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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.与遗传性 J 波综合征和心源性猝死相关的心脏 L 型钙通道突变。
Heart Rhythm. 2010 Dec;7(12):1872-82. doi: 10.1016/j.hrthm.2010.08.026. Epub 2010 Oct 14.
2
Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).心电图早期复极模式与心脏和全因死亡率的关系:一项基于人群的前瞻性队列研究(MONICA/KORA)。
PLoS Med. 2010 Jul 27;7(7):e1000314. doi: 10.1371/journal.pmed.1000314.
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Normal variations in multiple precordial leads.多个心前区导联的正常变异
Am Heart J. 1947 Dec;34(6):785-808. doi: 10.1016/0002-8703(47)90144-0.
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J wave syndromes.J 波综合征。
Heart Rhythm. 2010 Apr;7(4):549-58. doi: 10.1016/j.hrthm.2009.12.006. Epub 2009 Dec 11.
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Long-term outcome associated with early repolarization on electrocardiography.心电图早期复极与长期预后的关系。
N Engl J Med. 2009 Dec 24;361(26):2529-37. doi: 10.1056/NEJMoa0907589. Epub 2009 Nov 16.
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Common variants at ten loci influence QT interval duration in the QTGEN Study.在QTGEN研究中,十个基因座上的常见变异影响QT间期持续时间。
Nat Genet. 2009 Apr;41(4):399-406. doi: 10.1038/ng.364. Epub 2009 Mar 22.
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Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.一氧化氮合酶1衔接蛋白的基因变异与美国白人社区人群的心源性猝死相关。
Circulation. 2009 Feb 24;119(7):940-51. doi: 10.1161/CIRCULATIONAHA.108.791723. Epub 2009 Feb 9.
8
Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study.冠心病患者QT间期延长的决定因素及其对猝死风险的影响:俄勒冈州意外猝死研究
Circulation. 2009 Feb 10;119(5):663-70. doi: 10.1161/CIRCULATIONAHA.108.797035. Epub 2009 Jan 26.
9
Electrocardiographic (ECG) criteria for determining left ventricular mass in young healthy men; data from the LARGE Heart study.用于确定年轻健康男性左心室质量的心电图(ECG)标准;来自“大心脏”研究的数据。
J Cardiovasc Magn Reson. 2009 Jan 16;11(1):2. doi: 10.1186/1532-429X-11-2.
10
Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel.室颤伴显著早期复极,与KCNJ8/KATP通道的一种罕见变异相关。
J Cardiovasc Electrophysiol. 2009 Jan;20(1):93-8. doi: 10.1111/j.1540-8167.2008.01326.x.

一般人群中的早期复极模式:临床相关性和遗传性。

The early repolarization pattern in the general population: clinical correlates and heritability.

机构信息

Cardiovascular Research Center and Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA.

出版信息

J Am Coll Cardiol. 2011 May 31;57(22):2284-9. doi: 10.1016/j.jacc.2011.04.003.

DOI:10.1016/j.jacc.2011.04.003
PMID:21600720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3183435/
Abstract

OBJECTIVES

This study sought to describe the clinical correlates and heritability of the early repolarization pattern (ERP) in 2 large, population-based cohorts.

BACKGROUND

There is growing recognition that ERP is associated with adverse outcomes.

METHODS

Participants of the Framingham Heart Study (FHS) (N = 3,995) and the Health 2000 Survey (H2K) (N = 5,489) were included. ERP was defined as a J-point elevation ≥0.1 mV in ≥2 leads in either the inferior (II, III, aVF) or lateral (I, aVL, V(4-6)) territory or both. We tested the association between clinical characteristics and ERP, and estimated sibling recurrence risk.

RESULTS

ERP was present in 243 of 3,955 (6.1%) of FHS and 180 of 5,489 (3.3%) of H2K subjects. Male sex, younger age, lower systolic blood pressure, higher Sokolow-Lyon index, and lower Cornell voltage were independently associated with the presence of ERP. In the FHS sample, siblings of individuals with ERP had an ERP prevalence of 11.6% (recurrence risk ratio of 1.89). Siblings of individuals with ERP had an increased unadjusted odds of ERP (odds ratio: 2.22, 95% confidence interval: 1.01 to 4.85, p = 0.047).

CONCLUSIONS

ERP has strong association with clinical factors and has evidence for a heritable basis in the general population. Further assessment of the genetic determinants of ERP is warranted.

摘要

目的

本研究旨在描述 2 个大型人群队列中早期复极(ERP)的临床相关性和遗传性。

背景

越来越多的人认识到 ERP 与不良结局相关。

方法

纳入弗雷明汉心脏研究(FHS)(N=3995)和健康 2000 调查(H2K)(N=5489)的参与者。ERP 定义为在下壁(II、III、aVF)或侧壁(I、aVL、V(4-6))或两者中至少 2 个导联 J 点抬高≥0.1 mV。我们检验了临床特征与 ERP 的相关性,并估计了同胞复发风险。

结果

FHS 中 3955 例(6.1%)和 H2K 中 5489 例(3.3%)存在 ERP。男性、年龄较小、收缩压较低、Sokolow-Lyon 指数较高和 Cornell 电压较低与 ERP 的存在独立相关。在 FHS 样本中,ERP 个体的同胞 ERP 患病率为 11.6%(复发风险比为 1.89)。ERP 个体的同胞在未经调整的 ERP 发生比值比方面具有较高的优势(比值比:2.22,95%置信区间:1.01 至 4.85,p=0.047)。

结论

ERP 与临床因素密切相关,并且在普通人群中具有遗传性基础。进一步评估 ERP 的遗传决定因素是必要的。