AI Article Synopsis

  • Eclampsia is one of the earliest documented diseases, with significant developments in understanding Pre-eclampsia over the years.
  • Major milestones include: the 1840 observation of proteinuria related to eclampsia by Rayer, and the 1897 identification of gestational hypertension by Vaquez.
  • In the late 20th century, research established that early and late-onset preeclampsia differ fundamentally, influenced by factors such as trophoblast implantation issues or pre-existing maternal health conditions, particularly prevalent in developed countries.
  • Endothelial cell disease was recognized as a key characteristic of preeclampsia, sparking discussions on potential common factors like inositol phospho glycans that may link both

Article Abstract

Eclampsia (together with epilepsy) being the first disease ever written down since the beginning of writings in mankind 5000 years ago, we will make a brief presentation of the different major steps in comprehension of Pre-eclampsia. 1) 1840. Rayer, description of proteinuria in eclampsia, 2) 1897 Vaquez, discovery of gestational hypertension in eclamptic women, 3) In the 1970's, description of the "double" trophoblastic invasion existing only in humans (Brosens & Pijnenborg,), 4) between the 1970's and the 1990's, description of preeclampsia being a couple disease. The "paternity problem" (and therefore irruption of immunology), 5) at the end of the 1980's, a major step forward: Preeclampsia being a global endothelial cell disease (glomeruloendotheliosis, hepatic or cerebral endotheliosis, HELLP, eclampsia), inflammation (J.Roberts.C Redman, R Taylor), 6) End of the 1990's: Consensus for a distinction between early onset preeclampsia EOP and late onset LOP (34 weeks gestation), EOP being rather a problem of implantation of the trophoblast (and the placenta), LOP being rather a pre-existing maternal problem (obesity, diabetes, coagulopathies etc…). LOP is predominant everywhere on this planet, but enormously predominant in developed countries: 90% of cases. This feature is very different in countries where women have their first child very young (88% of world births), where the fatal EOP (early onset) occurs in more than 30% of cases. 7) What could be the common factor which could explain the maternal global endotheliosis in EOP and LOP? Discussion about the inositol phospho glycans P type.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817979PMC
http://dx.doi.org/10.1016/j.jri.2017.09.006DOI Listing

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