The significance of ACE gene polymorphism in ischemic heart disease
ACE基因多态性在缺血性心脏病中的意义
基本信息
- 批准号:07670801
- 负责人:
- 金额:$ 1.41万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1995
- 资助国家:日本
- 起止时间:1995 至 1996
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
A difference with a Japanese and Westerners in a relation with a myocardial infarction (MI) and an angiotensin converting enzyme (ACE) gene polymorphism has not been fully elucidated. And a research in a Japanese with regard to relation between ACE gene polymorphism and the left ventricular remodeling after a MI are needed. We examined the significance of ACE gene polymorphism in the prognosis and the generation of left ventricular late potentials in healthy control and MI patients.An ACE gene polymorphism was determined with PCR method in gathering DNA from a leukocyte. A presence of ventricular late potential was determined with an signal-averaged electrocardiogram. Also, a questionnaire survey by a letter was carried out. We analyzed a relation between ACE gene polymorphism and the presence of a cardiac events with Kaplan-Meier, and also analyzed the relation to left ventricular late potentials after the first MI.[Results]1) ACE gene DD genotype could become a new coronary risk factor even Japanese ischemic heart disease (Circulation, 1995). 2) Total frequencies of cardiac events in low risk group (TC<260mg/dl, HbAlc<9.0%, BMI<26) after the first MI was 7 from 34 MI cases with ACE II genotype (20.6%), 15 from 71 MI cases with ACE ID genotype (21.1%), 21 from 58 MI cases with ACE DD genotype (36.2%). Kaplan-Meier analysis revealed that cardiac events in MI patients with ACE DD genotype were tendency to be increased than those in MI patients with ACE II and ID genotype (Musya T,Nakai K : J Iwate Med, 1997.in print). 3) A positive left ventricular late potentials increased the incidence in MI patients with an ACE DD genotype (Nakai K et al : A.N.E.1 : 405-410,1996).We concluded that ACE DD genotype might relate to the genesis of cardiac events and left ventricular remodeling after the first MI in the Japanese.
日本人和西方人在心肌梗塞(MI)与血管紧张素转换酶(ACE)基因多态性的关系上的差异尚未完全阐明。还需要在日本人中进行关于ACE基因多态性与MI后左心室重构之间关系的研究。本研究采用PCR方法检测ACE基因多态性,并与正常对照组和心肌梗死患者进行比较,探讨ACE基因多态性与心肌梗死患者预后及左心室晚电位的关系。通过信号平均心电图确定心室晚电位的存在。此外,还通过信函进行了问卷调查。采用Kaplan-Meier法分析ACE基因多态性与心脏事件发生的关系,并分析ACE基因多态性与首次MI后左心室晚电位的关系。[结果]1)ACE基因DD基因型可能成为新的冠心病危险因素,甚至在日本人中也可能成为缺血性心脏病的危险因素(Circulation,1995)。2)低危组(TC<260 mg/dl,HbAlc<9.0%,BMI<26)首次心肌梗死后心脏事件发生率分别为:ACE Ⅱ型34例中7例(20.6%),ACE ID型71例中15例(21.1%),ACE DD型58例中21例(36.2%)。Kaplan-Meier分析显示,ACE DD基因型MI患者的心脏事件比ACE II和ID基因型MI患者的心脏事件有增加的趋势(Musya T,Nakai K:J Iwate Med,1997.in print)。3)左心室晚电位阳性增加了ACE DD基因型心肌梗死患者的发病率(Nakai K et al:A.N.E.1:405- 410,1996),我们的结论是ACE DD基因型可能与日本人首次心肌梗死后心脏事件的发生和左心室重构有关。
项目成果
期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Nakai K,et al.: "Deletion polymorphism of the angiotensin I-converting enzyme gene associates with increased risk for late potentials in patients with myocardial infarction." A.N.E. 1. 405-410 (1996)
Nakai K 等人:“血管紧张素 I 转换酶基因的缺失多态性与心肌梗塞患者晚期电位风险增加相关。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Nakai K, et al: "Delection polymorphisim of the angiotensin I-converting enzyme gene associated with increased for late potential in myocardial infarction" Circulation. 92. I-741-I-742 (1995)
Nakai K 等人:“血管紧张素 I 转换酶基因的缺失多态性与心肌梗塞晚期电位增加相关”循环。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
武者毅彦、中居賢司: "急性心筋梗塞症の発症と予後に関わるアンジオテンシン-I変換酵素遺伝子型の解析" 岩手医誌. (掲載予定). (1997)
Takehiko Musha,Kenji Nakai:“与急性心肌梗塞的发病和预后相关的血管紧张素-I转换酶基因型分析”岩手医学杂志(待出版)。
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- 影响因子:0
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NAKAI Kenji其他文献
NAKAI Kenji的其他文献
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{{ truncateString('NAKAI Kenji', 18)}}的其他基金
Development of software system for next-generation multi-channel high amplification and high resolution ECG and clinical application
新一代多通道高放大高分辨率心电图软件系统开发及临床应用
- 批准号:
22590792 - 财政年份:2010
- 资助金额:
$ 1.41万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Determination of Impact Indentation Hardness for Metallic Materials and Impact Fracture Toughness for Brittle Materials
金属材料冲击压痕硬度和脆性材料冲击断裂韧性的测定
- 批准号:
21760563 - 财政年份:2009
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$ 1.41万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Early screening of myocardial injury and lethal arrhythmia by 64-channel magnetocardiography and genetical predisposition
64道心磁图及遗传易感性早期筛查心肌损伤和致死性心律失常
- 批准号:
18500383 - 财政年份:2006
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$ 1.41万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
A development of oligonucleotide based DNA array for CYP2C9 genotyping for individual therapy in patients with valve replacement receiving warfarin therapy
开发基于寡核苷酸的 DNA 阵列,用于 CYP2C9 基因分型,用于接受华法林治疗的瓣膜置换术患者的个体化治疗
- 批准号:
15590768 - 财政年份:2003
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$ 1.41万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Evaluation of genetical factor in the Japanese is chemic heart disease
日本人化学性心脏病遗传因素评价
- 批准号:
09670743 - 财政年份:1997
- 资助金额:
$ 1.41万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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