Effects of conventional or lower doses of hormone replacement therapy in postmenopausal women
- PMID: 15166013
- DOI: 10.1161/01.ATV.0000133683.65877.bc
Effects of conventional or lower doses of hormone replacement therapy in postmenopausal women
Abstract
Objective: The effects of hormone replacement therapy (HRT) can affect many aspects relevant to cardiovascular disease, including vasomotor function, inflammation, and hemostasis. Recent studies have demonstrated that current doses of HRT exert a mixture of both protective and adverse effects. In the current study, we compared the effects of lower doses of HRT (L-HRT) and conventional doses of HRT (C-HRT) on a variety of relevant cardiovascular parameters.
Methods and results: This randomized, double-blind, crossover study included 57 women who received micronized progesterone 100 mg with either conjugated equine estrogen 0.625 mg (C-HRT) or 0.3 mg (L-HRT) daily for 2 months. L-HRT showed comparable effects to C-HRT on high-density lipoprotein cholesterol and triglyceride levels, but not on low-density lipoprotein cholesterol levels. C-HRT and L-HRT significantly improved the percent flow-mediated dilator response to hyperemia from baseline values (both P<0.001) by a similar degree (P=0.719). C-HRT significantly increased high-sensitivity C-reactive protein (hsCRP) levels from baseline values (P<0.001); however, L-HRT did not significantly change hsCRP (P=0.874). C-HRT and L-HRT significantly decreased antithrombin III from baseline values (P<0.001 and P=0.042, respectively). C-HRT significantly increased prothrombin fragment 1+2 (F1+2) from baseline values (P<0.001); however, L-HRT did not significantly change F1+2 (P=0.558). Of interest, the effects of C-HRT and L-HRT on hsCRP, antithrombin III, and F1+2 were significantly different (all P<0.001). C-HRT and L-HRT significantly reduced plasma PAI-1 antigen levels from baseline values (P=0.002 and P=0.038, respectively) to a similar degree (P=0.184).
Conclusions: Compared with C-HRT, L-HRT has comparable effects on lipoproteins, flow-mediated dilation, and PAI-1 antigen levels. However, L-HRT did not increase hsCRP or F1+2 levels, and it decreased antithrombin III less than C-HRT.
Comment in
-
Lower doses of estrogen replacement therapy and the risk of cardiovascular disease.Arterioscler Thromb Vasc Biol. 2004 Dec;24(12):e197; author reply e197. doi: 10.1161/01.ATV.0000148203.03346.b5. Arterioscler Thromb Vasc Biol. 2004. PMID: 15576640 Review. No abstract available.
Similar articles
-
Significant differential effects of lower doses of hormone therapy or tibolone on markers of cardiovascular disease in post-menopausal women: a randomized, double-blind, crossover study.Eur Heart J. 2005 Jul;26(14):1362-8. doi: 10.1093/eurheartj/ehi311. Epub 2005 May 4. Eur Heart J. 2005. PMID: 15872028 Clinical Trial.
-
Significant differential effects of hormone therapy or tibolone on markers of cardiovascular disease in postmenopausal women: a randomized, double-blind, placebo-controlled, crossover study.Arterioscler Thromb Vasc Biol. 2003 Oct 1;23(10):1889-94. doi: 10.1161/01.ATV.0000091502.96745.95. Epub 2003 Aug 21. Arterioscler Thromb Vasc Biol. 2003. PMID: 12933531 Clinical Trial.
-
Lipid profiles and endothelial function with low-dose hormone replacement therapy in postmenopausal women at risk for coronary artery disease: a randomized trial.Int J Cardiol. 2003 Jun;89(2-3):257-65. doi: 10.1016/s0167-5273(02)00505-3. Int J Cardiol. 2003. PMID: 12767550 Clinical Trial.
-
Effects of hormone replacement therapy on coagulation and fibrinolysis in postmenopausal women.Int J Hematol. 2002 Aug;76 Suppl 2:44-6. doi: 10.1007/BF03165085. Int J Hematol. 2002. PMID: 12430899 Review.
-
Should progestins be blamed for the failure of hormone replacement therapy to reduce cardiovascular events in randomized controlled trials?Arterioscler Thromb Vasc Biol. 2004 Jul;24(7):1171-9. doi: 10.1161/01.ATV.0000131262.98040.65. Epub 2004 May 6. Arterioscler Thromb Vasc Biol. 2004. PMID: 15130916 Review.
Cited by
-
Vasomotor Symptoms During Menopause: A Practical Guide on Current Treatments and Future Perspectives.Int J Womens Health. 2023 Feb 14;15:273-287. doi: 10.2147/IJWH.S365808. eCollection 2023. Int J Womens Health. 2023. PMID: 36820056 Free PMC article. Review.
-
Research into Specific Modulators of Vascular Sex Hormone Receptors in the Management of Postmenopausal Cardiovascular Disease.Curr Hypertens Rev. 2009 Nov;5(4):283-306. doi: 10.2174/157340209789587717. Curr Hypertens Rev. 2009. PMID: 20694192 Free PMC article.
-
Variation of endothelial function during the menstrual cycle evaluated by flow-mediated dilatation of brachial artery.JBRA Assist Reprod. 2014 Dec 27;18(4):148-150. doi: 10.5935/1518-0557.20140022. JBRA Assist Reprod. 2014. PMID: 35761744 Free PMC article.
-
Effect of hormone therapy and calcitriol on serum lipid profile in postmenopausal older women: association with estrogen receptor-α genotypes.Menopause. 2011 Oct;18(10):1101-12. doi: 10.1097/gme.0b013e318217d41d. Menopause. 2011. PMID: 21712736 Free PMC article. Clinical Trial.
-
Cardiovascular Risk/Benefit Profile of MHT.Medicina (Kaunas). 2019 Sep 6;55(9):571. doi: 10.3390/medicina55090571. Medicina (Kaunas). 2019. PMID: 31500138 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous