Abstract

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.

Highlights

  • IntroductionHeritability estimates measured in previous studies range from 0.68–0.98 (with men having higher heritability than women) [1;2]

  • Human height is a highly heritable and complex trait

  • MZ twins had significantly higher intra-class correlations (ICC) than DZ twins and the highest heritability was found for length of femur at 73%

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Summary

Introduction

Heritability estimates measured in previous studies range from 0.68–0.98 (with men having higher heritability than women) [1;2]. The polygenic and heterogeneic nature of height means that it may be difficult to find causal genes and explains the lack of success to date in previous studies despite large numbers [3,4,5,6]. Previous studies have shown demi-span and lower limb length as useful surrogates for height [7,8,9,10]. Sub-compartments of bone and skeletal measures are highly heritable [10,11,12,13], for example, hip axis length with a heritability of 62% [11]

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