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缺血性脑卒中的基因谱。

Genetic profiles in ischaemic stroke.

机构信息

Stroke and Dementia Research Centre, St George's, University of London, Cranmer Terrace, Tooting, London, SW17 0RE, UK.

出版信息

Curr Atheroscler Rep. 2013 Aug;15(8):342. doi: 10.1007/s11883-013-0342-8.

DOI:10.1007/s11883-013-0342-8
PMID:23780749
Abstract

Stroke represents a clinical syndrome rather than a single disease. A number of stroke subtypes can be distinguished based on careful phenotyping, with each of these having distinct and overlapping risk factor profiles. Recent evidence has suggested that genetics plays an important part in stroke risk, with at least 2 genes specific to stroke risk directly now having been identified. This review will explore our current understanding of the genetics underlying stroke risk and whether this information is currently useful in a clinical setting for patient benefit.

摘要

中风是一种临床综合征,而不是一种单一的疾病。可以根据仔细的表型分析来区分许多中风亚型,其中每一种都有不同但又有重叠的危险因素特征。最近的证据表明,遗传在中风风险中起着重要作用,至少有 2 个专门针对中风风险的基因已经被直接确定。这篇综述将探讨我们对中风风险遗传基础的现有认识,以及这些信息在临床环境中是否对患者有益。

相似文献

1
Genetic profiles in ischaemic stroke.缺血性脑卒中的基因谱。
Curr Atheroscler Rep. 2013 Aug;15(8):342. doi: 10.1007/s11883-013-0342-8.
2
The genetics of stroke.中风的遗传学
Curr Opin Lipidol. 2005 Apr;16(2):193-9. doi: 10.1097/01.mol.0000162324.85290.ac.
3
Mechanisms and treatment of ischaemic stroke--insights from genetic associations.缺血性脑卒中的发病机制与治疗——遗传关联的启示。
Nat Rev Neurol. 2014 Dec;10(12):723-30. doi: 10.1038/nrneurol.2014.196. Epub 2014 Oct 28.
4
Genetics of ischaemic stroke.缺血性中风的遗传学。
J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1302-8. doi: 10.1136/jnnp-2012-304834. Epub 2013 Apr 25.
5
Genetics of ischemic stroke: future clinical applications.缺血性中风的遗传学:未来的临床应用
Semin Neurol. 2006 Nov;26(5):523-30. doi: 10.1055/s-2006-951625.
6
Genetic susceptibility and ischaemic stroke.遗传易感性与缺血性中风
Curr Opin Neurol. 1999 Feb;12(1):47-55. doi: 10.1097/00019052-199902000-00009.
7
Genetics and ischaemic stroke.遗传学与缺血性中风。
Brain. 2000 Sep;123 ( Pt 9):1784-812. doi: 10.1093/brain/123.9.1784.
8
Genetics of ischaemic stroke; single gene disorders.缺血性中风的遗传学;单基因疾病
Int J Stroke. 2006 Aug;1(3):131-9. doi: 10.1111/j.1747-4949.2006.00037.x.
9
New information on the genetics of stroke.中风遗传学的新信息。
Curr Neurol Neurosci Rep. 2011 Feb;11(1):35-41. doi: 10.1007/s11910-010-0155-x.
10
Genome-Wide Studies in Ischaemic Stroke: Are Genetics Only Useful for Finding Genes?全基因组研究在缺血性脑卒中中的应用:遗传学仅有助于发现基因吗?
Int J Mol Sci. 2022 Jun 20;23(12):6840. doi: 10.3390/ijms23126840.

引用本文的文献

1
Single-Nucleotide Polymorphisms in Oxidative Stress-Related Genes and the Risk of a Stroke in a Polish Population-A Preliminary Study.波兰人群中氧化应激相关基因的单核苷酸多态性与中风风险——一项初步研究
Brain Sci. 2021 Mar 19;11(3):391. doi: 10.3390/brainsci11030391.
2
CYP3A4 and CYP11A1 variants are risk factors for ischemic stroke: a case control study.CYP3A4 和 CYP11A1 变异是缺血性脑卒中的危险因素:一项病例对照研究。
BMC Neurol. 2020 Mar 4;20(1):77. doi: 10.1186/s12883-020-1628-4.
3
Pathogenic variants in the ABCC6 gene are associated with an increased risk for ischemic stroke.

