首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Elevated blood pressure in offspring born premature to hypertensive pregnancy: is endothelial dysfunction the underlying vascular mechanism?
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Elevated blood pressure in offspring born premature to hypertensive pregnancy: is endothelial dysfunction the underlying vascular mechanism?

机译:高血压妊娠过早出生的后代血压升高:内皮功能障碍是潜在的血管机制吗?

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Offspring born to mothers with hypertensive pregnancy have higher childhood blood pressure. We hypothesized this relates to prenatally programmed differences in the underlying vascular pathophysiology of the offspring and that these would be most apparent in those born preterm because of severe hypertension. We carried out a 20-year follow-up study of 71 subjects born preterm, 19 to a hypertensive pregnancy and 52 to a normotensive pregnancy. Findings were compared with 38 subjects born at term to uncomplicated pregnancies. Peripheral and central blood pressures were measured, and then central arterial stiffness was assessed by carotid-femoral pulse wave velocity using applanation tonometry. Ultrasound was used to assess flow-mediated endothelial-dependent and independent brachial artery responses and common carotid artery intima-media thickness. Offspring born preterm to either hypertensive or normotensive pregnancy had higher peripheral and central blood pressure compared with full-term born offspring (central mean arterial pressure after preterm hypertensive pregnancy: 84.92+/-7.0 mm Hg; preterm normotensive pregnancy: 84.13+/-8.9 mm Hg; full-term pregnancy: 76.24+/-7.96 mm Hg; P=0.0009). However, underlying vascular phenotype differed. Preterm offspring of normotensive pregnancy had greater arterial stiffness than offspring of hypertensive pregnancy (5.92+/-0.84 versus 5.42+/-0.73 m/s; P=0.039), whereas offspring of hypertensive pregnancy had greater carotid intima-media thickness (0.52+/-0.04 versus 0.48+/-0.06 mm; P=0.013) and 30% lower flow-mediated dilatation (4.25+/-4.02% versus 6.79+/-4.38%; P=0.05). Prematurity is associated with elevated blood pressure in later life. However, predominant underlying vascular phenotype depends on maternal pathology. Targeting endothelial function may be particularly important for primary prevention after hypertension in pregnancy.
机译:患有高血压妊娠的母亲所生的后代的儿童血压较高。我们假设这与后代的潜在血管病理生理学的产前程序性差异有关,并且在严重高血压的早产儿中,这些差异最明显。我们对71名早产儿,19名高血压妊娠和52名血压正常妊娠的受试者进行了为期20年的随访研究。将研究结果与足月出生的38例无并发症妊娠的受试者进行了比较。测量外周和中央血压,然后使用压平眼压计通过颈股股脉搏波速度评估中央动脉僵硬度。超声用于评估血流介导的内皮依赖性和非依赖性肱动脉反应以及颈总动脉内膜-中膜厚度。与足月出生的孩子相比,早产或高血压怀孕的子孙的外周和中心血压更高(早产高血压怀孕后的中心平均动脉压:84.92 +/- 7.0 mm Hg;早血压的怀孕:84.13 +/- 8.9毫米汞柱;足月妊娠:76.24 +/- 7.96毫米汞柱; P = 0.0009)。但是,潜在的血管表型不同。血压正常妊娠的早产儿的动脉僵硬度比高血压妊娠的早产儿(5.92 +/- 0.84比5.42 +/- 0.73 m / s; P = 0.039)大,而高血压妊娠的后代的颈动脉内膜中层厚度更大(0.52+ /-0.04对0.48 +/- 0.06毫米; P = 0.013)和30%较低的流介导扩张(4.25 +/- 4.02%对6.79 +/- 4.38%; P = 0.05)。早产与以后的血压升高有关。但是,主要的基础血管表型取决于母体病理。靶向内皮功能对于妊娠高血压后的一级预防尤其重要。

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