Winer Norbert, Misbert Emilie, Masson Damien, Girault Aude, Alexandre-Gouabau Marie-Cecile, Ducarme Guillaume, Dochez Vincent, Thubert Thibault, Boivin Marion, Ferchaud-Roucher Véronique, Péré Morgane, Darmaun Dominique
Department of Gynecology and Obstetrics, Centre Hospitalier Universitaire de Nantes, Nantes, France; Nantes Université, NUN, UMR 1280 PhAN INRAE, Nantes, France.
Department of Gynecology and Obstetrics, Centre Hospitalier Universitaire de Nantes, Nantes, France.
Am J Clin Nutr. 2025 Feb;121(2):488-496. doi: 10.1016/j.ajcnut.2024.12.001. Epub 2024 Dec 9.
Preeclampsia (PE) contributes to maternal and fetal mortality and morbidity. Supplementation with L-arginine, the precursor of nitric oxide, has not proven effective, possibly due to extensive arginine catabolism in the splanchnic bed. Citrulline is converted by the kidney to L-arginine. Citrulline, therefore, could be a more effective nitric oxide donor in the treatment of PE.
The study aimed to determine whether oral L-citrulline supplementation would prolong the delay between diagnosis and delivery in preeclamptic females.
A total of 115 females with monofetal preeclamptic pregnancy were enrolled before 36 weeks of gestation in a multicenter randomized, double-blind trial: 58 received oral L-citrulline supplementation, and 57 received placebo. The duration of pregnancy, neonatal and maternal outcomes, and soluble fms-like tyrosine kinase 1/placental growth factor ratio, an index of placental dysfunction, were monitored.
Gestational age at inclusion was similar in both groups. The duration of pregnancy between inclusion and delivery was unaltered (hazard ratio: 0.90; 95% confidence interval: 0.62, 1.31). Neither neonatal weight nor pregnancy outcome differed between groups. Liver enzymes were higher on the day of delivery in the treated, compared to the placebo group (65.1 compared with 33.2 UI and 70.4 compared with 33.7 UI for alanine aminotransferase and aspartate aminotransferase, respectively, (estimate: 5.92; 95% confidence interval: 1.09, 10.74). Systolic blood pressure (BP) was higher at delivery in the citrulline group compared with the control group (P = 0.015), whereas the diastolic BP showed no difference. We did not find any difference in neonatal outcomes nor soluble fms-like tyrosine kinase 1/placental growth factor ratio.
The current trial found no benefit of oral L-citrulline supplementation to females with PE regarding either the duration of pregnancy, fetal growth, or maternal and neonatal outcomes. Systolic BP and liver enzymes levels were found to increase at delivery in the treated group. L-citrulline oral supplementation does not seem to be a promising candidate as a therapeutic intervention in pregnancies with PE. This trial was registered at CITRUPE as NCT02801695.
子痫前期(PE)会导致母婴死亡和发病。补充一氧化氮的前体L-精氨酸尚未被证明有效,这可能是由于内脏床中精氨酸的广泛分解代谢所致。瓜氨酸可被肾脏转化为L-精氨酸。因此,瓜氨酸可能是治疗PE更有效的一氧化氮供体。
本研究旨在确定口服补充L-瓜氨酸是否能延长子痫前期女性从诊断到分娩的间隔时间。
在一项多中心随机双盲试验中,共纳入了115名单胎子痫前期妊娠女性,她们均在妊娠36周前入组:58名接受口服L-瓜氨酸补充,57名接受安慰剂。监测了妊娠持续时间、新生儿和母亲结局,以及胎盘功能障碍指标可溶性fms样酪氨酸激酶1/胎盘生长因子比值。
两组入组时的孕周相似。入组至分娩的妊娠持续时间未改变(风险比:0.90;95%置信区间:0.62,1.31)。两组间新生儿体重和妊娠结局均无差异。与安慰剂组相比,治疗组分娩当天的肝酶水平更高(丙氨酸氨基转移酶分别为65.1比33.2 U/L,天冬氨酸氨基转移酶分别为70.4比33.7 U/L,(估计值:5.92;95%置信区间:1.09,10.74)。与对照组相比,瓜氨酸组分娩时的收缩压更高(P = 0.015),而舒张压无差异。我们未发现新生儿结局或可溶性fms样酪氨酸激酶1/胎盘生长因子比值有任何差异。
目前的试验发现,对于患有PE的女性,口服补充L-瓜氨酸在妊娠持续时间、胎儿生长或母婴结局方面均无益处。发现治疗组分娩时收缩压和肝酶水平升高。口服补充L-瓜氨酸似乎不是PE妊娠治疗干预的有前景的候选药物。本试验在CITRUPE注册,注册号为NCT02801695。