Twice-weekly transdermal estradiol and vaginal progesterone as continuous combined hormone replacement therapy in postmenopausal women: A 1-year prospective study

2002 ◽  
Vol 187 (3) ◽  
pp. 556-560 ◽  
Author(s):  
Ettore Cicinelli ◽  
Dominique de Ziegler ◽  
Pietro Galantino ◽  
Vincenzo Pinto ◽  
Bruno Barba ◽  
...  
2006 ◽  
Vol 91 (8) ◽  
pp. 3123-3130 ◽  
Author(s):  
K. C. Lewandowski ◽  
J. Komorowski ◽  
D. P. Mikhalidis ◽  
M. Bienkiewicz ◽  
B. K. Tan ◽  
...  

Abstract Background: Matrix metalloproteinases (MMPs) are implicated in numerous disease states including cardiovascular disease and cancer. Because recent studies have shown a detrimental effect of hormone replacement therapy on cardiovascular disease and breast cancer, we investigated whether there are any differences in the concentrations of MMPs and their tissue inhibitors (TIMPs) in women receiving various forms of postmenopausal therapy. Material and Methods: A total of 195 healthy postmenopausal women were assessed: 46 were taking tibolone, 47 were taking transdermal estradiol, 46 were taking conjugated equine estrogens (CEE), and 56 were not taking any menopausal therapy (CTR). Plasma levels of MMP-2 and -9 and TIMP-1 and TIMP-2 were measured by ELISA methods. Results: MMP-9 levels were significantly higher in the CEE group in comparison with healthy women not receiving menopausal therapy (P < 0.05). In contrast, MMP-9 levels in the tibolone group were significantly lower than in any other group (P < 0.01, compared with transdermal estradiol and CTR, and P < 0.001, compared with CEE). MMP-9 to TIMP-1 ratio was also significantly higher in the CEE, compared with CTR (P < 0.05), and lower in the tibolone group (P < 0.01, compared with all groups). MMP-2 levels were higher in the CEE group, compared with healthy women not receiving any menopausal therapy, and women taking tibolone (P < 0.05). Conclusions: Our study demonstrates differential effects of various forms of postmenopausal therapy on serum levels of MMP-9 and MMP-2. It remains to be established whether these differences might be associated with differences in risks of cardiovascular disease and cancer in these women.


2003 ◽  
Vol 79 (2) ◽  
pp. 274-280 ◽  
Author(s):  
Byung-Koo Yoon ◽  
Doh Kwan Kim ◽  
Yeonwook Kang ◽  
Jong-Won Kim ◽  
Myung-Hee Shin ◽  
...  

Maturitas ◽  
1999 ◽  
Vol 31 (2) ◽  
pp. 143-149 ◽  
Author(s):  
A.L.M Kok ◽  
C.W Burger ◽  
P.H.M van de Weijer ◽  
G.A Voetberg ◽  
E.R.A Peters-Muller ◽  
...  

1999 ◽  
Vol 81 (05) ◽  
pp. 673-675 ◽  
Author(s):  
Martine Alhenc-Gelas ◽  
Emmanuel Oger ◽  
Geneviève Plu-Bureau ◽  
Pierre-Yves Scarabin

SummaryHormone replacement therapy may reduce the risk of coronary heart disease but underlying mechanism has not been adequately explained. Recent data suggest that intercellular adhesion molecule 1 (ICAM-1) plays a critical role in early stage of atherosclerosis and may serve as a molecular marker for the development of arterial disease. We investigated the effects of oral and transdermal cyclic oestradiol combined with progesterone on plasma concentration of soluble ICAM-1 (sICAM-1). Thirty-seven healthy postmenopausal women were randomly assigned to receive either oral estradiol valerate or transdermal estradiol both combined with micronized progesterone or no hormonal treatment. Plasma sICAM-1 was assayed at baseline and after a 6-month period. Oral but not transdermal estradiol regimen significantly decreased mean value of sICAM-1 compared with no treatment. Differences in sICAM-1 levels between active treatments were significant. There were no significant changes in mean values of fibrinogen between the three groups. Our results show a favorable effect of oral estrogen plus progesterone on a soluble marker of vascular inflammation and may provide plausible explanation for a cardioprotective effect of hormone replacement therapy among healthy postmenopausal women.


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