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Circulating angiogenic factors are related to the severity of gestational hypertension and preeclampsia, and their adverse outcomes

医学 子痫前期 胎盘生长因子 妊娠期 不利影响 妊娠高血压 内科学 可溶性fms样酪氨酸激酶-1 怀孕 胎龄 小于胎龄 胃肠病学 产科 血管内皮生长因子 血管内皮生长因子受体 生物 遗传学
作者
Alfredo Leaños‐Miranda,Francisco Méndez-Aguilar,Karla Leticia Ramírez-Valenzuela,Marilyn Serrano-Rodríguez,Guadalupe Berumen-Lechuga,Carlos José Molina-Pérez,Irma Isordia‐Salas,Inova Campos-Galicia
出处
期刊:Medicine [Wolters Kluwer]
卷期号:96 (4): e6005-e6005 被引量:37
标识
DOI:10.1097/md.0000000000006005
摘要

Gestational hypertension (GH) and preeclampsia (PE) are characterized by an imbalance in angiogenic factors. However, the relationship among these factors with the severity of hypertensive disorders of pregnancy (HDP) and adverse outcomes are not fully elucidated. We examined whether these biomarkers are related with the severity of HDP and adverse outcomes. Using a cross-sectional design, serum concentrations of placental growth factor (PlGF), soluble fms-like tyrosine kinase-1 (sFlt-1), and soluble endoglin were determined in 764 pregnant women: 75 healthy pregnant, 83 with mild GH (mGH), 105 with severe GH (sGH), 122 with mild PE (mPE), and 379 with severe PE (sPE). All angiogenic factors’ concentrations were significantly different (P ≤ 0.041) in HDP than in healthy pregnancy. In addition, these factors were markedly different in sPE than in mPE, sGH, or mGH (P ≤ 0.027) and in patients with sGH that in those with mPE or mGH (P < 0.05). As compared to mGH and mPE, patients with sGH and sPE had higher rates of both preterm delivery at <34 weeks of gestation and small-for-gestational age infants. Moreover, patients with sPE had higher rates of adverse maternal outcomes (P < 0.001) when compared to patients with mGH, sGH, or mPE. In all cases, levels of sFlt-1/PlGF ratio were significantly higher in patients with sGH and sPE who had adverse perinatal and maternal outcomes than in those with sGH and sPE who did not (P ≤ 0.016). Circulating concentrations of angiogenic factors appear to be suitable markers to assess the severity of GH and PE, and adverse outcomes.
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