Age-stratified heritability estimation in the Framingham Heart Study families.

Abstract:

:The Framingham Heart Study provides a unique source of longitudinal family data related to CVD risk factors. Age-stratified heritability estimates were obtained over three age groups (31-49 years, 50-60 years, and 61-79 years), reflecting the longitudinal nature of the data, for four quantitative traits. Age-adjusted heritability estimates were obtained at a single common time point for the same four quantitative traits. The importance of these groups is that they consist of the same individuals. The highest age-stratified heritability estimate (h2 = 0.88 (+/- 0.06)) was for height in the model adjusting for gender over all three age groups. SBP gave the lowest heritability estimate (h2 = 0.15 (+/- 0.11)) for the 70 age group in the model adjusting for gender, height, BMI, smoker, and drinker. BMI had slightly higher estimates (h2 = 0.64 (+/- 0.11)) in the 40 age group than previously published. The highest age-adjusted heritability estimate (h2 = 0.90 (+/- 0.06)) was for height in the model adjusting for gender. SBP gave the lowest heritability estimate (h2 = 0.38 (+/- 0.09)) for unadjusted model. These results indicate that some common, complex traits may vary little in their genetic architecture over time and suggest that a common set of genes may be contributing to observed variation for these longitudinally collected phenotypes.

journal_name

BMC Genet

journal_title

BMC genetics

authors

Brown WM,Beck SR,Lange EM,Davis CC,Kay CM,Langefeld CD,Rich SS,Framingham Heart Study.

doi

10.1186/1471-2156-4-S1-S32

keywords:

subject

Has Abstract

pub_date

2003-12-31 00:00:00

pages

S32

issn

1471-2156

pii

1471-2156-4-S1-S32

journal_volume

4 Suppl 1

pub_type

杂志文章
  • Statistically efficient association analysis of quantitative traits with haplotypes and untyped SNPs in family studies.

    abstract:BACKGROUND:Associations between haplotypes and quantitative traits provide valuable information about the genetic basis of complex human diseases. Haplotypes also provide an effective way to deal with untyped SNPs. Two major challenges arise in haplotype-based association analysis of family data. First, haplotypes may ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-020-00902-x

    authors: Diao G,Lin DY

    更新日期:2020-09-07 00:00:00

  • Genome-wide association and systems genetic analyses of residual feed intake, daily feed consumption, backfat and weight gain in pigs.

    abstract:BACKGROUND:Feed efficiency is one of the major components determining costs of animal production. Residual feed intake (RFI) is defined as the difference between the observed and the expected feed intake given a certain production. Residual feed intake 1 (RFI1) was calculated based on regression of individual daily fee...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-15-27

    authors: Do DN,Ostersen T,Strathe AB,Mark T,Jensen J,Kadarmideen HN

    更新日期:2014-02-17 00:00:00

  • Precise single base substitution in the shibire gene by CRISPR/Cas9-mediated homology directed repair in Bactrocera tryoni.

    abstract:BACKGROUND:Pest eradication using the Sterile Insect Technique (SIT) involves high-density releases of sterilized males that mate with wild females and ultimately suppress the population. Sterilized females are not required for SIT and their removal or separation from males prior to release remains challenging. In orde...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-020-00934-3

    authors: Choo A,Fung E,Chen IY,Saint R,Crisp P,Baxter SW

    更新日期:2020-12-18 00:00:00

  • Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome.

    abstract:BACKGROUND:In humans, muscle-specific nicotinergic acetylcholine receptor (AChR) is a transmembrane protein with five different subunits, coded by CHRNA1, CHRNB, CHRND and CHRNG/CHRNE. The gamma subunit of AChR encoded by CHRNG is expressed during early foetal development, whereas in the adult, the γ subunit is replace...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-016-0382-5

    authors: Kariminejad A,Almadani N,Khoshaeen A,Olsson B,Moslemi AR,Tajsharghi H

    更新日期:2016-05-31 00:00:00

  • Fast and accurate haplotype frequency estimation for large haplotype vectors from pooled DNA data.

    abstract:BACKGROUND:Typically, the first phase of a genome wide association study (GWAS) includes genotyping across hundreds of individuals and validation of the most significant SNPs. Allelotyping of pooled genomic DNA is a common approach to reduce the overall cost of the study. Knowledge of haplotype structure can provide ad...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-13-94

    authors: Iliadis A,Anastassiou D,Wang X

    更新日期:2012-10-30 00:00:00

  • Identification and characterization of four Drosophila suzukii cellularization genes and their promoters.

