Literature DB >> 11052548

Familial patterns of covariation for cardiovascular risk factors in adults: The Victorian Family Heart Study.

S B Harrap1, M Stebbing, J L Hopper, H N Hoang, G G Giles.   

Abstract

The Victorian Family Heart Study was established to address the causes of familial patterns in cardiovascular risk factors. From 1990 to 1996, a representative population sample of 783 adult families (2,959 individuals), each comprising both parents (40-70 years) and at least one natural adult offspring (18-30 years), was recruited in Melbourne, Australia. Included in both generations were 461 monozygotic and dizygotic twins as pairs or singletons. A multivariate normal model was used for pedigree analysis of height, weight, body mass index, diastolic and systolic blood pressure, pulse rate, and total and high density lipoprotein cholesterol. All traits showed evidence for additive genetic variation, explaining from 55% (height) to 26% (pulse) of age- and sex-adjusted variance. An effect persisting into adulthood of shared family environment during cohabitation explained from 39% (body mass index) to 13% (systolic blood pressure) of variance (not nominally significant for diastolic blood pressure). These shared environmental effects were strongest within twin pairs, less so for sibling pairs, and least for parent-offspring pairs (in which an effect was not observed for weight, diastolic and systolic blood pressure, and total cholesterol). On a background of genetic influences, there are periods in early life during which the family environment cements long-term correlations between adult relatives in cardiovascular risk factors.

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Year:  2000        PMID: 11052548     DOI: 10.1093/aje/152.8.704

Source DB:  PubMed          Journal:  Am J Epidemiol        ISSN: 0002-9262            Impact factor:   4.897


  35 in total

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Journal:  Hum Genet       Date:  2006-03-29       Impact factor: 4.132

4.  Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population.

Authors:  Justine A Ellis; Katrina J Scurrah; Anna E Duncan; Angela Lamantia; Graham B Byrnes; Stephen B Harrap
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Authors:  Justine A Ellis; Katrina J Scurrah; Joanna E Cobb; Sophie G Zaloumis; Anna E Duncan; Stephen B Harrap
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6.  Genetic architecture of lipid traits changes over time and differs by race: Princeton Lipid Follow-up Study.

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8.  Impact of interactions between risk alleles on clinical endpoints in hypertension.

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Journal:  Heart Asia       Date:  2016-05-19

9.  A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

Authors:  Elizabeth R Hauser; David C Crossman; Christopher B Granger; Jonathan L Haines; Christopher J H Jones; Vincent Mooser; Brendan McAdam; Bernhard R Winkelmann; Alan H Wiseman; J Brent Muhlestein; Alan G Bartel; Charles A Dennis; Elaine Dowdy; Susan Estabrooks; Karen Eggleston; Sheila Francis; Kath Roche; Paula W Clevenger; Liling Huang; Bonnie Pedersen; Svati Shah; Silke Schmidt; Carol Haynes; Sandra West; Donny Asper; Michael Booze; Sanjay Sharma; Scott Sundseth; Lefkos Middleton; Allen D Roses; Michael A Hauser; Jeffery M Vance; Margaret A Pericak-Vance; William E Kraus
Journal:  Am J Hum Genet       Date:  2004-07-22       Impact factor: 11.025

10.  Intergenerational cardiovascular disease risk factors involve both maternal and paternal BMI.

Authors:  Idoia Labayen; Jonatan R Ruiz; Francisco B Ortega; Helle-Mai Loit; Jaanus Harro; Toomas Veidebaum; Michael Sjöström
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