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Withdrawal of hormone replacement therapy is associated with significant vertebral bone loss in postmenopausal women
F A Trémollieres1, J M Pouilles, C Ribot
1Menopause and Bone Metabolic Diseases Unit, Endocrinology Department, CHU Rangueil, 1, avenue Jean Poulhès, F-31403 Toulouse, France. tremollieres.f@chu-toulouse.fr
Insights
Bone mineral density (BMD) loss accelerates after stopping hormone replacement therapy (HRT), mirroring natural menopause rates. However, long-term vertebral BMD remains higher than pre-treatment levels, suggesting a lasting benefit.
Area of Science:
- Endocrinology
- Bone Metabolism
- Gerontology
Background:
- Postmenopausal osteoporosis is a significant health concern.
- Hormone replacement therapy (HRT) is used to manage menopausal symptoms and prevent bone loss.
- The long-term effects of HRT cessation on bone mineral density (BMD) require further investigation.
Purpose of the Study:
- To assess changes in vertebral bone mineral density (BMD) after long-term hormone replacement therapy (HRT) cessation in postmenopausal women.
- To compare bone loss patterns after HRT withdrawal with those in untreated postmenopausal women.
- To evaluate any residual effects of prior HRT on bone mass.
Main Methods:
- Longitudinal study of 50 healthy postmenopausal women with prior long-term HRT.
- Vertebral BMD measurements during HRT and at intervals after cessation (up to 8 years).
- Comparison with a control group of untreated postmenopausal women.
Main Results:
- Bone loss accelerated within the first 2 years after HRT cessation, comparable to untreated women.
- After 2 years, the rate of bone loss decreased, similar to natural menopause.
- Mean vertebral BMD 3 years post-cessation was significantly higher than baseline (pre-HRT).
Conclusions:
- Bone loss after estrogen therapy cessation resembles that of early postmenopause in untreated women.
- This pattern should be considered when discontinuing HRT, particularly for osteoporosis prevention.
- Further research is needed to determine long-term residual benefits on bone mass and fracture risk.
Abstract:
This study aimed to assess the changes in vertebral bone mineral density (BMD) after cessation of hormone replacement therapy (HRT) in postmenopausal women who had been treated on a long-term basis. Fifty healthy postmenopausal women who had been followed both during the course of HRT and after cessation of treatment in our menopause clinic were included in this study. All women had started HRT within the first 3 years after the postmenopause and had received HRT (either 1.5 mg/day of 17 beta-estradiol given percutaneously or 50 micrograms/day of 17 beta-estradiol given as a transdermal patch, combined in all women with natural progesterone or a 19-norprogesterone derivative) for a mean 5 +/- 2.4 years. In all women, vertebral BMD was assessed during the course of HRT up to the last 6 months before estrogen withdrawal, then at least once within the first 18 months after cessation of treatment. Of the initial population, 30 women were additionally reviewed later on and up to 8 years after cessation of treatment (mean duration of follow-up for the whole population: 3.9 +/- 1.7 years). Rates of changes in vertebral BMD were compared with those determined in a group of healthy untreated women who had been followed within the first years of postmenopause during the same time period as the study population. In the study group, bone loss was found to accelerate within the first 2 years after HRT withdrawal and the annual rate of loss was identical to that which occurs within the first 2 years of postmenopause in untreated women (-1.64% +/- 1.3% vs -1.52 +/- 0.9%, NS). Beyond this first 2-year time period, the annual rate of bone loss decreased as a function of time following cessation of treatment, as was observed following the menopause in untreated women (between 3 and 5 years: -0.83% + 1.35% in the study group vs -0.70% +/- 0.8% in the control group, NS). On average, 3 years after cessation of HRT mean vertebral BMD when expressed as a Z-score was significantly higher (-0.13 vs -0.89, p < 0.01) than at baseline, before HRT was started, which suggested a lasting beneficial effect on bone mass. However, even though our findings do not support the hypothesis that bone loss might continue to be accelerated several years after cessation of treatment we cannot fully address the question as to whether any residual benefit on bone mass over a longer period of time may be observed. In conclusion, the pattern of bone loss observed after cessation of estrogen therapy was found to be comparable to that which occurs in younger women within the first years after the menopause. Such a pattern needs to be kept in mind when the decision to stop HRT is taken, especially in women who were given HRT to prevent osteoporosis. The issue of assessing their risk of fracture several years after cessation of treatment thus needs to be addressed.
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