• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

先天性长QT综合征LQT1和LQT2型患者空间复极异常的检测。

Detection of spatial repolarization abnormalities in patients with LQT1 and LQT2 forms of congenital long-QT syndrome.

作者信息

Kandori Akihiko, Shimizu Wataru, Yokokawa Miki, Maruo Takeshi, Kanzaki Hideaki, Nakatani Satoshi, Kamakura Shiro, Miyatake Kunio, Murakami Masahiro, Miyashita Tsuyoshi, Ogata Kuniomi, Tsukada Keiji

机构信息

Central Research Laboratory, Hitachi Ltd, 1-280 Higashi-Koigakubo, Kokubunji, Tokyo 185-8601, Japan.

出版信息

Physiol Meas. 2002 Nov;23(4):603-14. doi: 10.1088/0967-3334/23/4/301.

DOI:10.1088/0967-3334/23/4/301
PMID:12450262
Abstract

The aim of this study is to detect the spatial current dispersion that appears in the T-wave of patients with congenital long-QT syndrome (LQTS). To observe this dispersion, magnetocardiograms (MCGs)--which have a high spatial resolution--of LQT1 patients (n = 7), LQT2 patients (n = 9) and a control group (n = 33) were recorded. The dispersion was evaluated by plotting current-arrow maps (CAMs) calculated from the MCG signals. In the case of LQT1, abnormal current arrows in the CAMs appeared above the inferior part of the heart in two LQT1 patients with a long corrected QT interval (QTc) (>0.6), and the current direction was from the left (origin side) to the right ventricular muscle (110 degrees). In six out of nine LQT2 patients, abnormal current arrows with angles below 20 degrees were observed above the right inferior part or lower septum; the current direction was from the right (origin side) to the left ventricular muscle. However, in the case of the LQT2 patients, the QTc values did not correlate with the abnormal current. These findings suggest that the origin of abnormal repolarization in LQT1 is the left ventricular muscle and the origin of that in LQT2 is the right ventricular muscle or lower septum. The estimation of the origin in LQTS patients can provide important information such as the risk factor of sudden death.

摘要

本研究的目的是检测先天性长QT综合征(LQTS)患者T波中出现的空间电流离散情况。为观察这种离散情况,记录了LQT1患者(n = 7)、LQT2患者(n = 9)和对照组(n = 33)的高空间分辨率心磁图(MCG)。通过绘制根据MCG信号计算得出的电流箭头图(CAM)来评估离散情况。在LQT1患者中,两名校正QT间期(QTc)较长(>0.6)的LQT1患者的CAM中,异常电流箭头出现在心脏下部上方,电流方向是从左侧(起始侧)指向右心室肌(110度)。在9名LQT2患者中的6名患者中,在右下部分或下间隔上方观察到角度低于20度的异常电流箭头;电流方向是从右侧(起始侧)指向左心室肌。然而,对于LQT2患者,QTc值与异常电流并无关联。这些发现表明,LQT1中异常复极化的起源是左心室肌,而LQT2中异常复极化的起源是右心室肌或下间隔。对LQTS患者起源的估计可为诸如猝死风险因素等重要信息提供依据。

