Optics and Imaging Centre, Doris Duke Medical Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Department of Obstetrics and Gynaecology and Women's Health and HIV Research Group, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Curr Hypertens Rep. 2020 Mar 21;22(5):35. doi: 10.1007/s11906-020-01040-6.
To provide insight on the imbalance of angiogenic and lymphangiogenic factors in pre-eclampsia, as well as highlight polymorphism in genes related to angiogenesis and lymphangiogenesis.
The pregnancy-specific disorder pre-eclampsia is diagnosed by the presence of hypertension with/without proteinuria, after 20 weeks of gestation. The pathogenesis of pre-eclampsia remains ambiguous, but research over the years has identified an imbalance in maternal and foetal factors. Familial predisposition and gene variation are also linked to pre-eclampsia development. The sFlt-1/PIGF ratio has attracted great attention over the years; more recently several researchers have reported that a sFlt-1/PIGF ratio of ≤ 38 can be used to predict short-term absence of pre-eclampsia. This ratio has the potential to prevent adverse pregnancy outcomes and reduce healthcare costs significantly. Genome-wide studies have additionally identified variation in the foetal gene near Flt-1. The development of preeclampsia is not limited to the maternal interface, but foetal involvement as well as genetic interplay is associated with the disorder.
探讨子痫前期中血管生成和淋巴管生成因子失衡的原因,并重点介绍与血管生成和淋巴管生成相关基因的多态性。
子痫前期是一种妊娠特有的疾病,其诊断标准为妊娠 20 周后出现高血压伴/不伴蛋白尿。子痫前期的发病机制仍不明确,但多年来的研究已经确定了母体和胎儿因素的失衡。家族易感性和基因突变也与子痫前期的发生有关。可溶性血管内皮生长因子受体 1(sFlt-1)/胎盘生长因子(PIGF)比值多年来一直备受关注;最近有研究人员报道,sFlt-1/PIGF 比值≤38 可用于预测短期内是否会发生子痫前期。该比值有可能显著降低不良妊娠结局的发生率并降低医疗成本。全基因组研究还发现了 Flt-1 附近胎儿基因的变异。子痫前期的发生不仅局限于母体界面,胎儿的参与以及遗传相互作用也与该疾病有关。