Effect of ultra-low-dose estradiol and dydrogesterone on arterial stiffness in postmenopausal women

Abstract Background Ultra-low-dose estradiol is known to improve menopausal symptoms and increase bone mineral density. However, the effect of ultra-low-dose estradiol on vascular function has not been clarified. Objectives We examined the effects of ultra-low-dose estradiol on brachial-ankle pulse...

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Published in:Climacteric : the journal of the International Menopause Society Vol. 17; no. 2; pp. 191 - 196
Main Authors: Matsui, S., Yasui, T., Tani, A., Kato, T., Uemura, H., Kuwahara, A., Matsuzaki, T., Arisawa, K., Irahara, M.
Format: Journal Article
Language:English
Published: England Informa Healthcare 01-04-2014
Taylor & Francis
Taylor & Francis Ltd
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Summary:Abstract Background Ultra-low-dose estradiol is known to improve menopausal symptoms and increase bone mineral density. However, the effect of ultra-low-dose estradiol on vascular function has not been clarified. Objectives We examined the effects of ultra-low-dose estradiol on brachial-ankle pulse wave velocity (baPWV) and circulating markers of cardiovascular risk. Patients and methods Twenty-eight postmenopausal women were enrolled in this study. Fourteen women received oral estradiol (0.5 mg) and dydrogesterone (5 mg) every day for 12 months (ultra-low-dose group) as hormone replacement therapy (HRT) and 14 women as a control group did not receive HRT. The baPWV, lipid profiles, homeostasis model assessment of insulin resistance (HOMA-IR) and vascular inflammatory markers were measured. Results The baPWV level significantly decreased in the ultra-low-dose group (p = 0.037), while the baPWV level did not significantly change in the control group. HOMA-IR tended to decrease in the ultra-low-dose group (p = 0.076). Systolic blood pressure and diastolic blood pressure did not change significantly in either group. Conclusion An HRT regimen using oral ultra-low-dose estradiol and dydrogesterone has an effect on arterial stiffness and insulin resistance.
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ISSN:1369-7137
1473-0804
DOI:10.3109/13697137.2013.856399