Classification of preeclampsia according to molecular clusters with the goal of achieving personalized prevention

Than, Nándor Gábor ✉ [Than, Nándor Gábor (Rendszerbiológia), author] Institute of Enzymology (RCNS); Enzim_416 (IMLS); Department of Obsterics and Gynecology Baross S... (SU / FM / C / DOG); Romero, Roberto; Posta, Máté [Posta, Máté (Szülészet- és nőg...), author] Enzim_416 (IMLS); School of PhD Studies (SU); Györffy, Dániel [Györffy, Dániel (Bioinformatika), author] Institute of Enzymology (RCNS); Információs Technológiai és Bionikai Kar (PPCU); Szalai, Gábor [Szalai, Gábor (Radiológia), author] Surgery Clinic (UP / UPMS); Rossi, Simona W; Szilágyi, András [Szilágyi, András (Bioinformatika), author] Institute of Enzymology (RCNS); Enzim_416 (IMLS); Hupuczi, Petronella [Hupuczi, Petronella (Aneszteziológia é...), author] Department of Anesthesoiology and Intensiv Therapy (SU / FM / C); Nagy, Sándor [Nagy, Sándor (szülészet-nőgyógy...), author] Faculty of Health and Sport Sciences; Department of Obstetrics and Gynecology (FHSS); Török, Olga [Török, Olga (szülészet-nőgyógy...), author] Department of Obstetrics and Gynecology (UD); Tarca, Adi L; Erez, Offer; Ács, Nándor [Ács, Nándor (Szülészet-nőgyógy...), author] Department of Obsterics and Gynecology Üllői St... (SU / FM / C / DOG); Papp, Zoltán [Papp, Zoltán (Szülészet-nőgyógy...), author] Department of Obsterics and Gynecology Baross S... (SU / FM / C / DOG)

English Survey paper (Journal Article) Scientific
Published: JOURNAL OF REPRODUCTIVE IMMUNOLOGY 0165-0378 1872-7603 161 Paper: 104172 , 8 p. 2024
  • SJR Scopus - Immunology: Q2
Identifiers
Fundings:
  • (GINOP-2.1.7-15-2016-00415)
  • (K128262)
  • Piacvezérelt kutatás-fejlesztési és innovációs projektek támogatása(2020-1.1.2-PIACI-KFI-2021-00273) Funder: Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal
  • (2020-1.1.5-GYORSÍTÓSÁV-2021-00012)
  • (2019-2.1.7-ERANET-2020-00014)
The prevention of pre-eclampsia is difficult due to the syndromic nature and multiple underlying mechanisms of this severe complication of pregnancy. The current clinical distinction between early- and late-onset disease, although clinically useful, does not reflect the true nature and complexity of the pathologic processes leading to pre-eclampsia. The current gaps in knowledge on the heterogeneous molecular pathways of this syndrome and the lack of adequate, specific diagnostic methods are major obstacles to early screening and tailored preventive strategies. The development of novel diagnostic tools for detecting the activation of the identified disease pathways would enable early, accurate screening and personalized preventive therapies. We implemented a holistic approach that includes the utilization of different proteomic profiling methods of maternal plasma samples collected from various ethnic populations and the application of systems biology analysis to plasma proteomic, maternal demographic, clinical characteristic, and placental histopathologic data. This approach enabled the identification of four molecular subclasses of pre-eclampsia in which distinct and shared disease mechanisms are activated. The current review summarizes the results and conclusions from these studies and the research and clinical implications of our findings.
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2026-06-08 19:38