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冠心病:遗传学方面

Coronary heart disease: genetic aspects.

作者信息

Neufeld H N, Goldbourt U

出版信息

Circulation. 1983 May;67(5):943-54. doi: 10.1161/01.cir.67.5.943.

Abstract

Morbidity and mortality differences between populations, between ethnic groups and between individuals are not satisfactorily explained by the variation of risk factors. Differences in genetic susceptibility might be responsible for a part of the unexplained variation of coronary heart disease (CHD) rates. Genetic factors are also significant in determining the level of risk factors in individuals. Ample evidence links genetic factors to the levels of serum cholesterol, blood pressure and diabetes. Marked sex differences in CHD mortality also indicate the role of heredity in the development of the disease. The male:female ratio varies widely between different countries, as well as between different ethnic groups. These variations are difficult to explain by variation in environmental and behavioral differences between males and females alone. The degree of atherosclerosis in males and females varies, depending on the anatomic location of the atherosclerosis. Inherited disorders of metabolism and the variability of anatomic patterns provide additional indications of the role of genetics. The data accumulated in the Israeli Ischemic Heart Disease Study over 15 years reveal an ethnic variation of risk factors coupled with remarkably larger variation in disease rates. Patterns of incidence assessed in the national mortality data of the Israeli study and in histologic findings in the coronary arteries of infants from different ethnic groups are compatible with a hypothesis that ethnic and sex differences in early structural changes of the coronary arteries partly determine the susceptibility of the latter to the development of atherosclerosis. In conclusion, findings from our studies and the review of the evidence from genetic epidemiologic investigations indicate a significant role of genetics in determining the degree, time course and severity of the atherosclerotic process and of the occurrence of symptomatic CHD. This important role of the genetic component is relevant to preventive strategies offered as tools for reducing the burden of CHD. Research into genetic determinants of both susceptibility to atherosclerosis or clinical manifestation of CHD and individual response to preventive measures should be encouraged.

摘要

人群之间、种族群体之间以及个体之间的发病率和死亡率差异,无法通过风险因素的变化得到令人满意的解释。遗传易感性的差异可能是冠心病(CHD)发病率中部分无法解释的变化的原因。遗传因素在决定个体的风险因素水平方面也很重要。大量证据将遗传因素与血清胆固醇水平、血压和糖尿病联系起来。冠心病死亡率中明显的性别差异也表明遗传在该疾病发展中的作用。男性与女性的比例在不同国家以及不同种族群体之间差异很大。仅靠男性和女性在环境和行为方面的差异变化很难解释这些差异。男性和女性的动脉粥样硬化程度因动脉粥样硬化的解剖位置而异。遗传性代谢紊乱和解剖模式的变异性进一步表明了遗传的作用。以色列缺血性心脏病研究15年来积累的数据显示,风险因素存在种族差异,同时疾病发病率的差异明显更大。在以色列研究的全国死亡率数据中评估的发病率模式以及不同种族婴儿冠状动脉的组织学发现与以下假设相符:冠状动脉早期结构变化中的种族和性别差异部分决定了后者对动脉粥样硬化发展的易感性。总之,我们的研究结果以及对遗传流行病学调查证据的回顾表明,遗传在决定动脉粥样硬化过程的程度、时间进程和严重程度以及有症状冠心病的发生方面起着重要作用。遗传因素的这一重要作用与作为减轻冠心病负担工具的预防策略相关。应鼓励对动脉粥样硬化易感性或冠心病临床表现的遗传决定因素以及个体对预防措施的反应进行研究。

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