Association between androgen receptor gene polymorphism and bone density in older women using hormone replacement therapy

被引:11
作者
Retornaz, Frederique
Paris, Francoise
Lumbroso, Serge
Audran, Francoise
Tigoulet, Fabien
Michelon, Cecile
Jeandel, Claude
Sultan, Charles
Blain, Hubert [1 ]
机构
[1] Univ Hosp Montpellier, Dept Internal Med & Geriatr, Montpellier, France
[2] Univ Hosp Montpellier, Dept Hormonol, Montpellier, France
[3] Univ Hosp Montpellier, Dept Med Informat, Montpellier, France
关键词
androgen receptor polymorphism; X-chromosome inactivation; bone mineral density; postmenopausal women; osteoporosis; CAG repeat;
D O I
10.1016/j.maturitas.2006.04.025
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
Objective: The objective of this study was to investigate the relationship between bone mineral density (BMD) and both CAG repeat polymorphism of the androgen receptor (AR) gene and skewed X chromosome inactivation (SI) in postmenopausal women. Methods: BMD was measured by DEXA. Both the number and the X-weighted biallelic mean of the CAG repeats of AR were analysed by PCR, before and after DNA digestion with methylation-sensitive HpaII in 192 healthy Caucasian postmenopausal women. Results: The number of CAG repeats ranged from 10 to 34, with a median value of 22. CAG)(n <= 22) and CAG)(n >= 23) alleles were designated as short and long alleles, respectively. In women using hormone replacement therapy (HRT) (n=81), lumbar spine BMD was significantly lower, and femoral neck and total body BMD marginally lower in those with long-long alleles when compared with those with other genotypes. SI (>= 80%) was observed in 24% of the women and was not associated with BMD. In women using HRT, femoral neck BMD was significantly lower, and lumbar spine and total body BMD marginally lower in those whose X-weighted CAG repeat biallelic was greater than 22.59 (median value) when compared to other genotypes. These results were not found in women not using HRT. Conclusion: In conclusion, our results suggest that BMD may be associated with AR gene polymorphism in postmenopausal women using HRT but not with SI. Further studies are needed to investigate the mechanisms of the interaction between HRT, BMD and AR found in the present study. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:325 / 333
页数:9
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