Identification of two sex-specific quantitative trait loci in chromosome 11q for hip bone mineral density in Chinese

被引:16
作者
Huang, Qing-Yang
Ng, Mandy Y. M.
Cheung, Ching-Lung
Chan, Vivian
Sham, Pak-Chung
Kung, Annie W. C. [1 ]
机构
[1] Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Genome Res Ctr, Hong Kong, Hong Kong, Peoples R China
关键词
osteoporosis; bone mineral density; genetics; linkage;
D O I
10.1159/000095216
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Chromosome 11q has not only been found to contain mutations responsible for the several Mendelian disorders of the skeleton, but it has also been linked to bone mineral density (BMD) variation in several genome-wide linkage studies. Furthermore, quantitative trait loci (QTL) affecting BMD in inbred mice and baboons have been mapped to a region syntenic to human chromosome 11q. The aim of the present study is to determine whether there is a QTL for BMD variation on chromosome 11q in the Chinese population. Methods: Nineteen microsatellite markers were genotyped for a 75 cM region on 11q13-25 in 306 Chinese families with 1,459 subjects. BMD (g/cm(2)) was measured by DXA. Linkage analyses were performed using the variance component linkage analysis method implemented in Merlin software. Results: For women, a maximum LOD score of 1.62 was achieved at 90.8 cM on 11q21 near the marker D11S4175 for femoral neck BMD; LOD scores greater than 1.0 were observed on 11q13 for trochanter BMD. For men, a maximum LOD score of 1.57 was achieved at 135.8 cM on 11q24 near the marker D11S4126 for total hip BMD. Conclusion: We have not only replicated the previous linkage finding on chromosome 11q but also identified two sex-specific QTL that contribute to BMD variation in Chinese women and men. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:237 / 243
页数:7
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