献求助10
7秒前
双马尾小男生2完成签到,获得积分10
8秒前
9秒前
可爱的函函应助pp7采纳,获得10
9秒前
云7发布了新的文献求助10
9秒前
身柏发布了新的文献求助10
10秒前
木口发布了新的文献求助10
11秒前
飞快的尔珍完成签到,获得积分20
11秒前
xiu发布了新的文献求助10
11秒前
布蓝图完成签到 ,获得积分10
11秒前
Vivilla完成签到,获得积分10
12秒前
12秒前
dddddd完成签到,获得积分10
13秒前
依古比古应助无私翅膀采纳,获得30
13秒前
cqtwxl完成签到,获得积分10
13秒前
HUSH994发布了新的文献求助10
14秒前
孤独绮梅完成签到 ,获得积分10
14秒前
负责月光发布了新的文献求助10
14秒前
乐空思应助Gray采纳,获得10
14秒前
乐空思应助Gray采纳,获得10
14秒前
耍酷的镜子完成签到,获得积分10
14秒前
14秒前
海天使完成签到,获得积分10
14秒前
15秒前
yy发布了新的文献求助10
15秒前
15秒前
碧海苍梧完成签到,获得积分10
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics: A Practical Guide 600
Research Methods for Applied Linguistics 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6405867
求助须知:如何正确求助?哪些是违规求助? 8225073
关于积分的说明 17438908
捐赠科研通 5458279
什么是DOI,文献DOI怎么找? 2884204
邀请新用户注册赠送积分活动 1860565
关于科研通互助平台的介绍 1701655