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本文引用的文献

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A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study.一项针对1933个受早发性冠状动脉疾病影响家庭的全基因组连锁研究:英国心脏基金会(BHF)家庭心脏研究。
Am J Hum Genet. 2005 Dec;77(6):1011-20. doi: 10.1086/498653. Epub 2005 Oct 25.
2
Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions.脂质参数四项新基因组扫描的荟萃分析及阳性连锁区域位置候选基因分析。
Eur J Hum Genet. 2005 Oct;13(10):1143-53. doi: 10.1038/sj.ejhg.5201466.
3
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.对438个家庭进行的早发性冠状动脉疾病全基因组扫描:GENECARD研究。
Am J Hum Genet. 2004 Sep;75(3):436-47. doi: 10.1086/423900. Epub 2004 Jul 22.
4
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.编码5-脂氧合酶激活蛋白的基因会增加心肌梗死和中风的风险。
Nat Genet. 2004 Mar;36(3):233-9. doi: 10.1038/ng1311. Epub 2004 Feb 8.
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Mutation of MEF2A in an inherited disorder with features of coronary artery disease.在一种具有冠状动脉疾病特征的遗传性疾病中MEF2A的突变
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Welcome to the genomic era.欢迎来到基因组时代。
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Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.急性冠状动脉综合征的全基因组连锁分析表明2号染色体上存在一个基因座。
Arterioscler Thromb Vasc Biol. 2002 May 1;22(5):874-8. doi: 10.1161/01.atv.0000016258.40568.f1.
8
A comprehensive linkage analysis for myocardial infarction and its related risk factors.心肌梗死及其相关危险因素的综合连锁分析。
Nat Genet. 2002 Feb;30(2):210-4. doi: 10.1038/ng827. Epub 2002 Jan 30.
9
Lipoproteins, nutrition, and heart disease.脂蛋白、营养与心脏病
Am J Clin Nutr. 2002 Feb;75(2):191-212. doi: 10.1093/ajcn/75.2.191.
10
Simple scoring scheme for calculating the risk of acute coronary events based on the 10-year follow-up of the prospective cardiovascular Münster (PROCAM) study.基于前瞻性心血管明斯特(PROCAM)研究10年随访结果计算急性冠脉事件风险的简易评分方案。
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基因、饮食与公共健康。

Genes, diet and public health.

机构信息

Leibniz Institute for Arteriosclerosis Research, University of Munster, 49149, Munster, Germany,

出版信息

Genes Nutr. 2007 Oct;2(1):75-80. doi: 10.1007/s12263-007-0001-1.

DOI:10.1007/s12263-007-0001-1
PMID:18850146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2474917/
Abstract

Common chronic diseases such as coronary heart disease (CHD), diabetes, cancer, hypertension and obesity are significantly influenced by dietary and other behavioural habits. There is increasing scientific evidence that genetic factors (SNPs), conferring either protection or risk, also contribute importantly to the incidence of these diseases. SNPs are of particular interest because they influence disease in a complex but largely unknown manner by interacting with environmental and lifestyle factors. Because genetic factors also affect a person's response to dietary habits, SNPs likely will be useful in helping to determine and understand why individuals differ in their response to diets. Therefore, the discovery of SNPs will likely revolutionize not only the diagnosis of disease but also the practice of preventative medicine. Other developments, like new biomarkers and noninvasive imaging techniques, might turn out to be highly sensitive and specific in order to identify patients at risk, especially in cases with asymptomatic coronary heart disease. Thus, further knowledge of such new risk factors and their interaction with nutrition, has the potential to provide a more precise and personalized approach to prevent and treat chronic diseases like coronary artery disease, myocardial infarction and stroke.

摘要

常见的慢性病,如冠心病(CHD)、糖尿病、癌症、高血压和肥胖症,明显受到饮食和其他行为习惯的影响。越来越多的科学证据表明,遗传因素(单核苷酸多态性,SNP),无论是保护还是风险,也对这些疾病的发病率有重要贡献。SNP 特别有趣,因为它们通过与环境和生活方式因素相互作用,以复杂但在很大程度上未知的方式影响疾病。由于遗传因素也会影响一个人对饮食习惯的反应,因此 SNP 可能有助于确定和理解为什么个体对饮食的反应不同。因此,SNP 的发现不仅可能彻底改变疾病的诊断,而且可能彻底改变预防医学的实践。其他发展,如新的生物标志物和非侵入性成像技术,可能会非常敏感和特异,以便识别有风险的患者,特别是在无症状性冠心病的情况下。因此,进一步了解这些新的危险因素及其与营养的相互作用,有可能为预防和治疗冠心病、心肌梗死和中风等慢性疾病提供更精确和个性化的方法。