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Menopause Related Influences on Leukocyte Distribution, Monocyte Function and Platelet Reactivity

Menopause Related Influences on Leukocyte Distribution, Monocyte Function and Platelet Reactivity

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05985447
Enrollment
180
Registered
2023-08-14
Start date
2022-03-07
Completion date
2026-12-31
Last updated
2023-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction, Arteriosclerosis, Cardiovascular Events, Menopause

Keywords

sex, gender, female, male, menopause, hormone replacement therapy, Atherosclerosis, cardiovascular events, cardiovascular risk

Brief summary

Women and men show marked differences in cardiovascular risk profile and outcome. Women experience fewer cardiovascular events than men before menopause, but this relationship seems to reverse at menopause. These disparities are probably due to hormonal factors, especially the female sex hormone estrogen seems to have a protective influence on the development of atherosclerotic plaques premenopausal. The underlying mechanisms of the effect of estrogens on the vessel wall are still insufficiently investigated. In this study, menopause related effects on leukocyte distribution and function as well on platelets and their aggregational response will be evaluated.

Detailed description

Sex-specific differences in the risk profile and outcome of cardiovascular diseases are evident, which are probably due to hormonal factors. Women suffer significantly fewer cardiovascular events than men before menopause, after menopause this relationship seems to reverse. Moreover, outcome is worse in female patients compared to men. Platelets and leukocytes play an essential role in cardiovascular risk. Nevertheless, the underlying mechanisms of the mechanistic effects of the hormone transition in menopause on leukocytes and platelets have only been insufficiently investigated so far. Moreover, effects of a possible hormone replacement therapy are insufficiently understood with contradictive literature concerning cardiovascular effects. The aim in this study, is to analyse leukocyte and platelet function in dependence from menopause related changes in hormone levels of estrogen, testosterone, progesterone, LH and FSH. Moreover, hormone replacement therapy will be investigated. For this purpose, blood samples from male and female patients will be investigated with regard to age and menopause status. The blood samples are analysed by FACS to differentiate the leukocytes and test for inflammatory properties and reactive oxygen species. The monocyte distribution divided according to the surface markers CD14 and CD16 is analysed. In addition, plasma from the patient samples will be used to assess hormone levels in the blood. In addition, patient data such as general laboratory parameters, risk and lifestyle factors are collected and associated with the hormone and lipid levels. For platelet function analysis, light-transmittance aggregometry, flow cytometry (platelet leukocyte crosstalk, investigation of platelet surface markers for platelet activation and cell-cell-adhesion) will be investigated. Platelets secretory potency will be analysed by ATP-release. Moreover, platelet adhesion will be investigated by collagen-coated flow chambers. Platelet proteomics and RNA sequencing will complement the data in an unbiased approach. In addition in-vitro incubation analyses with estrogen and testosterone will be conducted to investigate hormone replacement therapy effects.

Interventions

None listed

Sponsors

Heinrich-Heine University, Duesseldorf
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age \> 18 years * Male, female, diverse patients with current treatment in the Department of Cardiology, Pneumology and Angiology. * Persons who are able to understand and follow the instructions of the study staff * Written informed consent

Exclusion criteria

* Age \< 18 years * Lack of written consent to participate in the study * coagulation disorders

Design outcomes

Primary

MeasureTime frameDescription
Leukocyte distribution measured by flow cytometrysingle time, up to one day after inclusionCD45 (Leukocytes), CD3 (T-cells), CD14 (Monocytes), CD16 (Granulocytes), CD19 (B-cells)
Platelet functionsingle time, up to one day after inclusionmeasured by light transmittance aggregometry (Parameters: Maximum of Aggregation, Slope
Platelet surface markers, platelet leukocyte crosstalk (CD40, CD40L)single time, up to one day after inclusionmeasured by flow cytometry (FACS)

Secondary

MeasureTime frameDescription
Hormone levels of progesteronesingle time, up to one day after inclusionmeasured by ELISA \[µg/l\]
Hormone levels of follicle stimulating hormonesingle time, up to one day after inclusionmeasured by ELISA \[µg/l\]
Reactive Oxygen Species (ROS) Generation via CellRoxGreen [geometric mean]single time, up to one day after inclusionmeasured by Flow Cytometry (FACS)
Questionnaire including lifestyle factors, cardiovascular risk factorssingle time, up to one day after inclusion
Hormone levels of luteinizing hormonesingle time, up to one day after inclusionmeasured by ELISA \[µg/l\]
Hormone levels of estrogensingle time, up to one day after inclusionmeasured by ELISA \[ng/l\]
Hormone levels of testosterone measured by ELISAsingle time, up to one day after inclusionmeasured by ELISA \[ng/l\]

Countries

Germany

Contacts

Primary ContactLisa Dannenberg, MD
lisa.dannenberg@med.uni-duesseldorf.de+492118105315

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026