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Lipid profile of circulating placental extracellular vesicles during pregnancy identifies foetal growth restriction risk.
Klemetti, Miira M; Pettersson, Ante B V; Ahmad Khan, Aafaque; Ermini, Leonardo; Porter, Tyler R; Litvack, Michael L; Alahari, Sruthi; Zamudio, Stacy; Illsley, Nicholas P; Röst, Hannes; Post, Martin; Caniggia, Isabella.
Affiliation
  • Klemetti MM; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Pettersson ABV; Department of Obstetrics & Gynecology, University of Toronto, Toronto, Ontario, Canada.
  • Ahmad Khan A; Program in Translational Medicine, Peter Gilgan Centre for Research and Learning, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Ermini L; Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Canada.
  • Porter TR; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Litvack ML; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Alahari S; Program in Translational Medicine, Peter Gilgan Centre for Research and Learning, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Zamudio S; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Illsley NP; Placental Research Group LLC, Maplewood, New Jersey, USA.
  • Röst H; Placental Research Group LLC, Maplewood, New Jersey, USA.
  • Post M; Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Canada.
  • Caniggia I; Program in Translational Medicine, Peter Gilgan Centre for Research and Learning, Hospital for Sick Children, Toronto, Ontario, Canada.
J Extracell Vesicles ; 13(2): e12413, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38353485
ABSTRACT
Small-for-gestational age (SGA) neonates exhibit increased perinatal morbidity and mortality, and a greater risk of developing chronic diseases in adulthood. Currently, no effective maternal blood-based screening methods for determining SGA risk are available. We used a high-resolution MS/MSALL shotgun lipidomic approach to explore the lipid profiles of small extracellular vesicles (sEV) released from the placenta into the circulation of pregnant individuals. Samples were acquired from 195 normal and 41 SGA pregnancies. Lipid profiles were determined serially across pregnancy. We identified specific lipid signatures of placental sEVs that define the trajectory of a normal pregnancy and their changes occurring in relation to maternal characteristics (parity and ethnicity) and birthweight centile. We constructed a multivariate model demonstrating that specific lipid features of circulating placental sEVs, particularly during early gestation, are highly predictive of SGA infants. Lipidomic-based biomarker development promises to improve the early detection of pregnancies at risk of developing SGA, an unmet clinical need in obstetrics.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fetal Growth Retardation / Extracellular Vesicles Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Female / Humans / Newborn / Pregnancy Language: En Journal: J Extracell Vesicles Year: 2024 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fetal Growth Retardation / Extracellular Vesicles Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Female / Humans / Newborn / Pregnancy Language: En Journal: J Extracell Vesicles Year: 2024 Document type: Article Affiliation country: Canada
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