The goal of this study is to understand whether statin therapy, a common lipid-lowering therapy, may improve the coagulation profile of menopausal women with hypercholesterolemia undergoing hormone replacement therapy with oral estroprogestin. It will also learn about the liver safety of the combination. The main questions will be: 1. does hormone replacement therapy affect the coagulation profile? 2. when we add statin therapy due to hypercholesterolemia not improving with lifestyle, does it reverse eventual changes of the coagulation profile occurred after initiation of hormone replacement therapy? 3. do the two therapies have an effect on overall inflammation of the organism? Participants will be asked to participate to the study before starting any therapy, if they need hormone relacement therapy due to symptoms, if they have a new onset of dyslipidemia and if they do not have contraindications to the therapies object of the study. The study is observational, thus it will not affect in any way the clinical care, which will follow only guidelines. During routine blood sample collection, additional aliquotes will be taken for the study at the recruitment, after 3 months of hormone replacement therapy and lifestyle changes, at the end of the study (after one year from the recruitment).
Study Type
OBSERVATIONAL
Enrollment
70
To be included in the study, patients must have menopausal symptoms requiring hormone replacement therapy without contraindications to it. All cohorts will undergo this therapy.
After 3 months, patients not controlling hypercholesterolemia with lifestyle changes will be prescribed statin as per clinical routine practice. They will be part of the HRT+statin cohort.
Santa Chiara Hospital - University Hospital of Pisa
Pisa, Italy, Italy
RECRUITINGHRT+Statin vs HRT only on the endogenous thrombin potential of the thrombin generation assay
Verify that the combination of statins and hormone replacement therapy (HRT) in symptomatic menopausal patients with cholesterol levels not at target induces an improvement in the venous thromboembolic (VTE) risk profile in terms of improvement in the endogenous thrombin potential (ETP) of the thrombin generation assay (TGA) compared to HRT alone.
Time frame: From 3 months to end of study (12 months)
HRT+Statin vs HRT only on the nAPCsr after TGA
Verify that the combination of statins and HRT can modify the normalized activated protein C sensitivity ratio compared to HRT alone.
Time frame: From 3 months to end of study (12 months)
HRT+statins vs HRT only do not increase liver transaminases
Verify that the combination of statins and HRT does not have a significant impact on liver function indices (AST, ALT, GGT, all in IU/L) compared to HRT alone.
Time frame: From 3 months to end of study (12 months)
HRT+statins vs HRT only on coagulation factors
Verify that the combination of statins and HRT can modify the expression of coagulation factors compared to HRT alone: * fibrinogen (mg/dl) * tissue factor (pg/mL) * thrombomodulin (ng/mL) * TFPI (ng/mL) * PAI-1 (ng/mL)
Time frame: From 3 months to end of study (12 months)
HRT+statins vs HRT only on inflammatory markers
Verify that the combination of statins and HRT can modify the expression of inflammatory indices compared to HRT alone: * IL1 (pg/mL) * IL6 (pg/mL) * TNFalpha (pg/mL)
Time frame: From 3 months to end of study (12 months)
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