Piacvezérelt kutatás-fejlesztési és innovációs projektek támogatása(2020-1.1.2-PIACI-KFI-2021-00273)
Támogató: 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.