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Stroke. 2011 Nov;42(11):3017-21. doi: 10.1161/STROKEAHA.111.625186. Epub 2011 Sep 1.
2
Complement C3 and cleavage products in cardiometabolic risk.补体 C3 及其代谢产物与心脏代谢风险。
Clin Chim Acta. 2011 Jun 11;412(13-14):1171-9. doi: 10.1016/j.cca.2011.03.005. Epub 2011 Mar 15.
3
The value of carotid intima-media thickness for predicting cardiovascular risk.颈动脉内膜中层厚度预测心血管风险的价值。
Arterioscler Thromb Vasc Biol. 2010 Feb;30(2):182-5. doi: 10.1161/ATVBAHA.109.196980. Epub 2009 Nov 30.
4
Noninvasive assessment of subclinical atherosclerosis in children and adolescents: recommendations for standard assessment for clinical research: a scientific statement from the American Heart Association.儿童和青少年亚临床动脉粥样硬化的无创评估:临床研究标准评估建议:美国心脏协会科学声明
Hypertension. 2009 Nov;54(5):919-50. doi: 10.1161/HYPERTENSIONAHA.109.192639. Epub 2009 Sep 3.
5
The 1425G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population.蛋白激酶C eta型基因(PRKCH)中的1425G/A单核苷酸多态性与中国人群的缺血性中风和脑出血有关。
Stroke. 2009 Sep;40(9):2973-6. doi: 10.1161/STROKEAHA.109.551747. Epub 2009 Jun 11.
6
Ultrasound imaging techniques for the evaluation of cardiovascular therapies.用于评估心血管治疗的超声成像技术。
Eur Heart J. 2008 Apr;29(7):849-58. doi: 10.1093/eurheartj/ehn070. Epub 2008 Mar 11.
7
Association between PRKCH gene polymorphisms and subcortical silent brain infarction.PRKCH基因多态性与皮质下无症状性脑梗死之间的关联。
Atherosclerosis. 2008 Aug;199(2):340-5. doi: 10.1016/j.atherosclerosis.2007.11.009. Epub 2007 Dec 31.
8
A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.蛋白激酶Cη(PRKCH)基因中的一个非同义单核苷酸多态性增加了脑梗死的风险。
Nat Genet. 2007 Feb;39(2):212-7. doi: 10.1038/ng1945. Epub 2007 Jan 7.
9
Effects of C-reactive protein and the third and fourth components of complement (C3 and C4) on incidence of atrial fibrillation.C反应蛋白及补体第三和第四成分(C3和C4)对心房颤动发生率的影响。
Am J Cardiol. 2006 Jan 15;97(2):245-8. doi: 10.1016/j.amjcard.2005.08.027. Epub 2005 Nov 28.
10
Carotid intima-media thickening indicates a higher vascular risk across a wide age range: prospective data from the Carotid Atherosclerosis Progression Study (CAPS).颈动脉内膜中层增厚表明在广泛年龄范围内存在较高的血管风险:来自颈动脉粥样硬化进展研究(CAPS)的前瞻性数据。
Stroke. 2006 Jan;37(1):87-92. doi: 10.1161/01.STR.0000196964.24024.ea. Epub 2005 Dec 8.

SNP(rs2230500)在 PRKCH 中降低了中国年轻成年人颈动脉内膜中层厚度的风险。

The SNP (rs2230500) in PRKCH decreases the risk of carotid intima-media thickness in a Chinese young adult population.

机构信息

Department of Epidemiology, Capital Institute of Pediatrics, Beijing, China.

出版信息

PLoS One. 2012;7(7):e40606. doi: 10.1371/journal.pone.0040606. Epub 2012 Jul 11.

DOI:10.1371/journal.pone.0040606
PMID:22808203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3394745/
Abstract

BACKGROUND

The SNP (rs2230500) in PRKCH (the gene encoding protein kinase C η) is associated with ischemic stroke and cerebral hemorrhage in the Chinese population, but the molecular mechanisms are not clear. The aim of the present study is to investigate the association between the SNP and atherosclerosis that is common pathological basis of ischemic stroke and cerebral hemorrhage.

METHODOLOGY/PRINCIPAL FINDINGS: We examined the associations of the SNP with carotid intima-media thickness (CIMT), atherosclerosis diagnosed by CIMT, and factors related with inflammation in the Beijing Child Blood Pressure Study. A total of 1190 subjects participated in the follow-up study. The SNP was genotyped by allele-specific real-time PCR assay. The SNP (rs2230500) in PRKCH was significantly associated with CIMT (in far wall of left common carotid arteries, P = 0.016; in far wall of right common carotid arteries, P = 0.012) under a recessive model after adjustment for age, gender, smoking, and hypertension. The SNP was also significantly associated with complement C3 (P = 0.012) under a dominant model after adjustment for age, gender, and high sensitivity C-reactive protein.

CONCLUSIONS/SIGNIFICANCE: Our data provide evidence that the SNP (rs2230500) in PRKCH decreases the risk of CIMT that is a worthwhile predictor of stroke and complement system possibly mediates this process.

摘要

背景

SNP(rs2230500)位于 PRKCH(蛋白激酶 C η 基因),与中国人群的缺血性卒中和脑出血有关,但分子机制尚不清楚。本研究旨在探讨 SNP 与动脉粥样硬化的关系,动脉粥样硬化是缺血性卒中和脑出血的共同病理基础。

方法/主要发现:我们通过颈动脉内膜中层厚度(CIMT)检查,研究 SNP 与动脉粥样硬化的关系,CIMT 用于诊断动脉粥样硬化,以及与炎症相关的因素与北京儿童血压研究有关。共有 1190 名受试者参加了随访研究。采用等位基因特异性实时 PCR 检测 SNP。PRKCH 中的 SNP(rs2230500)在调整年龄、性别、吸烟和高血压后,在隐性模型下与 CIMT(左颈总动脉远壁,P=0.016;右颈总动脉远壁,P=0.012)显著相关。调整年龄、性别和高敏 C 反应蛋白后,SNP 也在显性模型下与补体 C3(P=0.012)显著相关。

结论/意义:我们的数据提供了证据,表明 PRKCH 中的 SNP(rs2230500)降低了 CIMT 的风险,CIMT 是中风的一个有价值的预测指标,补体系统可能介导了这一过程。