Changes of hsCRP Levels Induced by Different Application Ways of Estrogene
Replacement Therapy
Fait T., 1Vrablík M., 2Koštířová M., 2Trnková B.
Gynekologicko-porodnická klinika 1. LF UK a VFN, Praha 1III. interní klinika 1. LF UK a VFN, Praha 2Ústav klinické biochemie l. LF UK a VFN, Praha |
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Summary:
Background. C-reactive protein is one of the independent risk factors of cardiovascular diseases. The aim of study
was to find changes of hsCRP levels during transdermal and oral application of estrogen replacement therapy.
Methods and Results. Two application ways were used for 12 weeks: oral estradiol 2 mg/day and transdermal
estradiol 50 μg /day (7-day patches). 41 healthy women with average age 49±6 years were randomised into
prospective cross-over designed study. The average level of hsCRP before therapy was 3,3 mg/l. Elevation on 4,8 mg/l
after the oral therapy was significant (p=0,05). Transdermal estrogene therapy did not induce any significant (p=0,87)
changes. Differences between oral and transdermal therapy were significant (p=0,002).
Conclusions. The transdermal application of the estrogene replacement therapy is more safety for a vessel wall from
the view of hsCRP levels. Differences between transdermal and oral application way are apparent even in case of the
early start of hormone replacement therapy.
Key words:
hormone replacement therapy, high sensitive C-reactive protein, cardiovascular diseases.
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