Diagnostic Value of sFlt-1/PlGF Ratio for the Etiology of Intra Uterine Growth Restriction - ANGIOPAG

NCT ID: NCT05151289

Last Updated: 2021-12-09

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 152 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-01-08
• Study Completion Date: 2022-01-29

Brief Summary

The main aim of this project is to determine the Placental Growth Factor and Vascular Endothelial Growth Factor ratio's performance (sFlt-1/PlGF) for the etiological diagnosis of vascular Intrauterine growth restriction (IUGR) compared to a non-vascular IUGR.

Detailed Description

Intra-uterine growth restriction is one of the most frequent cause of consultation in prenatal diagnosis centers. Suspected Intrauterine growth restriction (IUGR) concerns 5.4% of pregnancies. Prognosis and management of IUGR depends on its etiology. It has been estimated that 80 to 90% of IUGR have a vascular cause, 5-15% an infectious cause and 2 to 5% chromosomal or genetic cause. More recently, a meta-analysis has shown that among 874 IUGR fetuses for whom amniocentesis was performed, anomaly of caryotype or comparative genomic hybridization array was reported for 6%. In case of vascular IUGR, amniocentesis is not indicated and close surveillance of mother and fetus is organized.

The diagnosis of vascular IUGR is most often confirmed after birth with placental histology. Before birth, the diagnosis of vascular IUGR is presumptive, and based on gestational age at diagnosis, quantity of amniotic fluid, end dopplers of umbilical artery and uterine arteries. The argument considered as most specific of vascular IUGR is the doppler of uterine arteries, however it has been shown that sensitivity of this test is weak : abnormal uterine arteries is reported in only 40% of fetuses with vasculat IUGR according to placenta pathology.

Biochemical markers Placental Growth Factor and Vascular Endothelial Growth Factor (sFlt1 and PlGF) have shown their prognostic value on the occurrence of preeclampsia. They are both associated to the delay until occurrence of preeclampsia and to the delay before extraction in case of IUGR. As diagnostic tool in IUGR, only two studies have investigated their value : the PlGF/sFlt-1 ratio identified 7 patients among 10 with abnormal placental pathology, and low PlGF value is associated with abnormal placental pathology among 122 cases of IUGR, however this study did not specify sensitivity and specificity values. A reliable and reproductible marker that could orient practitioners towards the need to propose amniocentesis at diagnosis of IUGR is therefore important to develop.

The main objective of ANGIOPAG is to determine the sFlt-1/PlGF ratio's performance for the etiological diagnosis of vascular IUGR compared to a non-vascular IUGR.

To reach this goal, ANGIOPAG is a diagnostic, multicenter, non-randomized study. It will be performed on 152 pregnant women over 18 with a term between 22and 34 +6 Weeks of Gestation (WG), consulting in participating centers for IUGR. For the research, a blood test will be carried, at the inclusion and 2 to 4 weeks after, to determine sFLT-1 and PlGF. All included patients'placenta will be analyzed, even in case of a child normal birth weight.

Conditions

Intrauterine Growth Restriction; Fetal Growth Restriction (FGR)

Keywords

sFlt1; PlGF; IUGR; intrauterine growth restriction; fetal growth restriction

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Patients consulting in one of the participating centers for intra uterine growth restriction.

All included patients

Group Type: EXPERIMENTAL

Blood test at time of inclusion for sFlt-1/PlGF ratio

Intervention Type: BIOLOGICAL

As part of the research, a blood sample is taken to measure the sFLT-1 and PlGF ratio at the inclusion visit.

Follow-up blood test 2 to 4 weeks after inclusion

Intervention Type: BIOLOGICAL

As part of the research, a blood sample is taken to measure the sFLT-1 and PlGF ratio at the follow-up visit (about 2-4 weeks after inclusion). This second sample is not mandatory for the evaluation of the study's main endpoint.

Placenta analysis for all included patients, even in case of normal birthweight

Intervention Type: DIAGNOSTIC_TEST

After delivery, the placenta of each included patient is sent to anatomo-pathology (even in case of normal weight of the baby at birth). An anatomopathologist referent, designated for the study in each center, performs an analysis (aware of the clinic but not of the sFLT-1/PlGF ratio results), according to the benchmark criteria grid. Local analysis will classify the placenta as "vascular IUGR" or "nonvascular IUGR".

Interventions

Blood test at time of inclusion for sFlt-1/PlGF ratio

As part of the research, a blood sample is taken to measure the sFLT-1 and PlGF ratio at the inclusion visit.

Intervention Type: BIOLOGICAL

Follow-up blood test 2 to 4 weeks after inclusion

As part of the research, a blood sample is taken to measure the sFLT-1 and PlGF ratio at the follow-up visit (about 2-4 weeks after inclusion). This second sample is not mandatory for the evaluation of the study's main endpoint.

Intervention Type: BIOLOGICAL

Placenta analysis for all included patients, even in case of normal birthweight

After delivery, the placenta of each included patient is sent to anatomo-pathology (even in case of normal weight of the baby at birth). An anatomopathologist referent, designated for the study in each center, performs an analysis (aware of the clinic but not of the sFLT-1/PlGF ratio results), according to the benchmark criteria grid. Local analysis will classify the placenta as "vascular IUGR" or "nonvascular IUGR".

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• > 18 years old
• Singleton pregnancy
• Date of conception evaluated by ultrasound < 14 WG
• Consulting in one of the 3 participating centers for IUGR
• Estimated fetal weight < 5th centile (according to Hadlock 3 et CFEF)
• Between 22+0 WG et 34+6 WG

Exclusion Criteria

• Major birth defect diagnosed at time of inclusion
• Abnormality of caryotype known at time of inclusion
• Confirmed preeclampsia at time of inclusion

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jeanne Sibiude, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Locations

Hôpital Louis Mourier

Colombes, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Jeanne Sibiude, MD, PhD

Role: CONTACT

Phone: 01 40 60 66 11

Email: jeanne.sibiude@aphp.fr

Facility Contacts

Jeanne Sibiude, MD, PhD

Role: primary

Other Identifiers

2019-A01116-51

Identifier Type: REGISTRY

Identifier Source: secondary_id

APHP190472

Identifier Type: -

Identifier Source: org_study_id