    abstract:BACKGROUND:The spotted-wing Drosophila (Drosophila suzukii) is a widespread invasive pest that causes severe economic damage to fruit crops. The early development of D. suzukii is similar to that of other Drosophilids, but the roles of individual genes must be confirmed experimentally. Cellularization genes coordinate ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-020-00939-y

    authors: Yan Y,Jaffri SA,Schwirz J,Stein C,Schetelig MF

    更新日期:2020-12-18 00:00:00

  • The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis.

    abstract:BACKGROUND:There have been inconsistent results from case-control studies assessing the association of the PON1 Q192R polymorphism with coronary heart disease (CHD). Most studies have included predominantly men and the association in women is unclear. Since lipid levels vary between the sexes the antioxidant effect of ...

    journal_title:BMC genetics

    pub_type: 杂志文章,meta分析,评审

    doi:10.1186/1471-2156-5-17

    authors: Lawlor DA,Day IN,Gaunt TR,Hinks LJ,Briggs PJ,Kiessling M,Timpson N,Smith GD,Ebrahim S

    更新日期:2004-06-23 00:00:00

  • The challenge for genetic epidemiologists: how to analyze large numbers of SNPs in relation to complex diseases.

    abstract::Genetic epidemiologists have taken the challenge to identify genetic polymorphisms involved in the development of diseases. Many have collected data on large numbers of genetic markers but are not familiar with available methods to assess their association with complex diseases. Statistical methods have been developed...

    journal_title:BMC genetics

    pub_type: 社论

    doi:10.1186/1471-2156-7-23

    authors: Heidema AG,Boer JM,Nagelkerke N,Mariman EC,van der A DL,Feskens EJ

    更新日期:2006-04-21 00:00:00

  • The use of the SLC16A1 gene as a potential marker to predict race performance in Arabian horses.

    abstract:BACKGROUND:Arabian horses are commonly believed to be one of the oldest and the most popular horse breeds in the world, characterized by favourable stamina traits and exercise phenotypes. During intensive training, the rates of lactate production and utilization are critical to avoid muscle fatigue and a decrease in ex...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-019-0774-4

    authors: Ropka-Molik K,Stefaniuk-Szmukier M,Szmatoła T,Piórkowska K,Bugno-Poniewierska M

    更新日期:2019-09-11 00:00:00

  • Genetic diversity of Bm86 sequences in Rhipicephalus (Boophilus) microplus ticks from Mexico: analysis of haplotype distribution patterns.

    abstract:BACKGROUND:Ticks are a problem for cattle production mainly in tropical and subtropical regions, because they generate great economic losses. Acaricides and vaccines have been used to try to keep tick populations under control. This has been proven difficult given the resistance to acaricides and vaccines observed in t...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-019-0754-8

    authors: Martínez-Arzate SG,Sánchez-Bermúdez JC,Sotelo-Gómez S,Diaz-Albiter HM,Hegazy-Hassan W,Tenorio-Borroto E,Barbabosa-Pliego A,Vázquez-Chagoyán JC

    更新日期:2019-07-12 00:00:00

  • A power study of bivariate LOD score analysis of a complex trait and fear/discomfort with strangers.

    abstract::Complex diseases are often reported along with disease-related traits (DRT). Sometimes investigators consider both disease and DRT phenotypes separately and sometimes they consider individuals as affected if they have either the disease or the DRT, or both. We propose instead to consider the joint distribution of the ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-S1-S113

    authors: Ji F,Lee D,Mendell NR

    更新日期:2005-12-30 00:00:00

  • A modifier screen in the Drosophila eye reveals that aPKC interacts with Glued during central synapse formation.

    abstract:BACKGROUND:The Glued gene of Drosophila melanogaster encodes the homologue of the vertebrate p150Glued subunit of dynactin. The Glued1 mutation compromises the dynein-dynactin retrograde motor complex and causes disruptions to the adult eye and the CNS, including sensory neurons and the formation of the giant fiber sys...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-10-77

    authors: Ma L,Johns LA,Allen MJ

    更新日期:2009-11-30 00:00:00

  • Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history.

    abstract:BACKGROUND:The N-acetyltransferase 2 (NAT2) gene plays a crucial role in the metabolism of many drugs and xenobiotics. As it represents a likely target of population-specific selection pressures, we fully sequenced the NAT2 coding region in 97 Mandenka individuals from Senegal, and compared these sequences to extant da...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-9-21

    authors: Sabbagh A,Langaney A,Darlu P,Gérard N,Krishnamoorthy R,Poloni ES

    更新日期:2008-02-27 00:00:00

  • Accuracy of genomic prediction for growth and carcass traits in Chinese triple-yellow chickens.

