Literature DB >> 6442089

Twin studies of coronary heart disease and its risk factors.

K Berg.   

Abstract

The ongoing comprehensive study of the updated population-based Norwegian Twin Panel (like-sexed twin pairs born since 1915) has already given results of interest to the research on coronary heart disease and its risk factors. Significantly more dizygotic (DZ) than monozygotic (MZ) pairs are discordant for death between 40 and 60 years of age. Presumably, several of the cases must have been coronary heart disease deaths. In pairs where both members are alive, concordance rate for coronary heart disease before the age of 60 years is significantly higher in MZ than in DZ pairs. Concordance rate for reported hypertension is significantly higher in MZ than in DZ pairs. These findings are compatible with a significant genetic effect on premature death, coronary heart disease and hypertension. There is a strong genetic effect on serum level of apoB, apoA-I and apoA-II, a weaker effect on cholesterol level and a doubtful effect on triglyceride level. Genes belonging to several normal genetic polymorphisms may participate in the control of environmentally/dietary caused variability in lipid and lipoprotein parameters. The study of MZ twins that was conducted to detect these effects holds considerable promise for the detection of gene control of many kinds of quantitative parameters. Further work with this twin panel may provide more definite answers to several questions raised during the present investigation. Application of more sophisticated models for twin family analysis on several normal and pathological traits may be very informative. Also, this updated Norwegian Twin Panel should in the long run make it possible to estimate the predictive value for the second member of a twin pair of having a twin contracting coronary heart disease (or any other reasonably frequent disease) by a given age. Finally, the subsample that is subjected to extensive laboratory analyses will provide useful data for genetic linkage analyses since in many cases, offspring of two members of a MZ pair can effectively be considered as one single (more informative) sibship.

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Year:  1984        PMID: 6442089     DOI: 10.1017/s0001566000005808

Source DB:  PubMed          Journal:  Acta Genet Med Gemellol (Roma)        ISSN: 0001-5660


  11 in total

1.  Pedigree and sib-pair linkage analysis suggest the apolipoprotein B gene is not the major gene influencing plasma apolipoprotein B levels.

Authors:  J Coresh; T H Beaty; P O Kwiterovich; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  The genetic aspects of atherosclerosis and hyperlipidemia.

Authors:  M R Hayden
Journal:  CMAJ       Date:  1989-07-15       Impact factor: 8.262

3.  Genetic analysis of apolipoprotein A-I in two dietary environments.

Authors:  J Blangero; J W MacCluer; C M Kammerer; G E Mott; T D Dyer; H C McGill
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

4.  Recruitment bias in twin research: the rule of two-thirds reconsidered.

Authors:  D T Lykken; M McGue; A Tellegen
Journal:  Behav Genet       Date:  1987-07       Impact factor: 2.805

5.  Linkage disequilibrium analyses and restriction mapping of four RFLPs at the pro alpha 2(I) collagen locus: lack of correlation between linkage disequilibrium and physical distance.

Authors:  A L Børresen; P Møller; K Berg
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

6.  Genetic association between eNOS gene polymorphisms and risk of carotid atherosclerosis : A meta-analysis.

Authors:  Yongheng Chen; Lin Chen; Qiliang Zhou
Journal:  Herz       Date:  2020-10-23       Impact factor: 1.443

7.  The effect of the apolipoprotein E phenotype on plasma lipids is not influenced by environmental variability: results of a Dutch twin study.

Authors:  P de Knijff; D I Boomsma; E de Wit; H J Kempen; J A Gevers Leuven; R R Frants; L M Havekes
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

8.  Genetic determination of plasma apolipoprotein AI in a population-based sample.

Authors:  P P Moll; V V Michels; W H Weidman; B A Kottke
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

9.  Variation at the apolipoprotein (apo) AI-CIII-AIV gene cluster and apo B gene loci is associated with lipoprotein and apolipoprotein levels in Italian children.

Authors:  C F Xu; M N Nanjee; J Savill; P J Talmud; F Angelico; M Del Ben; R Antonini; B Mazzarella; N Miller; S E Humphries
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

10.  Sequence polymorphism in kringle IV 37 in linkage disequilibrium with the apolipoprotein (a) size polymorphism.

Authors:  H G Kraft; C Haibach; A Lingenhel; C Brunner; M Trommsdorff; F Kronenberg; H J Müller; G Utermann
Journal:  Hum Genet       Date:  1995-03       Impact factor: 4.132

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