MedPath

Measuring sVAP-1 as a Predictor of Pregnancy Problems

Terminated
Conditions
Pregnancy Complications
Interventions
Diagnostic Test: Blood test for soluble VAP-1 (sVAP-1).
Registration Number
NCT04891315
Lead Sponsor
University of Leicester
Brief Summary

Pre-eclampsia is a common pregnancy disorder defined as high blood pressure and protein in the urine after 20 weeks of pregnancy. It affects the function of the placenta and can cause severe complications, e.g, stroke, multiple organ damage and seizures for the mother, and fetal growth restriction or stillbirth for the baby. Pre-eclampsia can also cause long term health problems for mother and baby.

Currently, there is no test that can predict whether someone will develop pre-eclampsia, so nothing is done to intervene before the problems begin.

Results from their previous work suggest that the investigators may have found something that can be measured in a blood sample that can predict which women might develop pre-eclampsia. It is a protein known as Vascular Adhesion Protein-1 (VAP-1), and our evidence points at it being involved in the embryo attaching to the womb and also in helping the development of the placenta by helping to get the right cells to where they are needed.

The investigators will test blood samples from 451 pregnant women who come to the Leicester Royal Infirmary for routine bloods and their first pregnancy dating scan. The investigators will then follow the outcomes of the pregnancy to see if VAP-1 in the blood of women who develop pre-eclampsia (or other pregnancy complications) is different from the ones who do not develop pregnancy complications. The ability to predict women at higher risk of pregnancy complications would ensure the application of timely interventions and appropriate management of the conditions that may help to prevent complications both during pregnancy and later life.

The study is expected to last approximately 30 weeks and the participants will be asked to give one extra tube of blood whilst having their routine bloods taken and to also consent to follow up of medical records until the end of the pregnancy.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
102
Inclusion Criteria
  • Female participants who are in early pregnancy (<20 weeks gestational age).
  • 16 years and above
  • Patient consents to take part in the study
Read More
Exclusion Criteria
  • Patient declines to be involved in the study
  • Unsuccessful venepuncture
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Pregnant womenBlood test for soluble VAP-1 (sVAP-1).Women aged 16+ in early pregnancy (before 20 weeks of gestation).
Primary Outcome Measures
NameTimeMethod
Correlation of sVAP-1 levels with pregnancy complications: Gestational diabetes.During pregnancy up to 42 weeks

Diagnosis of gestational diabetes defined as:

A fasting plasma glucose level of 5.6 mmol/litre or above or A 2-hour plasma glucose level of 7.8 mmol/litre or above

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with Fetal outcomes: Fetal growth restrictionDuring pregnancy up to 42 weeks

Fetal growth restriction will be defined as:

Estimated fetal weight \>10th centile for gestational age.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with pregnancy complications: hypertension in pregnancyDuring pregnancy up to 42 weeks

Diagnosis of hypertension in pregnancy defined as:

Systolic BP ≥ 140 mm Hg or diastolic BP ≥ 90 mmHg.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with Fetal outcomes: StillbirthDuring pregnancy from 24 to 42 weeks

Stillbirths will be defined as:

The death of a baby before or during birth after 24 weeks of gestation.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with Fetal outcomes: Fetal macrosomiaDuring pregnancy up to 42 weeks

Fetal macrosomia,will be defined as:

Estimated fetal weight \>90th centile for gestational age.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with Fetal outcomes: MiscarriageDuring pregnancy up to 24 weeks

Miscarriage will be defined as:

Occurrence of spontaneous abortion \<24 weeks' gestation.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with pregnancy complications: Pre-eclampsiaDuring pregnancy up to 42 weeks

Diagnosis of pre-eclampsia defined as:

New-onset hypertension (\>140 mm Hg systolic or \>90 mm Hg diastolic) after 20 weeks of pregnancy and the coexistence of one or both of the following new-onset conditions:

Proteinuria (urine protein:creatinine ratio ≥30 mg/mmol, or albumin:creatinine ratio ≥8 mg/mmol, or ≥1 g/L \[2+\] on dipstick testing) Other maternal organ dysfunction.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with Fetal outcomes: Preterm labourDuring pregnancy up to 37 weeks

Preterm labour be defined as:

Birth \<37 weeks.

sVAP-1 levels will be measured by ELISA

Secondary Outcome Measures
NameTimeMethod
Correlation of sVAP-1 levels with patient characteristics: Smoking statusDuring pregnancy up to 42 weeks

Smoking status will be recorded as current/ex/never.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: WeightDuring pregnancy up to 42 weeks

Weight will be measured in kilograms.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: BMIDuring pregnancy up to 42 weeks

Weight and height will be combined to report BMI in kg/m\^2.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: Pre-existing medical conditionsAt time of recruitment

Pre-existing medical conditions will be recorded as reported on the patient's medical records.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: Medications at time of bookingAt time of recruitment

Medications at time of booking will be recorded as reported on the patient's medical records.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: Gestation at time of recruitmentAt time of recruitment

Gestation at time of recruitment will be measured in weeks.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: GravidityAt time of recruitment

Gravidity will be recorded as the total number of pregnancies.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: ParityAt time of recruitment

Parity will be recorded as the number of births with a gestational age of 24 weeks.

sVAP-1 levels will be measured by ELISA.

Correlation of sVAP-1 levels with patient characteristics: AgeAt time of recruitment

Age will be measured in years.

sVAP-1 levels will be measured by ELISA

Correlation of sVAP-1 levels with patient characteristics: EthnicityAt time of recruitment

Ethnicity will be recorded as described on the medical records of the patient.

sVAP-1 levels will be measured by ELISA.

Trial Locations

Locations (1)

Leicester Royal Infirmary

🇬🇧

Leicester, United Kingdom

© Copyright 2025. All Rights Reserved by MedPath