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冠心病及其危险因素的双生子研究。

Twin studies of coronary heart disease and its risk factors.

作者信息

Berg K

机构信息

Institute of Medical Genetics, University of Oslo, Norway.

出版信息

Acta Genet Med Gemellol (Roma). 1987;36(4):439-53. doi: 10.1017/s0001566000006814.

Abstract

Traditional twin studies have resulted in higher concordance rates for premature coronary heart disease (CHD) in MZ than in DZ twin pairs. This is in agreement with strong evidence from several other studies, that genetic factors are of importance in the etiology of early onset CHD. Also, in a study of 291 Norwegian twin pairs the concordance rate for hypertension wa 0.36 in MZ and 0.08 in DZ pairs. Relationship between diseases and traditional gene markers have been extensively studied and several associations have been uncovered for CHD. Our group has developed a method to examine a possible permissive or restrictive effect of single genes on the degree of variation that environmental and/or life style factors can cause in a given parameter. This method for studying gene-environment interaction is based on the fact that MZ twins are identical with respect to genes, so that any difference between the two members of an MZ pair must necessarily be caused by environmental or life style factors. The possibility that a given gene influences the degree of variability in a parameter such as cholesterol is examined by comparing the within-pair difference in cholesterol level between MZ pairs possessing, and MZ pairs lacking the gene in question, and results of such studies will be presented. New possibilities to study restriction fragment length polymorphisms (RFLPs) at apolipoprotein loci have added a new dimension to research on genetics of CHD and hyperlipidemias. Association between apolipoprotein B, cholesterol and fasting triglyceride levels on one hand and DNA variation at the apolipoprotein B locus on the other has been found.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

传统的双胞胎研究结果显示,同卵双胞胎(MZ)中早发性冠心病(CHD)的一致率高于异卵双胞胎(DZ)。这与其他几项研究的有力证据相符,即遗传因素在早发性冠心病的病因中具有重要作用。此外,在一项对291对挪威双胞胎的研究中,高血压的一致率在同卵双胞胎中为0.36,在异卵双胞胎中为0.08。疾病与传统基因标记之间的关系已得到广泛研究,并且已经发现了一些与冠心病相关的关联。我们小组开发了一种方法,以研究单个基因对环境和/或生活方式因素在给定参数中可能引起的变异程度的许可或限制作用。这种研究基因-环境相互作用的方法基于这样一个事实,即同卵双胞胎在基因方面是相同的,因此同卵双胞胎对中两个成员之间的任何差异必然是由环境或生活方式因素引起的。通过比较拥有和缺乏相关基因的同卵双胞胎对之间胆固醇水平的配对内差异,来检验给定基因对胆固醇等参数变异程度的影响,此类研究结果将予以呈现。研究载脂蛋白基因座处限制性片段长度多态性(RFLP)的新方法为冠心病和高脂血症的遗传学研究增添了新的维度。一方面发现了载脂蛋白B、胆固醇和空腹甘油三酯水平之间的关联,另一方面发现了载脂蛋白B基因座处的DNA变异。(摘要截选至250字)

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