RNA profiles reveal signatures of future health and disease in pregnancy

Morten Rasmussen(University of California System), Mitsu Reddy(AbbVie (United States)), Rory Nolan(AbbVie (United States)), Joan Camuñas-Soler(AbbVie (United States)), Arkady Khodursky(AbbVie (United States)), Nikolai Madrid Scheller(Statens Serum Institut), David E. Cantonwine(Brigham and Women's Hospital), Line Engelbrechtsen(Herlev Hospital), Jia Mi(St Thomas' Hospital), Arup Dutta, Tiffany Brundage(AbbVie (United States)), Farooq Siddiqui(AbbVie (United States)), Mainou Thao(AbbVie (United States)), Elaine P.S. Gee(AbbVie (United States)), Johnny La(AbbVie (United States)), Courtney Baruch-Gravett(Global Alliance to Prevent Prematurity and Stillbirth), Mark K. Santillan(University of Iowa Hospitals and Clinics), Saikat Deb(Public Health Laboratory Ivo de Carneri), Shaali M. Ame(Public Health Laboratory Ivo de Carneri), Said M. Ali(Public Health Laboratory Ivo de Carneri), Melanie Adkins(Michigan State University), Mark A. DePristo(College of San Mateo), Manfred Lee(AbbVie (United States)), Eugeni Namsaraev(AbbVie (United States)), Dorte Jensen Gybel-Brask(Herlev Hospital), Lillian Skibsted(Zealand University Hospital), James A. Litch(Global Alliance to Prevent Prematurity and Stillbirth), Donna A. Santillan(University of Iowa Hospitals and Clinics), Sunil Sazawal, Rachel M. Tribe(St Thomas' Hospital), James M. Roberts(University of Pittsburgh), Maneesh Jain(AbbVie (United States)), Estrid Høgdall(Herlev Hospital), Claudia Holzman(Michigan State University), Stephen R. Quake(Chan Zuckerberg Initiative (United States)), Michal A. Elovitz(University of California System), Thomas F. McElrath(Brigham and Women's Hospital)
Nature
January 5, 2022
Cited by 194Open Access
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Abstract

Abstract Maternal morbidity and mortality continue to rise, and pre-eclampsia is a major driver of this burden 1 . 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 2 . 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.


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