Villar J, Purwar M, Merialdi M, Zavaleta N, Thi Nhu Ngoc N, Anthony J, De Greeff A, Poston L, Shennan A
Nuffield Department of Obstetrics and Gynaecology, Oxford Maternal and Perinatal Health Institute, Green Templeton College, University of Oxford, Oxford, UK.
BJOG. 2009 May;116(6):780-8. doi: 10.1111/j.1471-0528.2009.02158.x.
To determine if vitamin C and E supplementation in high-risk pregnant women with low nutritional status reduces pre-eclampsia.
Multicentred, randomised, controlled, double-blinded trial.
Antenatal care clinics and Hospitals in four countries.
Pregnant women between 14 and 22 weeks' gestation.
Randomised women received 1000 mg vitamin C and 400 iu of vitamin E or placebo daily until delivery.
Pre-eclampsia, low birthweight, small for gestational age and perinatal death.
Six hundred and eighty-seven women were randomised to the vitamin group and 678 to the placebo group. Groups had similar gestational ages (18.1; SD 2.4 weeks), socio-economic, clinical and demographical characteristics and blood pressure at trial entry. Risk factors for eligibility were similar, except for multiple pregnancies: placebo group (14.7%), vitamins group (11.8%). Previous pre-eclampsia, or its complications, was the most common risk factor at entry (vitamins 41.6%, placebo 41.3%). Treatment compliance was 87% in the two groups and loss to follow-up was low (vitamins 2.0%, placebo 1.3%). Supplementation was not associated with a reduction of pre-eclampsia (RR: 1.0; 95% CI: 0.9-1.3), eclampsia (RR: 1.5; 95% CI: 0.3-8.9), gestational hypertension (RR: 1.2; 95% CI: 0.9-1.7), nor any other maternal outcome. Low birthweight (RR: 0.9; 95% CI: 0.8-1.1), small for gestational age (RR: 0.9; 95% CI: 0.8-1.1) and perinatal deaths (RR: 0.8; 95% CI: 0.6-1.2) were also unaffected.
Vitamins C and E at the doses used did not prevent pre-eclampsia in these high-risk women.
确定营养状况不佳的高危孕妇补充维生素C和E是否能降低先兆子痫的发生率。
多中心、随机、对照、双盲试验。
四个国家的产前护理诊所和医院。
妊娠14至22周的孕妇。
随机分组的孕妇每天接受1000毫克维生素C和400国际单位维生素E或安慰剂,直至分娩。
先兆子痫、低出生体重、小于胎龄儿和围产期死亡。
687名妇女被随机分配到维生素组,678名被分配到安慰剂组。两组的孕周相似(18.1;标准差2.4周),入组时的社会经济、临床和人口统计学特征以及血压相似。除多胎妊娠外,入选的危险因素相似:安慰剂组(14.7%),维生素组(11.8%)。既往先兆子痫或其并发症是入组时最常见的危险因素(维生素组41.6%,安慰剂组41.3%)。两组的治疗依从率为87%,失访率较低(维生素组2.0%,安慰剂组1.3%)。补充维生素与先兆子痫(相对危险度:1.0;95%可信区间:0.9 - 1.3)、子痫(相对危险度:1.5;95%可信区间:0.3 - 8.9)、妊娠高血压(相对危险度:1.2;95%可信区间:0.9 - 1.7)的降低无关,也与任何其他母亲结局无关。低出生体重(相对危险度:0.9;95%可信区间:0.8 - 1.1)、小于胎龄儿(相对危险度:0.9;95%可信区间:0.8 - 1.1)和围产期死亡(相对危险度:0.8;95%可信区间:0.6 - 1.2)也未受影响。
所用剂量的维生素C和E不能预防这些高危妇女发生先兆子痫。