Maturitas
Volume 55, Issue 4 , Pages 325-333, 20 November 2006

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

  • Fréderique Retornaz

      Affiliations

    • Department of Internal Medicine and Geriatrics, University Hospital, Montpellier, France
    • Department of Hormonology, University Hospital, Montpellier, France
  • ,
  • Françoise Paris

      Affiliations

    • Department of Hormonology, University Hospital, Montpellier, France
  • ,
  • Serge Lumbroso

      Affiliations

    • Department of Hormonology, University Hospital, Montpellier, France
  • ,
  • Françoise Audran

      Affiliations

    • Department of Hormonology, University Hospital, Montpellier, France
  • ,
  • Fabien Tigoulet

      Affiliations

    • Department of Internal Medicine and Geriatrics, University Hospital, Montpellier, France
  • ,
  • Cécile Michelon

      Affiliations

    • Department of Medical Information, University Hospital, Montpellier, France
  • ,
  • Claude Jeandel

      Affiliations

    • Department of Internal Medicine and Geriatrics, University Hospital, Montpellier, France
  • ,
  • Charles Sultan

      Affiliations

    • Department of Hormonology, University Hospital, Montpellier, France
  • ,
  • Hubert Blain

      Affiliations

    • Department of Internal Medicine and Geriatrics, University Hospital, Montpellier, France
    • Corresponding Author InformationCorresponding author. Tel.: +33 467336778; fax: +33 467336887.

Received 21 November 2005; received in revised form 25 April 2006; accepted 28 April 2006.

Abstract 

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.

Keywords: Androgen receptor polymorphism, X-chromosome inactivation, Bone mineral density, Postmenopausal women, Osteoporosis, CAG repeat

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PII: S0378-5122(06)00162-9

doi:10.1016/j.maturitas.2006.04.025

Maturitas
Volume 55, Issue 4 , Pages 325-333, 20 November 2006