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Published on: August 13, 2019
Post-menopausal hormone therapy and concentrations of protein C and antithrombin in elderly women
M Cushman1, B M Psaty, E N Meilahn
1Department of Medicine, University of Vermont, Burlington, VT, USA. mcushman@salus.uvm.edu
Insights
Hormone therapy (HRT) in elderly women impacts blood clotting proteins. Oestrogen increased protein C, while both HRT types lowered antithrombin, potentially increasing venous thrombosis risk.
Area of Science:
- Gerontology
- Cardiovascular Health
- Hematology
Background:
- Post-menopausal hormone therapy (HRT) effects on blood coagulation in elderly women remain unclear.
- Elderly women are at higher risk for venous thromboembolism.
Purpose of the Study:
- To investigate the association between HRT use and natural anticoagulant protein levels in women aged 65 and older.
- To determine if HRT influences protein C and antithrombin concentrations in this demographic.
Main Methods:
- Cross-sectional study of 3393 women from the Cardiovascular Health Study.
- Measured protein C antigen and antithrombin levels in HRT users (oestrogen-only and oestrogen/progestin) and non-users.
- Age- and race-matched comparison groups were used.
Main Results:
- Oestrogen therapy was linked to significantly higher protein C levels compared to non-users.
- Both oestrogen-only and oestrogen/progestin therapies were associated with lower antithrombin levels.
- HRT-associated antithrombin reduction was more pronounced in thinner Caucasian and Black women.
Conclusions:
- HRT may increase venous thrombosis risk in elderly women, potentially mediated by reduced antithrombin levels.
- Protein C levels do not appear to be a significant factor in HRT-related venous thrombosis.
- Further research is needed to explore HRT-induced changes in anticoagulant function and their relation to thrombosis occurrence.
Abstract:
The effects of post-menopausal hormone therapy (HRT) on blood coagulation in elderly women are not well defined. We studied associations of HRT use with levels of natural anticoagulant proteins in a cross-sectional study of 3393 women > or = 65 years of age participating in the Cardiovascular Health Study. Protein C antigen and antithrombin were measured in all users (n = 230 unopposed oestrogen; 60 oestrogen/progestin) and a comparison group of 196 age- and race-matched non-users. Compared with non-users, oestrogen use was associated with higher protein C (4.80 vs. 4.30 microg/ml, P < 0.01). Results were similar for oestrogen/progestin (P > 0.05). In both user groups, antithrombin was lower than in non-users (109% for each vs. 115% in non-users, P < 0.001). Adjustment for factors related to prescription of HRT and to anticoagulant protein levels had little impact on the results. For antithrombin, associations with HRT were larger for thinner Caucasian women and black women. Venous thrombosis from HRT may be mediated partly by alterations in antithrombin, but not protein C concentrations. This study extends previous observations to older women, the group at highest risk of venous thromboembolism. Studies of HRT-induced alterations in anticoagulant function in relation to the occurrence of thrombosis with HRT are required.
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