Cargando…

Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort

Human height is a highly heritable and complex trait but finding important genes has proven more difficult than expected. One reason might be the composite measure of height which may add heterogeneity and noise. The aim of this study was to conduct a genome-wide linkage scan to identify quantitativ...

Descripción completa

Detalles Bibliográficos
Autores principales: Chinappen-Horsley, Usha, Blake, Glen M., Fogelman, Ignac, Kato, Bernet, Ahmadi, Kourosh R., Spector, Tim D.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2262137/
https://www.ncbi.nlm.nih.gov/pubmed/18335030
http://dx.doi.org/10.1371/journal.pone.0001752
_version_ 1782151409132634112
author Chinappen-Horsley, Usha
Blake, Glen M.
Fogelman, Ignac
Kato, Bernet
Ahmadi, Kourosh R.
Spector, Tim D.
author_facet Chinappen-Horsley, Usha
Blake, Glen M.
Fogelman, Ignac
Kato, Bernet
Ahmadi, Kourosh R.
Spector, Tim D.
author_sort Chinappen-Horsley, Usha
collection PubMed
description Human height is a highly heritable and complex trait but finding important genes has proven more difficult than expected. One reason might be the composite measure of height which may add heterogeneity and noise. The aim of this study was to conduct a genome-wide linkage scan to identify quantitative trait loci (QTL) for lengths of spine, femur, tibia, humerus and radius. These were investigated as alternative measures for height in a large, population–based twin sample with the potential to find genes underlying bone size and bone diseases. 3,782 normal Caucasian females, 18–80 years old, with whole body dual energy X-ray absorptiometry (DXA) images were used. A novel and reproducible method, linear pixel count (LPC) was used to measure skeletal sizes on DXA images. Intraclass correlations and heritability estimates were calculated for lengths of spine, femur, tibia, humerus and radius on monozygotic (MZ; n = 1,157) and dizygotic (DZ; n = 2,594) twins. A genome-wide linkage scan was performed on 2000 DZ twin subjects. All skeletal sites excluding spine were highly correlated. Intraclass correlations showed results for MZ twins to be significantly higher than DZ twins for all traits. Heritability results were as follows: spine, 66%; femur, 73%; tibia, 65%; humerus, 57%; radius, 68%. Results showed reliable evidence of highly suggestive linkage on chromosome 5 for spine (LOD score  =  3.0) and suggestive linkage for femur (LOD score  =  2.19) in the regions of 105cM and 155cM respectively. We have shown strong heritability of all skeletal sizes measured in this study and provide preliminary evidence that spine length is linked to the chromosomal region 5q15-5q23.1. Bone size phenotype appears to be more useful than traditional height measures to uncover novel genes. Replication and further fine mapping of this region is ongoing to determine potential genes influencing bone size and diseases affecting bone.
format Text
id pubmed-2262137
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-22621372008-03-12 Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort Chinappen-Horsley, Usha Blake, Glen M. Fogelman, Ignac Kato, Bernet Ahmadi, Kourosh R. Spector, Tim D. PLoS One Research Article Human height is a highly heritable and complex trait but finding important genes has proven more difficult than expected. One reason might be the composite measure of height which may add heterogeneity and noise. The aim of this study was to conduct a genome-wide linkage scan to identify quantitative trait loci (QTL) for lengths of spine, femur, tibia, humerus and radius. These were investigated as alternative measures for height in a large, population–based twin sample with the potential to find genes underlying bone size and bone diseases. 3,782 normal Caucasian females, 18–80 years old, with whole body dual energy X-ray absorptiometry (DXA) images were used. A novel and reproducible method, linear pixel count (LPC) was used to measure skeletal sizes on DXA images. Intraclass correlations and heritability estimates were calculated for lengths of spine, femur, tibia, humerus and radius on monozygotic (MZ; n = 1,157) and dizygotic (DZ; n = 2,594) twins. A genome-wide linkage scan was performed on 2000 DZ twin subjects. All skeletal sites excluding spine were highly correlated. Intraclass correlations showed results for MZ twins to be significantly higher than DZ twins for all traits. Heritability results were as follows: spine, 66%; femur, 73%; tibia, 65%; humerus, 57%; radius, 68%. Results showed reliable evidence of highly suggestive linkage on chromosome 5 for spine (LOD score  =  3.0) and suggestive linkage for femur (LOD score  =  2.19) in the regions of 105cM and 155cM respectively. We have shown strong heritability of all skeletal sizes measured in this study and provide preliminary evidence that spine length is linked to the chromosomal region 5q15-5q23.1. Bone size phenotype appears to be more useful than traditional height measures to uncover novel genes. Replication and further fine mapping of this region is ongoing to determine potential genes influencing bone size and diseases affecting bone. Public Library of Science 2008-03-12 /pmc/articles/PMC2262137/ /pubmed/18335030 http://dx.doi.org/10.1371/journal.pone.0001752 Text en Chinappen-Horsley et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chinappen-Horsley, Usha
Blake, Glen M.
Fogelman, Ignac
Kato, Bernet
Ahmadi, Kourosh R.
Spector, Tim D.
Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort
title Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort
title_full Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort
title_fullStr Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort
title_full_unstemmed Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort
title_short Quantitative Trait Loci for Bone Lengths on Chromosome 5 Using Dual Energy X-Ray Absorptiometry Imaging in the Twins UK Cohort
title_sort quantitative trait loci for bone lengths on chromosome 5 using dual energy x-ray absorptiometry imaging in the twins uk cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2262137/
https://www.ncbi.nlm.nih.gov/pubmed/18335030
http://dx.doi.org/10.1371/journal.pone.0001752
work_keys_str_mv AT chinappenhorsleyusha quantitativetraitlociforbonelengthsonchromosome5usingdualenergyxrayabsorptiometryimaginginthetwinsukcohort
AT blakeglenm quantitativetraitlociforbonelengthsonchromosome5usingdualenergyxrayabsorptiometryimaginginthetwinsukcohort
AT fogelmanignac quantitativetraitlociforbonelengthsonchromosome5usingdualenergyxrayabsorptiometryimaginginthetwinsukcohort
AT katobernet quantitativetraitlociforbonelengthsonchromosome5usingdualenergyxrayabsorptiometryimaginginthetwinsukcohort
AT ahmadikouroshr quantitativetraitlociforbonelengthsonchromosome5usingdualenergyxrayabsorptiometryimaginginthetwinsukcohort
AT spectortimd quantitativetraitlociforbonelengthsonchromosome5usingdualenergyxrayabsorptiometryimaginginthetwinsukcohort