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白藜芦醇补充口服硝苯地平治疗妊娠高血压综合征的疗效。

Efficacy of resveratrol to supplement oral nifedipine treatment in pregnancy-induced preeclampsia.

作者信息

Ding Jian, Kang Yan, Fan Yuqin, Chen Qi

机构信息

Department of Obstetrics and GynecologyMaternal and Child Health Care Hospital of Shandong Province, Jinan, Shandong Province, China.

Department of Obstetrics and GynecologyProvincial Hospital Affiliated to Shandong University, Jinan, Shandong Province, China.

出版信息

Endocr Connect. 2017 Nov;6(8):595-600. doi: 10.1530/EC-17-0130.

Abstract

OBJECTIVE

Preeclampsia (PE) is a complication affecting pregnant women worldwide, which usually manifests as severe maternal hypertension. Resveratrol (RESV), a naturally existing polyphenol, is known to exhibit beneficial effects in cardiovascular disease including hypertension. We evaluated the outcome of treatment combining oral nifedipine (NIFE) and RESV against PE.

DESIGN AND METHODS

Using a randomized group assignment, 400 PE patients were enrolled and received oral treatments of either NIFE + RESV or NIFE + placebo. Primary endpoints were defined as time to control blood pressure and time before a new hypertensive crisis. Secondary endpoints were defined as the number of doses needed to control blood pressure, maternal and neonatal adverse effects.

RESULTS

Compared with the NIFE + placebo group, the time needed to control blood pressure was significantly reduced in NIFE + RESV group, while time before a new hypertensive crisis was greatly delayed in NIFE + RESV group. The number of treatment doses needed to control blood pressure was also categorically lower in NIFE + RESV group. No differences in maternal or neonatal adverse effects were observed between the two treatment groups.

CONCLUSION

Our data support the potential of RESV as a safe and effective adjuvant of oral NIFE to attenuate hypertensive symptoms among PE patients.

摘要

目的

子痫前期(PE)是一种影响全球孕妇的并发症,通常表现为严重的母体高血压。白藜芦醇(RESV)是一种天然存在的多酚,已知在包括高血压在内的心血管疾病中具有有益作用。我们评估了口服硝苯地平(NIFE)联合RESV治疗PE的效果。

设计与方法

采用随机分组,纳入400例PE患者,接受NIFE + RESV或NIFE + 安慰剂的口服治疗。主要终点定义为控制血压的时间和新的高血压危机前的时间。次要终点定义为控制血压所需的剂量数、母体和新生儿不良反应。

结果

与NIFE + 安慰剂组相比,NIFE + RESV组控制血压所需时间显著缩短,而新的高血压危机前的时间在NIFE + RESV组显著延迟。NIFE + RESV组控制血压所需的治疗剂量数也明显较少。两个治疗组在母体或新生儿不良反应方面未观察到差异。

结论

我们的数据支持RESV作为口服NIFE的安全有效佐剂,以减轻PE患者高血压症状的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf02/5633060/e441a8a15204/ec-6-595-g001.jpg

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