MedPath

Characterisation of lipoproteins from patients with preeclampsia compared to healthy, pregnant and healthy, non-pregnant wome

Conditions
Pre-eclampsia
preeclampsia
O14
Registration Number
DRKS00005368
Lead Sponsor
niversitätklinikum Freiburg Institut für Klinische Chemie und Laboratoriumsmedizin
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
155
Inclusion Criteria

Group 1 (case): Pregnant women with preeclampsia according to the criteria of the German Society of Gynaecology and Obstetrics: hyptertension in pregancy (RR>140/90mmHg) and proteinuria (>300 mg/24h) occuring after the 20th week of pregnancy. Preeclampsia can also be diagnosed without proteinuria if fetal growth restriction, liver involvement, renal insufficiency, neurological dysfunctions or hematological disorders are observed after the 20th week of pregnancy. Informed consent. Age >18 years. Group 2 (control): for every individual from group 1 a healthy, pregnant women in matching gestational age (+/- 1 week). Informed consent. Age > 18 years. Group 3 (control): Healthy, non pregnant women. Informed consent. Age > 18 years and < 45 years.

Exclusion Criteria

Group 1 (case): lack of informed consent. Group 2 and 3 (controls): lack of informed consent. By anamnesis detection of: arterial hypertension, treatment with antihypertensive agents and other cardiac drugs, diabetes mellitus, renal insufficiency, lipid disorders, liver diseases.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of lipidvalues from ultracentrifugation process and subsequent enzymatic measurement. Exploratory analysis of results, therefore no further specification of endpoints possible.
Secondary Outcome Measures
NameTimeMethod
Comparison of the influence of different lipoproteinfraction obtained from ultracentrifugation process on vasoactive receptors and their second messengers in cell culture models. Exploratory analysis of results, therefore no further specification of endpoints possible.
© Copyright 2025. All Rights Reserved by MedPath