Effect of Hormone Replacement Therapy on the
Cardiovascular System
Fait T.1, Málková J.2, Živný J.1
1Gynekologicko-porodnická klinika, UK, 1. LF a VFN Praha, přednosta prof. MUDr. J. Živný, DrSc. 2III. interní – kardiologická klinika FNKV, přednosta prof. MUDr. P.Widimský, DrSc. |
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Summary:
Objective: Analysis of contemporary knowledge of influences of hormone replacement therapy on
cardiovascular system.
Design: Literary review.
Setting: Department of Gynecology and Obstetrics, 1th Faculty of Medicine, Charles University,
Prague.
Method: Informations were collected from fulltexts which were chosen in database Medline and
Ovid.
Conclusion: Hormone replacement therapy (HRT) has positive influence on some risk factors of
cardiovascular disease. Changes in the lipoprotein spectrum are well known.
Oral estrogens cause a decrease of low density lipoprotein cholesterol (LDL-C) and, especially an
increase of high density lipoprotein cholesterol (HDL-C) levels, which both have potentially favourable
effects; they also cause a triglyceride level increase, which probably has no clinical
relevance except in cases with basal hypertriglyceridemia. Transdermal estradiol causes generally
a minor dicrease in LDL-C and minor increase HDL-C levels, with no increase or even decrease
in triglyceride levels. The addition of androgenic progestins at conventionally used doses, while
not interfering with LDL-C variations, causes a HDL-C decrease, which contrasts he effect of oral
estrogens and completely reverses the effect of transdermal estradiol. On the contrary, the addition
of a non-adrogenic progestin does not interfere with any of the estrogen induced lipid profile
modifications.
Transdermal estradiol does not cause change of insulinoresistance. Estrogen substitution protects
gynoid distribution of body fat that is conected with lower risk of ischemic heart disease.
Estrogens have posibility to dilate vessels. Decreasing of levels of cytoadhesive moleculs was
verificate during HRT so as lowering of homocysteine level to premenopausal levels.
Newly uncovered changes like the significant increase of CRP conected with oral estrogene
therapy could explain increasing of cardiovascular risk on the beginning of HRT especially in
group of women with history of ischemic heart disease.
Key words:
hormone replacement therapy, cardiovascular disease
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