Related Experiment Videos
Hormone therapy affects plasma measures of factor VII-activating protease in younger postmenopausal women
J J Sidelmann1, S O Skouby, F Vitzthum
1Unit for Thrombosis Research, Institute of Public Health, University of Southern Denmark, Niels Bohrs Vej 9, Esbjerg, Denmark.
Insights
Hormone therapy (HT) increases Factor VII-activating protease (FSAP) levels in postmenopausal women. This rise may explain HT's protective role in coronary heart disease (CHD) for younger women.
Area of Science:
- Cardiovascular Science
- Endocrinology
- Biochemistry
Background:
- Hormone therapy (HT) shows varied effects on coronary heart disease (CHD) risk in postmenopausal women, potentially protective in younger individuals but detrimental in older ones.
- Factor VII-activating protease (FSAP), a serine protease found in atherosclerotic plaques, is implicated in plaque stability and CHD development.
- Reduced plasma FSAP levels may correlate with atherosclerosis progression and CHD precipitation.
Purpose of the Study:
- To investigate the influence of different hormone therapy (HT) regimens on plasma levels of Factor VII-activating protease (FSAP) in postmenopausal women.
- To determine if HT affects FSAP antigen, activity, and ratio over a 1-year treatment period.
Main Methods:
- A study involving 139 postmenopausal women allocated to five HT groups and a control group.
- Blood samples collected at baseline and after 12 months of treatment.
- Assays used to measure FSAP antigen and FSAP activity.
Main Results:
- No significant changes in FSAP measures were observed in the control group after 12 months.
- Hormone therapy (HT) significantly increased FSAP antigen, FSAP activity, and the FSAP ratio in treated postmenopausal women.
- Specific increases noted: FSAP antigen (p=0.05), FSAP activity (p<0.001), and FSAP ratio (p=0.01) after 1 year of HT.
Conclusions:
- Hormone therapy (HT) demonstrably increases plasma FSAP measures in postmenopausal women.
- The observed increase in FSAP due to HT may contribute to the cardioprotective effects of HT in younger postmenopausal women.
Objectives:
Current reviews indicate that hormone therapy (HT) has a protective role in coronary heart disease (CHD) in younger postmenopausal women, whereas HT contributes to CHD in older women. Factor VII-activating protease (FSAP) is a serine protease that accumulates in unstable atherosclerotic plaques. FSAP is presumably involved in plaque stability and rupture. Reduced plasma concentration of FSAP may be associated with the development and expression of atherosclerosis and may thus contribute to precipitation of CHD. Here we address the potential influence of various HT regimens on plasma measures of FSAP in postmenopausal women treated for 1 year with different HT formulations or no HT.
Methods:
Six groups of postmenopausal women (n = 139) were allocated to five different HT modalities or no HT. Samples were collected at baseline and after 12 months of treatment. Prototype assays were used for the determination of FSAP antigen and FSAP activity.
Results:
The FSAP measures were comparable at baseline. No significant changes were observed in the control group after 12 months. HT in general induced a significant increase in FSAP antigen (7.7 microg/ml at baseline and 8.0 microg/ml after 12 months, p = 0.05), FSAP activity (1.54 PEU/ml at baseline and 1.68 PEU/ml after 12 months, p < 0.001) and FSAP ratio (202 mPEU/microg at baseline and 210 mPEU/microg after 12 months, p = 0.01).
Conclusions:
HT increases the plasma measures of FSAP. This increase may contribute to the protective effect on CHD induced by HT in younger postmenopausal women.
Related Concept Videos
Therapeutic Drug Monitoring: Affecting Factors
Venous Thrombosis III: Interprofessional Care
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Hormonal Regulation of the Menstrual Cycle
At puberty, GnRH begins a pulsatile release pattern, which triggers the anterior pituitary gland to secrete follicle-stimulating hormone (FSH) and luteinizing hormone (LH). The frequency and amplitude of GnRH pulses vary across the menstrual cycle, with faster pulses favoring LH release and slower pulses favoring FSH release.