2017
DOI: 10.1038/ng.3895
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Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

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Cited by 211 publications
(172 citation statements)
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“…It is well established, however, that the condition is heterogeneous, with multiple pathways leading to vasoconstriction and end‐organ ischemia. Preeclampsia aggregates in families,6 and new evidence suggests that fetal genetic variants near FLT1 (fms‐related tyrosine kinase 1), a gene involved in angiogenesis, may contribute to risk 7, 8. Precise causes of preeclampsia are still unknown, but contributors are impaired angiogenesis,9 systemic endothelial dysfunction,10 and decreased vascular compliance resulting in impaired accommodation of the volume expansion required for healthy gestation 11.…”
Section: Pathophysiology and Risk Factorsmentioning
confidence: 99%
“…It is well established, however, that the condition is heterogeneous, with multiple pathways leading to vasoconstriction and end‐organ ischemia. Preeclampsia aggregates in families,6 and new evidence suggests that fetal genetic variants near FLT1 (fms‐related tyrosine kinase 1), a gene involved in angiogenesis, may contribute to risk 7, 8. Precise causes of preeclampsia are still unknown, but contributors are impaired angiogenesis,9 systemic endothelial dysfunction,10 and decreased vascular compliance resulting in impaired accommodation of the volume expansion required for healthy gestation 11.…”
Section: Pathophysiology and Risk Factorsmentioning
confidence: 99%
“…Moreover, the largest and most comprehensive genome‐wide association study also implicated a locus near fetal/placental FLT1 region in the development of preeclampsia, supporting the hypothesis that a placental isoform of sFlt1 is involved in the pathophysiology of the disease (McGinnis et al . ).…”
Section: Cardiorenal Syndromesmentioning
confidence: 97%
“…Des études familiales ont également permis de relier des régions génomiques au risque de PE, avec l'identification de gènes comme STOX1 (storkhead box 1) 1 , ou TNFSF13B (TNF superfamily member 13b) 2 . La première étude d'association GWAS (genome-wide association study) concernant la PE a été publiée très récemment [13]. Cette analyse, réalisée sur 4 380 cas et 310 238 témoins, a révélé un variant significatif (rs4769613) localisé à proximité du gène FLT1, confirmant ainsi l'impact de ce gène, codant en particulier sFLT1, dans la pathologie.…”
Section: Bases Immunologiques De La Prééclampsieunclassified