Related Experiment Video
Updated: Dec 30, 2025

06:18
An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
12.7K
Transdermal Estrogen in Women With Anorexia Nervosa: An Exploratory Pilot Study
Megi Resulaj1, Sai Polineni1, Erinne Meenaghan1
1Neuroendocrine Unit Massachusetts General Hospital Boston MA USA.
JBMR Plus
|January 21, 2020
Summary
Transdermal estrogen therapy improved bone mineral density (BMD) in women with anorexia nervosa (AN). This treatment also reduced bone marrow adipose tissue (BMAT), a key factor in AN-related bone loss.
Area of Science:
- Bone and Mineral Research
- Endocrinology
- Psychiatric Disorders
Background:
- Anorexia nervosa (AN) is associated with low bone mineral density (BMD) and increased fracture risk, partly due to elevated bone marrow adipose tissue (BMAT).
- Standard oral estrogen therapies are ineffective for increasing bone mass in women with AN, despite amenorrhea being common.
Purpose of the Study:
- To investigate the effects of transdermal estradiol plus levonorgestrel on BMD and BMAT in women with AN.
- To assess changes in bone turnover markers and other relevant biomarkers.
Main Methods:
- A 6-month, open-label study involving 11 women with AN.
- Transdermal estradiol (0.045 mg/day) plus levonorgestrel (0.015 mg/day) was administered.
- BMD was measured by DXA, BMAT by 1H-magnetic resonance spectroscopy, and bone turnover markers were analyzed at 3 and 6 months.
Main Results:
- Lumbar spine BMD increased by 2.0% and lateral spine BMD by 3.2% after 6 months (p < 0.05).
- Lumbar spine BMAT significantly decreased by 13.9% after 3 months (p = 0.046).
- Increases in lateral spine BMD correlated with decreases in C-terminal collagen cross-links (CTX) (p = 0.047).
Conclusions:
- Short-term treatment with transdermal physiologic estrogen effectively increases spine BMD in women with anorexia nervosa.
- Transdermal estrogen therapy may help mitigate bone loss in AN by reducing BMAT and bone resorption.

