» Articles » PMID: 34987224

RNA Profiles Reveal Signatures of Future Health and Disease in Pregnancy

Abstract

Maternal morbidity and mortality continue to rise, and pre-eclampsia is a major driver of this burden. Yet the ability to assess underlying pathophysiology before clinical presentation to enable identification of pregnancies at risk remains elusive. Here we demonstrate the ability of plasma cell-free RNA (cfRNA) to reveal patterns of normal pregnancy progression and determine the risk of developing pre-eclampsia months before clinical presentation. Our results centre on comprehensive transcriptome data from eight independent prospectively collected cohorts comprising 1,840 racially diverse pregnancies and retrospective analysis of 2,539 banked plasma samples. The pre-eclampsia data include 524 samples (72 cases and 452 non-cases) from two diverse independent cohorts collected 14.5 weeks (s.d., 4.5 weeks) before delivery. We show that cfRNA signatures from a single blood draw can track pregnancy progression at the placental, maternal and fetal levels and can robustly predict pre-eclampsia, with a sensitivity of 75% and a positive predictive value of 32.3% (s.d., 3%), which is superior to the state-of-the-art method. cfRNA signatures of normal pregnancy progression and pre-eclampsia are independent of clinical factors, such as maternal age, body mass index and race, which cumulatively account for less than 1% of model variance. Further, the cfRNA signature for pre-eclampsia contains gene features linked to biological processes implicated in the underlying pathophysiology of pre-eclampsia.

Citing Articles

A Comparison of Apelin Rs56204867 and Apelin Receptor Rs11544374 Gene Polymorphisms and Their Association with Risk of Preeclampsia in Southeast Iran.

Juybar M, Shahraki M, Ghasemi M, Payandeh A, Saljooghi S, Saravani M Rep Biochem Mol Biol. 2025; 13(2):273-280.

PMID: 39995647 PMC: 11847591. DOI: 10.61186/rbmb.13.2.273.


Leveraging Machine Learning to Predict and Assess Disparities in Severe Maternal Morbidity in Maryland.

Li Q, Alfonso Y, Wolfson C, Aziz K, Creanga A Healthcare (Basel). 2025; 13(3).

PMID: 39942473 PMC: 11817442. DOI: 10.3390/healthcare13030284.


Immune changes in pregnancy: associations with pre-existing conditions and obstetrical complications at the 20th gestational week-a prospective cohort study.

Westergaard D, Lundgaard A, Vomstein K, Fich L, Hviid K, Egerup P BMC Med. 2024; 22(1):583.

PMID: 39696496 PMC: 11657209. DOI: 10.1186/s12916-024-03797-y.


Advancing diagnosis and early risk assessment of preeclampsia through noninvasive cell-free DNA methylation profiling.

Baetens M, Van Gaever B, Deblaere S, De Koker A, Meuris L, Callewaert N Clin Epigenetics. 2024; 16(1):182.

PMID: 39695764 PMC: 11656954. DOI: 10.1186/s13148-024-01798-5.


Early prediction of preeclampsia using the first trimester vaginal microbiome.

Kindschuh W, Austin G, Meydan Y, Park H, Urban J, Watters E bioRxiv. 2024; .

PMID: 39677801 PMC: 11642775. DOI: 10.1101/2024.12.01.626267.


References
1.
Rich-Edwards J, Fraser A, Lawlor D, Catov J . Pregnancy characteristics and women's future cardiovascular health: an underused opportunity to improve women's health?. Epidemiol Rev. 2013; 36:57-70. PMC: 3873841. DOI: 10.1093/epirev/mxt006. View

2.
Tan M, Syngelaki A, Poon L, Rolnik D, OGorman N, Delgado J . Screening for pre-eclampsia by maternal factors and biomarkers at 11-13 weeks' gestation. Ultrasound Obstet Gynecol. 2018; 52(2):186-195. DOI: 10.1002/uog.19112. View

3.
Marinic M, Lynch V . Relaxed constraint and functional divergence of the progesterone receptor (PGR) in the human stem-lineage. PLoS Genet. 2020; 16(4):e1008666. PMC: 7190170. DOI: 10.1371/journal.pgen.1008666. View

4.
Robillard P, Dekker G, Hulsey T . Evolutionary adaptations to pre-eclampsia/eclampsia in humans: low fecundability rate, loss of oestrus, prohibitions of incest and systematic polyandry. Am J Reprod Immunol. 2002; 47(2):104-11. DOI: 10.1034/j.1600-0897.2002.1o043.x. View

5.
McCarthy F, Kingdom J, Kenny L, Walsh S . Animal models of preeclampsia; uses and limitations. Placenta. 2011; 32(6):413-9. DOI: 10.1016/j.placenta.2011.03.010. View