Pre-Eclampsia: From Etiology and Molecular Mechanisms to Clinical Tools—A Review of the Literature

Pre-eclampsia is a severe pregnancy-related complication that manifests as a syndrome with multisystem involvement and damage. It has significantly grown in frequency during the past 30 years and could be considered as one of the major causes of maternal and fetal morbidity and mortality. However, t...

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Published inCurrent Issues in Molecular Biology Vol. 45; no. 8; pp. 6202 - 6215
Main Authors Tabacco, Sara, Ambrosii, Silvia, Polsinelli, Valentina, Fantasia, Ilaria, D’Alfonso, Angela, Ludovisi, Manuela, Cecconi, Sandra, Guido, Maurizio
Format Journal Article
LanguageEnglish
Published MDPI AG 25.07.2023
MDPI
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ISSN1467-3045
1467-3037
1467-3045
DOI10.3390/cimb45080391

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Summary:Pre-eclampsia is a severe pregnancy-related complication that manifests as a syndrome with multisystem involvement and damage. It has significantly grown in frequency during the past 30 years and could be considered as one of the major causes of maternal and fetal morbidity and mortality. However, the specific etiology and molecular mechanisms of pre-eclampsia are still poorly known and could have a variety of causes, such as altered angiogenesis, inflammations, maternal infections, obesity, metabolic disorders, gestational diabetes, and autoimmune diseases. Perhaps the most promising area under investigation is the imbalance of maternal angiogenic factors and its effects on vascular function, though studies in placental oxidative stress and maternal immune response have demonstrated intriguing findings. However, to determine the relative importance of each cause and the impact of actions aiming to significantly reduce the incidence of this illness, more research is needed. Moreover, it is necessary to better understand the etiologies of each subtype of pre-eclampsia as well as the pathophysiology of other major obstetrical syndromes to identify a clinical tool able to recognize patients at risk of pre-eclampsia early.
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ISSN:1467-3045
1467-3037
1467-3045
DOI:10.3390/cimb45080391