Hofmeyr G Justus, Manyame Sarah
Walter Sisulu University, University of the Witwatersrand, Eastern Cape Department of Health, East London, South Africa.
Cochrane Database Syst Rev. 2017 Sep 26;9(9):CD011192. doi: 10.1002/14651858.CD011192.pub2.
Pre-eclampsia is considerably more prevalent in low- than high-income countries. One possible explanation for this discrepancy is dietary differences, particularly calcium deficiency. Calcium supplementation in the second half of pregnancy reduces the serious consequences of pre-eclampsia and is recommended by the World Health Organization (WHO) for women with low dietary calcium intake, but has limited effect on the overall risk of pre-eclampsia. It is important to establish whether calcium supplementation before and in early pregnancy has added benefit. Such evidence would be justification for population-level fortification of staple foods with calcium.
To determine the effect of calcium supplementation or food fortification with calcium, commenced before or early in pregnancy and continued at least until mid-pregnancy, on pre-eclampsia and other hypertensive disorders, maternal morbidity and mortality, as well as fetal and neonatal outcomes.
We searched the Cochrane Pregnancy and Childbirth Trials Register (10 August 2017), PubMed (29 June 2017), ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (10 August 2017) and reference lists of retrieved studies.
Randomised controlled trials of calcium supplementation or food fortification which include women of child bearing age not yet pregnant, or in early pregnancy. Cluster-RCTs, quasi-RCTs and trials published in abstract form only would have been eligible for inclusion in this review but none were identified. Cross-over designs are not appropriate for this intervention.The scope of this review is to consider interventions including calcium supplementation with or without additional supplements or treatments, compared with placebo or no intervention.
Two review authors independently assessed trials for inclusion and risk of bias, extracted data and checked them for accuracy.
This review is based on one RCT (involving 60 women) which looked at calcium plus additional supplements versus control. The women (who had low antioxidant status) were in the early stages of pregnancy. We did not identify any studies where supplementation commenced pre-pregnancy. Another RCT comparing calcium versus placebo is ongoing but not yet complete. We did not identify any studies looking at any of our other planned comparisons. Calcium plus antioxidants and other supplements versus placeboWe included one small study (involving 60 women with low antioxidant levels) which was conducted in an academic hospital in Indondesia. The study was at low risk of bias for all domains with the exception of selective reporting, for which it was unclear. Women in the intervention group received calcium (800 mg) plus N-acetylcysteine (200 mg), Cu (2 mg), Zn (15 mg), Mn (0.5 mg) and selenium (100 mcg) and vitamins A (1000 IU), B6 (2.2 mg), B12 (2.2 mcg), C (200 mg), and E (400 IU) versus the placebo control group of women who received similar looking tablets containing iron and folic acid. Both groups received iron (30 mg) and folic acid (400 mcg). Tablets were taken twice daily from eight to 12 weeks of gestation and then throughout pregnancy.The included study found that calcium supplementation plus antioxidants and other supplements may slightly reduce pre-eclampsia (gestational hypertension and proteinuria) (risk ratio (RR) 0.24, 95% confidence interval (CI) 0.06 to 1.01; low-quality evidence), but this is uncertain due to wide confidence intervals just crossing the line of no effect, and small sample size. It appears that earlypregnancy loss before 20 weeks' gestation (RR 0.06, 95% CI 0.00 to 1.04; moderate-quality evidence) may be slightly reduced by calcium plus antioxidants and other supplements, but this outcome also has wide confidence intervals, which just cross the line of no effect. Very few events were reported under the composite outcome, severe maternal morbidity and mortality index and no clear difference was seen between groups (RR 0.36, 95% CI 0.04 to 3.23; low-quality evidence). However, the included study observed a reduction in the composite outcome pre-eclampsia and/or pregnancy loss at any gestational age (RR 0.13, 95% CI 0.03 to 0.50; moderate-quality evidence), and pregnancy loss/stillbirth at any gestational age (RR 0.06, 95% CI 0.00 to 0.92; moderate-quality evidence) in the calcium plus antioxidant/supplement group.Other outcomes reported (placental abruption, severe pre-eclampsia and preterm birth (less than 37 weeks' gestation)) were too infrequent for meaningful analysis. No data were reported for the outcomes caesarean section, birthweight < 2500 g, Apgar score less than seven at five minutes, death or admission to neonatal intensive care unit (ICU), or pregnancy loss, stillbirth or neonatal death before discharge from hospital.
AUTHORS' CONCLUSIONS: The results of this review are based on one small study in which the calcium intervention group also received antioxidants and other supplements. Therefore, we are uncertain whether any of the effects observed in the study were due to calcium supplementation or not. The evidence in this review was graded low to moderate due to imprecision. There is insufficient evidence on the effectiveness or otherwise of pre- or early-pregnancy calcium supplementation, or food fortification for preventing hypertensive disorders of pregnancy.Further research is needed to determine whether pre- or early-pregnancy supplementation, or food fortification with calcium is associated with a reduction in adverse pregnancy outcomes such as pre-eclampsia and pregnancy loss. Such studies should be adequately powered, limited to calcium supplementation, placebo-controlled, and include relevant outcomes such as those chosen for this review.There is one ongoing study of calcium supplementation alone versus placebo and this may provide additional evidence in future updates.
