STROKE:多基因风险评分系统评估缺血性脑卒中的基因易感性

2017-03-06 luowenbo MedSci原创

多基因风险评分系统评估缺血性脑卒中的基因易感性通过评估缺血性脑卒中(IS)的基因易感性可以筛选出缺血性脑卒中高风险人群,并提前进行临床干预。然而,使用先前开发的加权多位点基因风险评分系统预测IS风险具有一定的局限性。为了更准确预测IS风险,本研究使用一种新的IS风险评分方法-多基因风险评分系统(polyGRS),并对该方法的IS风险预测能力进行验证。多基因风险评分系统(polyGRS)通过对大量I

多基因风险评分系统评估缺血性脑卒中的基因易感性

通过评估缺血性脑卒中(IS)的基因易感性可以筛选出缺血性脑卒中高风险人群,并提前进行临床干预。然而,使用先前开发的加权多位点基因风险评分系统预测IS风险具有一定的局限性。为了更准确预测IS风险,本研究使用一种新的IS风险评分方法-多基因风险评分系统(polyGRS),并对该方法的IS风险预测能力进行验证。多基因风险评分系统(polyGRS)通过对大量IS强基因信号因子与IS弱基因信号因子进行综合整体评估后,给出IS风险预测值。

该研究检测了日本13214名IS患者与26470名正常人(无IS)的基因型(衍生数据集),用加权多位点基因风险评分系统与多基因风险评分系统分别对上述研究人员的基因型进行IS风险分析,然后,用两组独立的日本样本(KyushuU与JPJM数据集),分别评估每种评分系统的风险预测能力。

在KyushuU与JPJM数据集中,多基因风险评估系统(polyGRS)的IS风险预测结果与IS高度相关,而加权多位点基因风险评分系统的风险预测结果与IS相关性较差。KyushuU与JPJM数据集中,通过比较polyGRS五分位数的高值与低值,其IS优势比(OR)分别为1.75(95%的可信区间,1.33-2.31)与1.99(95%的可信区间,1.19-3.33)。使用KyushuU样本,将多基因风险评估系统(polyGRS)与非基因风险评估模型结合使用,极大的提高了IS风险预测能力(净重分组改善=0.151;P<0.001)

与加权多位点基因风险评分系统相比,多基因风险评分系统(polyGRS)在IS风险预测上更具优势。与非基因风险评分模型联合使用,polyGRS将为个体IS风险预测与IS可控风险因素的管控提供宝贵信息。

原始出处:

Hachiya Tsuyoshi,et al. Genetic Predisposition to Ischemic Stroke: A Polygenic Risk Score. Stroke. 2017;48:253-258.doi.org/10.1161/STROKEAHA.116.014506

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    2017-08-03 syscxl
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脑卒中幸存者及照顾者的QOL,主要受幸存者的身体功能变化的影响。在脑卒中康复的二元方法中承认幸存者及照顾者之间相互依存性是必要的。

Stroke:脑卒中患者运用依达拉奉和组织型纤溶酶原激活剂联合治疗的疗效分析!

静脉输入依达拉奉的时间并不影响组织型纤溶酶原激活剂治疗后的早期再通率、症状性脑出血或有利结局。

Stroke:磁共振成像预测急性缺血性脑卒中再灌注后脑血肿

急性缺血性卒中患者发生脑实质出血(PH)的风险增加,特别是在再灌注治疗的过程中。近期,一项发表在Stroke杂志上的研究开发了一个预测模型,模型使用组合磁共振灌注和扩散参数,包括脑血容量(CBV),表观弥散系数和微血管通透性(K2)来检查发生PH的风险。此项研究基于CBV,K2值的立体像素;使用参与MR RESCUE临床试验(使用栓子切除术的中风血栓的机械回缩和再通)的患者的预处理磁共振成像数据,

快速一览:近期脑卒中相关研究进展汇总

脑卒中是全球最主要的致死病因之一,亦是最主要的疾病负担;我国是脑卒中高发国家之一,且发病率以每年8.7%的速率上升,发病者约30%死亡,生存者亦或伴有偏瘫、失语等残障。小编整理了1月以来脑卒中亮点研究进展,与大家分享。【1】Neurology:多发脑梗死和ICAS对轻微脑卒中或TIA患者有何影响? 近日,神经病学领域权威取杂志Neurology上发表了一篇研究文章,研究人员旨在评估不