    abstract:BACKGROUND:Growth and carcass traits are very important traits for broiler chickens. However, carcass traits can only be measured postmortem. Genomic selection may be a powerful tool for such traits because of its accurate prediction of breeding values of animals without own phenotypic information. This study investiga...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-014-0110-y

    authors: Liu T,Qu H,Luo C,Shu D,Wang J,Lund MS,Su G

    更新日期:2014-10-15 00:00:00

  • Refining associations between TAS2R38 diplotypes and the 6-n-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children.

    abstract:BACKGROUND:Previous investigations have highlighted the importance of genetic variation in the determination of bitter tasting ability, however have left unaddressed questions as to within group variation in tasting ability or the possibility of genetic prescription of intermediate tasting ability. Our aim was to exami...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-8-51

    authors: Timpson NJ,Heron J,Day IN,Ring SM,Bartoshuk LM,Horwood J,Emmett P,Davey-Smith G

    更新日期:2007-07-28 00:00:00

  • Genomic characterisation, chromosomal assignment and in vivo localisation of the canine high mobility group A1 (HMGA1) gene.

    abstract:BACKGROUND:The high mobility group A1 proteins (HMGA1a/HMGA1b) are highly conserved between mammalian species and widely described as participating in various cellular processes. By inducing DNA conformation changes the HMGA1 proteins indirectly influence the binding of various transcription factors and therefore effec...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-9-49

    authors: Beuing C,Soller JT,Muth M,Wagner S,Dolf G,Schelling C,Richter A,Willenbrock S,Reimann-Berg N,Winkler S,Nolte I,Bullerdiek J,Murua Escobar H

    更新日期:2008-07-23 00:00:00

  • Genetic diversity and population structure of the Sapsaree, a native Korean dog breed.

    abstract:BACKGROUND:The Sapsaree is a breed of dog (Canis familiaris) native to Korea, which became perilously close to extinction in the mid-1980s. However, with systematic genetic conservation and restoration efforts, this breed was rescued from extinction and population sizes have been gradually increasing over the past few ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-019-0757-5

    authors: Gajaweera C,Kang JM,Lee DH,Lee SH,Kim YK,Wijayananda HI,Kim JJ,Ha JH,Choi BH,Lee SH

    更新日期:2019-08-05 00:00:00

  • Correction to: Landraces of snake melon, an ancient Middle Eastern crop, reveal extensive morphological and DNA diversity for potential genetic improvement.

    abstract::Following publication of the original article [1], the authors reported the need for a more detailed acknowledgement of the source of the samples that were analyzed and their coordinates, which are discussed in the 'Methods' section of the article. This Correction provides an addition to the 'Methods' section, and a s...

    journal_title:BMC genetics

    pub_type: 杂志文章,已发布勘误

    doi:10.1186/s12863-018-0632-9

    authors: Omari S,Kamenir Y,Benichou JIC,Pariente S,Sela H,Perl-Treves R

    更新日期:2018-07-12 00:00:00

  • Genome-wide analysis of long non-coding RNAs in Catalpa bungei and their potential function in floral transition using high-throughput sequencing.

    abstract:BACKGROUND:Long non-coding RNAs (lncRNAs) have crucial roles in various biological regulatory processes. However, the study of lncRNAs is limited in woody plants. Catalpa bungei is a valuable ornamental tree with a long cultivation history in China, and a deeper understanding of the floral transition mechanism in C. bu...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-018-0671-2

    authors: Wang Z,Zhu T,Ma W,Wang N,Qu G,Zhang S,Wang J

    更新日期:2018-09-20 00:00:00

  • Computational cloning of drug target genes of a parasitic nematode, Oesophagostomum dentatum.

    abstract:BACKGROUND:Gene identification and sequence determination are critical requirements for many biological, genomic, and bioinformatic studies. With the advent of next generation sequencing (NGS) technologies, such determinations are predominantly accomplished in silico for organisms for which the genome is known or for w...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-14-55

    authors: Romine NM,Martin RJ,Beetham JK

    更新日期:2013-06-18 00:00:00

  • Investigating population continuity with ancient DNA under a spatially explicit simulation framework.

    abstract:BACKGROUND:Recent advances in sequencing technologies have allowed for the retrieval of ancient DNA data (aDNA) from skeletal remains, providing direct genetic snapshots from diverse periods of human prehistory. Comparing samples taken in the same region but at different times, hereafter called "serial samples", may in...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-017-0575-6

    authors: Silva NM,Rio J,Currat M

    更新日期:2017-12-15 00:00:00

  • Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

    abstract:BACKGROUND:DGAT2 is a promising candidate gene for obesity because of its function as a key enzyme in fat metabolism and because of its localization on chromosome 11q13, a linkage region for extreme early onset obesity detected in our sample. We performed a mutation screen in 93 extremely obese children and adolescents...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-8-17

    authors: Friedel S,Reichwald K,Scherag A,Brumm H,Wermter AK,Fries HR,Koberwitz K,Wabitsch M,Meitinger T,Platzer M,Biebermann H,Hinney A,Hebebrand J