子痫前期在低收入国家比高收入国家更为普遍。这种差异的一个可能解释是饮食差异,尤其是钙缺乏。孕期后半期补充钙可降低子痫前期的严重后果,世界卫生组织(WHO)建议饮食钙摄入量低的女性补充钙,但对子痫前期的总体风险影响有限。确定孕前和孕早期补充钙是否有额外益处很重要。这样的证据可为在人群层面用钙强化主食提供依据。
确定在孕前或孕早期开始并至少持续至孕中期的补充钙或用钙强化食物对子痫前期和其他高血压疾病、孕产妇发病率和死亡率以及胎儿和新生儿结局的影响。
我们检索了Cochrane妊娠和分娩试验注册库(2017年8月10日)、PubMed(2017年6月29日)、ClinicalTrials.gov、WHO国际临床试验注册平台(ICTRP)(2017年8月10日)以及检索到的研究的参考文献列表。
补充钙或用钙强化食物的随机对照试验,纳入尚未怀孕或处于孕早期的育龄妇女。整群随机对照试验、半随机对照试验和仅以摘要形式发表的试验本应符合纳入本综述的条件,但未检索到。交叉设计不适用于此干预措施。本综述的范围是考虑包括补充钙(有或无其他补充剂或治疗)与安慰剂或不干预相比的干预措施。
两位综述作者独立评估试验是否纳入及偏倚风险,提取数据并检查其准确性。
本综述基于一项随机对照试验(涉及60名女性),该试验比较了钙加其他补充剂与对照组。这些女性(抗氧化状态低)处于孕早期。我们未找到任何孕前开始补充的研究。另一项比较钙与安慰剂的随机对照试验正在进行但尚未完成。我们未找到任何针对其他计划比较的研究。钙加抗氧化剂和其他补充剂与安慰剂相比
我们纳入了一项在印度尼西亚一家学术医院进行的小型研究(涉及60名抗氧化水平低的女性)。除选择性报告方面风险不明外,该研究在所有领域的偏倚风险均较低。干预组女性接受钙(800毫克)加N - 乙酰半胱氨酸(200毫克)、铜(2毫克)、锌(15毫克)、锰(0.5毫克)、硒(100微克)以及维生素A(1000国际单位)、B6(2.2毫克)、B12(2.2微克)、C(200毫克)和E(4国际单位),而安慰剂对照组女性接受外观相似的含 铁和叶酸的片剂。两组均接受铁(30毫克)和叶酸(400微克)。片剂在妊娠8至12周期间每日服用两次,然后持续整个孕期。
纳入的研究发现,补充钙加抗氧化剂和其他补充剂可能会略微降低子痫前期(妊娠期高血压和蛋白尿)(风险比(RR)0.24,95%置信区间(CI)0.06至1.01;低质量证据),但由于置信区间较宽且刚好越过无效应线以及样本量小,这一点尚不确定。补充钙加抗氧化剂和其他补充剂似乎可能会略微降低妊娠20周前的早期妊娠丢失(RR 0.06,95%CI 0.00至1.04;中等质量证据),但该结果的置信区间也较宽,刚好越过无效应线。在综合结局严重孕产妇发病率和死亡率指数下报告的事件极少,两组之间未观察到明显差异(RR 0.36,95%CI 0.04至3.23;低质量证据)。然而,纳入的研究观察到补充钙加抗氧化剂/补充剂组在任何孕周的子痫前期和/或妊娠丢失的综合结局(RR 0.13,95%CI 0.03至0.50;中等质量证据)以及任何孕周的妊娠丢失/死产(RR 0.06,95%CI 0.00至0.92;中等质量证据)方面有所降低。
报告的其他结局(胎盘早剥、重度子痫前期和早产(妊娠少于37周))发生频率过低,无法进行有意义的分析。未报告剖宫产、出生体重<2500克、5分钟时阿氏评分低于7分、死亡或入住新生儿重症监护病房(ICU)以及出院前妊娠丢失、死产或新生儿死亡等结局的数据。
本综述的结果基于一项小型研究,其中钙干预组还接受了抗氧化剂和其他补充剂。因此,我们不确定该研究中观察到的任何效应是否归因于补充钙。由于不精确性,本综述中的证据质量等级为低到中等。关于孕前或孕早期补充钙或用钙强化食物预防妊娠高血压疾病的有效性,证据不足。
需要进一步研究以确定孕前或孕早期补充钙或用钙强化食物是否与降低子痫前期和妊娠丢失等不良妊娠结局相关。此类研究应有足够的样本量,限于补充钙,采用安慰剂对照,并包括如本综述所选的相关结局。有一项正在进行的单独比较补充钙与安慰剂的研究,这可能会在未来更新中提供更多证据。