相似文献

1
Detection of spatial repolarization abnormalities in patients with LQT1 and LQT2 forms of congenital long-QT syndrome.先天性长QT综合征LQT1和LQT2型患者空间复极异常的检测。
Physiol Meas. 2002 Nov;23(4):603-14. doi: 10.1088/0967-3334/23/4/301.
2
Sympathetic stimulation produces a greater increase in both transmural and spatial dispersion of repolarization in LQT1 than LQT2 forms of congenital long QT syndrome.与先天性长QT综合征的LQT2型相比,交感神经刺激在LQT1型中引起跨壁复极离散和空间复极离散的增加幅度更大。
J Am Coll Cardiol. 2001 Mar 1;37(3):911-9. doi: 10.1016/s0735-1097(00)01200-6.
3
Effect of Left Cardiac Sympathetic Denervation on the Electromechanical Window in Patients with either Type 1 or Type 2 Long QT Syndrome: A Pilot Study.左心交感神经去神经支配对1型或2型长QT综合征患者机电窗的影响:一项初步研究。
Congenit Heart Dis. 2016 Sep;11(5):437-443. doi: 10.1111/chd.12332. Epub 2016 Feb 17.
4
Architectural T-Wave Analysis and Identification of On-Therapy Breakthrough Arrhythmic Risk in Type 1 and Type 2 Long-QT Syndrome.1型和2型长QT综合征的心电图T波形态分析及治疗期间心律失常突破性风险的识别
Circ Arrhythm Electrophysiol. 2017 Nov;10(11). doi: 10.1161/CIRCEP.117.005648.
5
Differential effects of beta-blockade on dispersion of repolarization in the absence and presence of sympathetic stimulation between the LQT1 and LQT2 forms of congenital long QT syndrome.在先天性长QT综合征的LQT1和LQT2亚型中,β受体阻滞剂在有无交感神经刺激情况下对复极离散度的不同影响。
J Am Coll Cardiol. 2002 Jun 19;39(12):1984-91. doi: 10.1016/s0735-1097(02)01894-6.
6
Gene-specific effect of beta-adrenergic blockade on corrected QT interval in the long QT syndrome.β-肾上腺素能阻滞剂对长QT综合征校正QT间期的基因特异性作用。
Ann Noninvasive Electrocardiol. 2013 Jul;18(4):399-408. doi: 10.1111/anec.12048. Epub 2013 May 3.
7
Ambulatory electrocardiographic evidence of transmural dispersion of repolarization in patients with long-QT syndrome type 1 and 2.1型和2型长QT综合征患者复极跨壁离散的动态心电图证据
Circulation. 2002 Nov 5;106(19):2473-8. doi: 10.1161/01.cir.0000036369.16112.7d.
8
A quantitative assessment of T-wave morphology in LQT1, LQT2, and healthy individuals based on Holter recording technology.基于动态心电图记录技术对LQT1、LQT2患者及健康个体T波形态的定量评估。
Heart Rhythm. 2008 Jan;5(1):11-8. doi: 10.1016/j.hrthm.2007.08.026. Epub 2007 Aug 28.
9
Epinephrine QT stress testing in the evaluation of congenital long-QT syndrome: diagnostic accuracy of the paradoxical QT response.肾上腺素QT应激试验在先天性长QT综合征评估中的应用:反常QT反应的诊断准确性
Circulation. 2006 Mar 21;113(11):1385-92. doi: 10.1161/CIRCULATIONAHA.105.600445. Epub 2006 Mar 13.
10
Effect of phenylephrine provocation on dispersion of repolarization in congenital long QT syndrome.去氧肾上腺素激发试验对先天性长QT综合征复极离散度的影响。
Ann Noninvasive Electrocardiol. 2003 Jul;8(3):208-14. doi: 10.1046/j.1542-474x.2003.08307.x.

引用本文的文献

1
Standard template of adult magnetocardiogram.成人磁心动图标准模板。
Ann Noninvasive Electrocardiol. 2008 Oct;13(4):391-400. doi: 10.1111/j.1542-474X.2008.00246.x.
2
Pseudo current density maps of electrophysiological heart, nerve or brain function and their physical basis.心脏、神经或脑功能电生理的伪电流密度图及其物理基础。
Biomagn Res Technol. 2006 Oct 13;4:5. doi: 10.1186/1477-044X-4-5.
3
Visualization of three-dimensional cardiac electrical excitation using standard heart model and anterior and posterior magnetocardiogram.
使用标准心脏模型以及前后部心磁图对三维心脏电激动进行可视化。
Int J Cardiovasc Imaging. 2006 Jun-Aug;22(3-4):581-93. doi: 10.1007/s10554-005-9048-5. Epub 2006 Mar 7.
4
Identifying patterns of spatial current dispersion that characterise and separate the Brugada syndrome and complete right-bundle branch block.
Med Biol Eng Comput. 2004 Mar;42(2):236-44. doi: 10.1007/BF02344637.