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Early prediction of preeclampsia in pregnancy with cell-free RNA.
Moufarrej, Mira N; Vorperian, Sevahn K; Wong, Ronald J; Campos, Ana A; Quaintance, Cecele C; Sit, Rene V; Tan, Michelle; Detweiler, Angela M; Mekonen, Honey; Neff, Norma F; Baruch-Gravett, Courtney; Litch, James A; Druzin, Maurice L; Winn, Virginia D; Shaw, Gary M; Stevenson, David K; Quake, Stephen R.
Afiliação
  • Moufarrej MN; Department of Bioengineering, Stanford University, Stanford, CA, USA.
  • Vorperian SK; ChEM-H and Department of Chemical Engineering, Stanford University, Stanford, CA, USA.
  • Wong RJ; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
  • Campos AA; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
  • Quaintance CC; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
  • Sit RV; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Tan M; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Detweiler AM; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Mekonen H; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Neff NF; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Baruch-Gravett C; Global Alliance to Prevent Prematurity and Stillbirth (GAPPS), Lynnwood, WA, USA.
  • Litch JA; Global Alliance to Prevent Prematurity and Stillbirth (GAPPS), Lynnwood, WA, USA.
  • Druzin ML; Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA.
  • Winn VD; Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA.
  • Shaw GM; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
  • Stevenson DK; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
  • Quake SR; Department of Bioengineering, Stanford University, Stanford, CA, USA. steve@quake-lab.org.
Nature ; 602(7898): 689-694, 2022 02.
Article em En | MEDLINE | ID: mdl-35140405
Liquid biopsies that measure circulating cell-free RNA (cfRNA) offer an opportunity to study the development of pregnancy-related complications in a non-invasive manner and to bridge gaps in clinical care1-4. Here we used 404 blood samples from 199 pregnant mothers to identify and validate cfRNA transcriptomic changes that are associated with preeclampsia, a multi-organ syndrome that is the second largest cause of maternal death globally5. We find that changes in cfRNA gene expression between normotensive and preeclamptic mothers are marked and stable early in gestation, well before the onset of symptoms. These changes are enriched for genes specific to neuromuscular, endothelial and immune cell types and tissues that reflect key aspects of preeclampsia physiology6-9, suggest new hypotheses for disease progression and correlate with maternal organ health. This enabled the identification and independent validation of a panel of 18 genes that when measured between 5 and 16 weeks of gestation can form the basis of a liquid biopsy test that would identify mothers at risk of preeclampsia long before clinical symptoms manifest themselves. Tests based on these observations could help predict and manage who is at risk for preeclampsia-an important objective for obstetric care10,11.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / RNA / Diagnóstico Precoce / Ácidos Nucleicos Livres Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / RNA / Diagnóstico Precoce / Ácidos Nucleicos Livres Idioma: En Ano de publicação: 2022 Tipo de documento: Article