    更新日期:2007-05-03 00:00:00

  • ISSR markers show differentiation among Italian populations of Asparagus acutifolius L.

    abstract:BACKGROUND:Asparagus acutifolius L. is a dioecious and native plant species, widely distributed in the Mediterranean Basin. It is known for its fine flavour and could represent an important resource for cultivation programs in desert areas. Few molecular studies have been performed on this species. In the present paper...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-17

    authors: Sica M,Gamba G,Montieri S,Gaudio L,Aceto S

    更新日期:2005-03-18 00:00:00

  • A quantitative linkage score for an association study following a linkage analysis.

    abstract:BACKGROUND:Currently, a commonly used strategy for mapping complex quantitative traits is to use a genome-wide linkage analysis to narrow suspected genes to regions on a scale of centiMorgans (cM), followed by an association analysis to fine map the genetic variation in regions showing linkage. Two important questions ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-7-5

    authors: Wang T,Elston RC

    更新日期:2006-01-20 00:00:00

  • Abnormal X: autosome ratio, but normal X chromosome inactivation in human triploid cultures.

    abstract:BACKGROUND:X chromosome inactivation (XCI) is that aspect of mammalian dosage compensation that brings about equivalence of X-linked gene expression between females and males by inactivating one of the two X chromosomes (Xi) in normal female cells, leaving them with a single active X (Xa) as in male cells. In cells wit...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-7-41

    authors: Gartler SM,Varadarajan KR,Luo P,Norwood TH,Canfield TK,Hansen RS

    更新日期:2006-07-03 00:00:00

  • A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage.

    abstract::A simple multipoint procedure to test for parent-of-origin effects in samples of affected siblings is discussed. The procedure consists of artificially changing all full sibs to half-sibs, with distinct mothers or fathers depending on the parental origin to be evaluated, then analyzing these families with commonly use...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-S1-S159

    authors: Lemire M

    更新日期:2005-12-30 00:00:00

  • Molecular mechanism of estrogen-mediated neuroprotection in the relief of brain ischemic injury.

    abstract:BACKGROUND:This study aimed to explore the molecular mechanism of estrogen-mediated neuroprotection in the relief of cerebral ischemic injury. The gene expression profiles were downloaded from Gene Expression Omnibus database, and differentially expressed genes (DEGs) were identified using limma package in R software. ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-018-0630-y

    authors: He J,Gao Y,Wu G,Lei X,Zhang Y,Pan W,Yu H

    更新日期:2018-07-20 00:00:00

  • Construction of an integrative regulatory element and variation map of the murine Tst locus.

    abstract:BACKGROUND:Given the abundance of new genomic projects and gene annotations, researchers trying to pinpoint causal genetic variants are faced with a challenging task of how to efficiently integrate all current genomic information. The objective of the study was to develop an approach to integrate various genomic annota...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-016-0381-6

    authors: Beltram J,Morton NM,Kunej T,Horvat S

    更新日期:2016-06-11 00:00:00

  • P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility.

    abstract:BACKGROUND:Tumor suppressor gene p53 plays an important role in the maintenance of the genomic integrity, and mutation in the gene may alter an individual's susceptibility to various carcinomas. P53 Arg72Pro or codon 72 polymorphism has been indicated to increase the risk of developing certain cancers such as bladder c...

    journal_title:BMC genetics

    pub_type: 杂志文章,meta分析

    doi:10.1186/s12863-015-0235-7

    authors: Hou J,Gu Y,Hou W,Wu S,Lou Y,Yang W,Zhu L,Hu Y,Sun M,Xue H

    更新日期:2015-06-30 00:00:00

  • In silico genome-wide miRNA-QTL-SNPs analyses identify a functional SNP associated with mastitis in Holsteins.

    abstract:BACKGROUND:Single-nucleotide polymorphisms (SNPs) in microRNAs (miRNAs) and their target binding sites affect miRNA function and are involved in biological processes and diseases, including bovine mastitis, a frequent inflammatory disease. Our previous study has shown that bta-miR-2899 is significantly upregulated in t...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-019-0749-5

    authors: Jiang Q,Zhao H,Li R,Zhang Y,Liu Y,Wang J,Wang X,Ju Z,Liu W,Hou M,Huang J

    更新日期:2019-05-16 00:00:00