本文引用的文献

1
Evidence HDAC9 genetic variant associated with ischemic stroke increases risk via promoting carotid atherosclerosis.证据表明,与缺血性脑卒中相关的 HDAC9 遗传变异通过促进颈动脉粥样硬化增加了风险。
Stroke. 2013 May;44(5):1220-5. doi: 10.1161/STROKEAHA.111.000217. Epub 2013 Feb 28.
2
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.缺血性中风与 ABO 基因座相关:EuroCLOT 研究。
Ann Neurol. 2013 Jan;73(1):16-31. doi: 10.1002/ana.23838.
3
Risk factors for intracerebral hemorrhage differ according to hemorrhage location.
ABCC6 基因中的致病性变异与缺血性卒中风险增加相关。
Brain Pathol. 2018 Nov;28(6):822-831. doi: 10.1111/bpa.12620.
4
A Decrease of Brain MicroRNA-122 Level Is an Early Marker of Cerebrovascular Disease in the Stroke-Prone Spontaneously Hypertensive Rat.脑微小RNA-122水平降低是易卒中自发性高血压大鼠脑血管疾病的早期标志物。
Oxid Med Cell Longev. 2017;2017:1206420. doi: 10.1155/2017/1206420. Epub 2017 Jun 18.
5
Endothelial cells and human cerebral small vessel disease.内皮细胞与人类脑小血管疾病
Brain Pathol. 2015 Jan;25(1):44-50. doi: 10.1111/bpa.12224.
脑出血的风险因素因出血部位而异。
Neurology. 2012 Dec 4;79(23):2275-82. doi: 10.1212/WNL.0b013e318276896f. Epub 2012 Nov 21.
4
Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations.遗传性缺血性脑卒中及既往报道候选基因和全基因组关联研究的贡献。
Stroke. 2012 Dec;43(12):3161-7. doi: 10.1161/STROKEAHA.112.665760. Epub 2012 Oct 4.
5
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.缺血性卒中及其亚型的遗传风险因素(METASTROKE 协作研究):全基因组关联研究的荟萃分析。
Lancet Neurol. 2012 Nov;11(11):951-62. doi: 10.1016/S1474-4422(12)70234-X. Epub 2012 Oct 5.
6
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.6p21.1 常见变异与大动脉粥样硬化性卒中相关。
Nat Genet. 2012 Oct;44(10):1147-51. doi: 10.1038/ng.2397. Epub 2012 Sep 2.
7
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.全基因组关联研究鉴定出 HDAC9 中的一个变体与大动脉粥样硬化性缺血性卒中相关。
Nat Genet. 2012 Feb 5;44(3):328-33. doi: 10.1038/ng.1081.
8
Heart disease and stroke statistics--2012 update: a report from the American Heart Association.《2012年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2012 Jan 3;125(1):e2-e220. doi: 10.1161/CIR.0b013e31823ac046. Epub 2011 Dec 15.
9
Testing should not be done in all patients treated with clopidogrel who are undergoing percutaneous coronary intervention.对于所有接受氯吡格雷治疗且正在接受经皮冠状动脉介入治疗的患者,不应进行检测。
Circ Cardiovasc Interv. 2011 Oct 1;4(5):514-21; discussion 521. doi: 10.1161/CIRCINTERVENTIONS.111.962142.
10
Current evidence for genetic testing in clopidogrel-treated patients undergoing coronary stenting.氯吡格雷治疗的冠状动脉支架置入患者基因检测的现有证据。
Circ Cardiovasc Interv. 2011 Oct 1;4(5):505-13; discussion 513. doi: 10.1161/CIRCINTERVENTIONS.111.962183.