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子痫前期高危女性孕前及孕早期补钙:一项多中心、双盲、随机、安慰剂对照试验

Prepregnancy and early pregnancy calcium supplementation among women at high risk of pre-eclampsia: a multicentre, double-blind, randomised, placebo-controlled trial.

作者信息

Hofmeyr G Justus, Betrán Ana Pilar, Singata-Madliki Mandisa, Cormick Gabriela, Munjanja Stephen P, Fawcus Susan, Mose Simpiwe, Hall David, Ciganda Alvaro, Seuc Armando H, Lawrie Theresa A, Bergel Eduardo, Roberts James M, von Dadelszen Peter, Belizán José M

机构信息

Effective Care Research Unit, Eastern Cape Department of Health, Universities of the Witwatersrand, Walter Sisulu, and Fort Hare, East London, South Africa.

HRP-UNDP-UNFPA-UNICEF-WHO-World Bank Special Programme of Research, Development and Research Training in Human Reproduction, Department of Reproductive Health and Research, WHO, Geneva, Switzerland.

出版信息

Lancet. 2019 Jan 26;393(10169):330-339. doi: 10.1016/S0140-6736(18)31818-X.

Abstract

BACKGROUND

Reducing deaths from hypertensive disorders of pregnancy is a global priority. Low dietary calcium might account for the high prevalence of pre-eclampsia and eclampsia in low-income countries. Calcium supplementation in the second half of pregnancy is known to reduce the serious consequences of pre-eclampsia; however, the effect of calcium supplementation during placentation is not known. We aimed to test the hypothesis that calcium supplementation before and in early pregnancy (up to 20 weeks' gestation) prevents the development of pre-eclampsia METHODS: We did a multicountry, parallel arm, double-blind, randomised, placebo-controlled trial in South Africa, Zimbabwe, and Argentina. Participants with previous pre-eclampsia and eclampsia received 500 mg calcium or placebo daily from enrolment prepregnancy until 20 weeks' gestation. Participants were parous women whose most recent pregnancy had been complicated by pre-eclampsia or eclampsia and who were intending to become pregnant. All participants received unblinded calcium 1·5 g daily after 20 weeks' gestation. The allocation sequence (1:1 ratio) used computer-generated random numbers in balanced blocks of variable size. The primary outcome was pre-eclampsia, defined as gestational hypertension and proteinuria. The trial is registered with the Pan-African Clinical Trials Registry, number PACTR201105000267371. The trial closed on Oct 31, 2017.

FINDINGS

Between July 12, 2011, and Sept 8, 2016, we randomly allocated 1355 women to receive calcium or placebo; 331 of 678 participants in the calcium group versus 320 of 677 in the placebo group became pregnant, and 298 of 678 versus 283 of 677 had pregnancies beyond 20 weeks' gestation. Pre-eclampsia occurred in 69 (23%) of 296 participants in the calcium group versus 82 (29%) of 283 participants in the placebo group with pregnancies beyond 20 weeks' gestation (risk ratio [RR] 0·80, 95% CI 0·61-1·06; p=0·121). For participants with compliance of more than 80% from the last visit before pregnancy to 20 weeks' gestation, the pre-eclampsia risk was 30 (21%) of 144 versus 47 (32%) of 149 (RR 0·66, CI 0·44-0·98; p=0·037). There were no serious adverse effects of calcium reported.

INTERPRETATION

Calcium supplementation that commenced before pregnancy until 20 weeks' gestation, compared with placebo, did not show a significant reduction in recurrent pre-eclampsia. As the trial was powered to detect a large effect size, we cannot rule out a small to moderate effect of this intervention.

FUNDING

The University of British Columbia, a grantee of the Bill & Melinda Gates Foundation; UNDP-UNFPA-UNICEF-WHO-World Bank Special Programme of Research, Development and Research Training in Human Reproduction, WHO; the Argentina Fund for Horizontal Cooperation of the Argentinean Ministry of Foreign Affairs; and the Centre for Intervention Science in Maternal and Child Health.

摘要

背景

降低妊娠高血压疾病导致的死亡是全球优先事项。低膳食钙可能是低收入国家子痫前期和子痫高发病率的原因。已知妊娠后半期补充钙可降低子痫前期的严重后果;然而,胎盘形成期补充钙的效果尚不清楚。我们旨在检验妊娠前及妊娠早期(至妊娠20周)补充钙可预防子痫前期发生这一假设。

方法

我们在南非、津巴布韦和阿根廷进行了一项多中心、平行组、双盲、随机、安慰剂对照试验。有子痫前期和子痫病史的参与者从入组(孕前)至妊娠20周每天接受500毫克钙或安慰剂。参与者为经产妇,其最近一次妊娠合并子痫前期或子痫,且打算再次怀孕。所有参与者在妊娠20周后每天接受非盲法的1.5克钙。分配序列(1:1比例)使用计算机生成的随机数,按大小不等的平衡区组排列。主要结局是子痫前期,定义为妊娠高血压和蛋白尿。该试验已在泛非临床试验注册中心注册,注册号为PACTR201105000267371。试验于2017年10月31日结束。

结果

2011年7月12日至2016年9月8日期间,我们随机分配1355名女性接受钙或安慰剂治疗;钙组678名参与者中有331名怀孕,安慰剂组677名参与者中有320名怀孕,钙组678名中有298名、安慰剂组677名中有283名妊娠超过20周。妊娠超过20周的参与者中,钙组296名中有69名(23%)发生子痫前期,安慰剂组283名中有82名(29%)发生子痫前期(风险比[RR]0.80,95%置信区间0.61 - 1.06;p = 0.121)。对于从孕前最后一次访视至妊娠20周依从性超过80%的参与者,子痫前期风险在钙组144名中有30名(21%),安慰剂组149名中有47名(32%)(RR 0.66,置信区间0.44 - 0.98;p = 0.037)。未报告钙有严重不良反应。

解读

与安慰剂相比,妊娠前至妊娠20周开始补充钙并未显著降低复发性子痫前期的发生率。由于该试验有能力检测到较大的效应量,我们不能排除这种干预有小到中度的效果。

资助

英属哥伦比亚大学,比尔及梅琳达·盖茨基金会受赠方;联合国开发计划署 - 联合国人口基金 - 联合国儿童基金会 - 世界卫生组织 - 世界银行人类生殖研究、发展和研究培训特别规划,世界卫生组织;阿根廷外交部阿根廷横向合作基金;以及母婴健康干预科学中心。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abc/6346082/695879dc49d8/gr1.jpg

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