Preeclampsia (PE)
Conditions
Keywords
Early Screening, First Trimester Diagnostic, Cell-Free RNA (cfRNA), Molecular Profile, Blood Biomarkers
Brief summary
Preeclampsia (PE) is a major obstetric complication with severe short- and long-term consequences for both mother and fetus. Early detection is critical to mitigate PE-related morbidity and mortality. Effective screening tools are needed to identify women at risk, enabling timely preventive and therapeutic interventions. Current screening methods primarily target placental biomarkers like sFLT1 and PlGF, which are limited to short-term predictions near symptom onset. Existing first-trimester assessments that incorporate maternal factors and Doppler metrics remain constrained by low sensitivity (\<41%) in compliance with NICE and ACOG guidelines. Recent advancements in cell free RNA (cf-RNA) analysis have revealed potential in first-trimester PE prediction. Findings from the PREMOM study (NCT04990141) established a molecular profile for early-onset preeclampsia (EOPE) and late-onset preeclampsia (LOPE) through cfRNA analysis, culminating in the development of the MaiRa Preeclampsia Test (Maternal Advanced and Innovative Preeclampsia Risk Assessment), which demonstrated high predictive performance for first- and second-trimester screening. The current study hypothesizes that the MaiRa Preeclampsia Test is generalizable, maintaining its predictive accuracy in an independent cohort.
Detailed description
This multicentre, prospective observational study aims to validate the MaiRa Preeclampsia Test, a molecular screening tool for predicting early-onset preeclampsia (EOPE) and late-onset preeclampsia (LOPE) in the first and second trimesters of pregnancy. The study will evaluate its diagnostic accuracy, including sensitivity, specificity, predictive values, and area under the curve (AUC). Study Design: Duration: 40 months * Recruitment and Sample Collection: 28 months * Sample Analysis: 32 months * Follow-Up: 8 months * Statistical Analysis and Publication: 6 months Participants: 7,473 pregnant women from 12 tertiary hospitals in Spain. Visits: * Visit 1 (T1): 9-14 weeks' gestation (first blood sample) * Visit 2 (T2): 15-26 weeks' gestation (second blood sample) * Visit 3 (T3): ≥27 weeks' gestation (third blood sample) Blood samples will be analyzed using the MaiRa Preeclampsia Test, with results correlated against obstetric outcomes as the gold standard. Data will be documented in an electronic Case Report Form (eCRF). Quality assurance will be maintained via continuous data monitoring and verification.
Interventions
PROCEDUREPeripheral blood collection
Maternal peripheral blood will be collected 3 times during pregnancy (1st, 2nd and 3rd trimester) and clinical data will also be compiled.
Sponsors
iPremom
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Signed informed consent approved by the Ethics Committee. * Women ≥18 years of age at consent. * Single gestation pregnancies with first sample collection (T1) possible between 9 and 14 weeks' gestation.
Exclusion criteria
* Active neoplasm. * History of organ or bone marrow transplantation. * Maternal transfusion within 8 weeks before sample collection. * Evidence of early pregnancy loss at consent. * Severe, uncontrolled infections. * Other investigator-assessed risks that could compromise participation or data quality.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Validation of the MaiRa Preeclampsia Test for first-trimester screening (9-14 weeks) of EOPE | From the date of enrollment (minimum 9 weeks) until the end of pregnancy (maximum 43 weeks), assessed up to 34 weeks. | Sensitivity, specificity, accuracy, F1-score, positive/negative predictive values, false discovery rate, AUC. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Validation of second-trimester screening (15-26 weeks) for EOPE | From the date of enrollment (minimum 9 weeks) until the end of pregnancy (maximum 43 weeks), assessed up to 34 weeks. | Sensitivity, specificity, accuracy, F1-score, positive/negative predictive values, false discovery rate, AUC. |
| Validation of second-trimester screening (15-26 weeks) for LOPE | From the date of enrollment (minimum 9 weeks) until the end of pregnancy (maximum 43 weeks), assessed up to 34 weeks. | Sensitivity, specificity, accuracy, F1-score, positive/negative predictive values, false discovery rate, AUC. |
Countries
Spain
Contacts
CONTACTClinical Studies Department
CONTACTÉrika Ortiz Domingo
PRINCIPAL_INVESTIGATORCarlos Simón, MD, PhD
Carlos Simon Foundation
PRINCIPAL_INVESTIGATORTamara Garrido, PhD
iPremom
Outcome results
None listed