Polygenic Risk Scores for Preeclampsia Prediction Beyond Gold-Standard Clinical Models in Multiethnic Populations

Maddalena Ardissino1,2,3,4, Kypros Nicolaides4,5, Frances Conti-Ramsden4

  • 1Medical Research Council, Laboratory of Medical Sciences Imperial College London UK.

Insights

Polygenic risk scores (PRS) offer modest improvement for predicting preeclampsia in European ancestry women. Their utility is limited in African ancestry women due to underrepresentation in genetic studies, highlighting a need for equitable development.

Area of Science:

  • Genetics and Genomics
  • Maternal-Fetal Medicine
  • Reproductive Health

Background:

  • Preeclampsia poses significant risks to maternal and fetal well-being.
  • Early identification of high-risk pregnancies is crucial for implementing preventative measures.
  • The predictive value of polygenic risk scores (PRS) for preeclampsia requires further investigation, especially across diverse ancestries.

Purpose of the Study:

  • To evaluate the added predictive value of preeclampsia and systolic blood pressure PRS in first-trimester prediction models.
  • To compare PRS performance against established clinical and advanced prediction models.
  • To assess PRS performance across different ancestral groups.

Main Methods:

  • Two prospective pregnancy cohorts (Fetal Medicine Foundation and Pregnancy Outcome Prediction studies) were analyzed.
  • Risk models incorporated clinical factors, PRS, and advanced first-trimester markers (mean arterial pressure, PAPP-A, uterine artery pulsatility index).
  • Discriminative performance was measured using the area under the receiver operating characteristic curve (AUC) and assessed by ancestry.

Main Results:

  • Preeclampsia PRS showed independent association with preeclampsia, modestly improving prediction over clinical models (AUC 0.746 vs. 0.750).
  • No significant improvement was observed when PRS were added to the advanced model (AUC 0.817 vs. 0.818).
  • Systolic blood pressure PRS improved prediction in European ancestry women but not in African ancestry women.

Conclusions:

  • PRS for preeclampsia and systolic blood pressure offer limited additional predictive value beyond clinical factors in European ancestry women.
  • Underrepresentation in genome-wide association studies limits the utility of current PRS in African ancestry populations.
  • Refined PRS models and larger cohorts may enhance equitable risk stratification in maternal health in the future.
Abstract

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