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Age-stratified heritability estimation in the Framingham Heart Study families
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 tr...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866468/ https://www.ncbi.nlm.nih.gov/pubmed/14975100 http://dx.doi.org/10.1186/1471-2156-4-S1-S32 |
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author | Brown, W Mark Beck, Stephanie R Lange, Ethan M Davis, Cralen C Kay, Christine M Langefeld, Carl D Rich, Stephen S |
author_facet | Brown, W Mark Beck, Stephanie R Lange, Ethan M Davis, Cralen C Kay, Christine M Langefeld, Carl D Rich, Stephen S |
author_sort | Brown, W Mark |
collection | PubMed |
description | 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 (h(2 )= 0.88 (± 0.06)) was for height in the model adjusting for gender over all three age groups. SBP gave the lowest heritability estimate (h(2 )= 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 (h(2 )= 0.64 (± 0.11)) in the 40 age group than previously published. The highest age-adjusted heritability estimate (h(2 )= 0.90 (± 0.06)) was for height in the model adjusting for gender. SBP gave the lowest heritability estimate (h(2 )= 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. |
format | Text |
id | pubmed-1866468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18664682007-05-11 Age-stratified heritability estimation in the Framingham Heart Study families Brown, W Mark Beck, Stephanie R Lange, Ethan M Davis, Cralen C Kay, Christine M Langefeld, Carl D Rich, Stephen S BMC Genet Proceedings 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 (h(2 )= 0.88 (± 0.06)) was for height in the model adjusting for gender over all three age groups. SBP gave the lowest heritability estimate (h(2 )= 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 (h(2 )= 0.64 (± 0.11)) in the 40 age group than previously published. The highest age-adjusted heritability estimate (h(2 )= 0.90 (± 0.06)) was for height in the model adjusting for gender. SBP gave the lowest heritability estimate (h(2 )= 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. BioMed Central 2003-12-31 /pmc/articles/PMC1866468/ /pubmed/14975100 http://dx.doi.org/10.1186/1471-2156-4-S1-S32 Text en Copyright © 2003 Brown et al; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Brown, W Mark Beck, Stephanie R Lange, Ethan M Davis, Cralen C Kay, Christine M Langefeld, Carl D Rich, Stephen S Age-stratified heritability estimation in the Framingham Heart Study families |
title | Age-stratified heritability estimation in the Framingham Heart Study families |
title_full | Age-stratified heritability estimation in the Framingham Heart Study families |
title_fullStr | Age-stratified heritability estimation in the Framingham Heart Study families |
title_full_unstemmed | Age-stratified heritability estimation in the Framingham Heart Study families |
title_short | Age-stratified heritability estimation in the Framingham Heart Study families |
title_sort | age-stratified heritability estimation in the framingham heart study families |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866468/ https://www.ncbi.nlm.nih.gov/pubmed/14975100 http://dx.doi.org/10.1186/1471-2156-4-S1-S32 |
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