Hofmeyr G Justus, Lawrie Theresa A, Atallah Alvaro N, Duley Lelia, Torloni Maria R
Department of Obstetrics and Gynaecology, East London Hospital Complex, University of the Witwatersrand, University of Fort Hare, Eastern Cape Department of Health, Frere and Cecilia Makiwane Hospitals, Private Bag X 9047, East London, Eastern Cape, South Africa, 5200.
Cochrane Database Syst Rev. 2014 Jun 24(6):CD001059. doi: 10.1002/14651858.CD001059.pub4.
Pre-eclampsia and eclampsia are common causes of serious morbidity and death. Calcium supplementation may reduce the risk of pre-eclampsia, and may help to prevent preterm birth.
To assess the effects of calcium supplementation during pregnancy on hypertensive disorders of pregnancy and related maternal and child outcomes.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (28 March 2013) and contacted study authors for more data where possible. We updated the search in May 2014 and added the results to the 'Awaiting Classification' section of the review.
Randomised controlled trials (RCTs) comparing high-dose (at least 1 g daily of calcium) or low-dose calcium supplementation during pregnancy with placebo or no calcium.
We assessed eligibility and trial quality, extracted and double-entered data.
High-dose calcium supplementation (≥1 g/day)We included 14 studies in the review, however one study contributed no data. We included 13 high-quality studies in our meta-analyses (15,730 women). The average risk of high blood pressure (BP) was reduced with calcium supplementation compared with placebo (12 trials, 15,470 women: risk ratio (RR) 0.65, 95% confidence interval (CI) 0.53 to 0.81; I² = 74%). There was also a significant reduction in the risk of pre-eclampsia associated with calcium supplementation (13 trials, 15,730 women: RR 0.45, 95% CI 0.31 to 0.65; I² = 70%). The effect was greatest for women with low calcium diets (eight trials, 10,678 women: average RR 0.36, 95% CI 0.20 to 0.65; I² = 76%) and women at high risk of pre-eclampsia (five trials, 587 women: average RR 0.22, 95% CI 0.12 to 0.42; I² = 0%). These data should be interpreted with caution because of the possibility of small-study effect or publication bias.The composite outcome maternal death or serious morbidity was reduced (four trials, 9732 women; RR 0.80, 95% CI 0.65 to 0.97; I² = 0%). Maternal deaths were not significantly different (one trial of 8312 women: calcium group one death versus placebo group six deaths). There was an anomalous increase in the risk of HELLP (haemolysis, elevated liver enzymes and low platelets) syndrome (two trials, 12,901 women: RR 2.67, 95% CI 1.05 to 6.82; I² = 0%) in the calcium group, however, the absolute number of events was low (16 versus six).The average risk of preterm birth was reduced in the calcium group (11 trials, 15,275 women: RR 0.76, 95% CI 0.60 to 0.97; I² = 60%) and amongst women at high risk of developing pre-eclampsia (four trials, 568 women: average RR 0.45, 95% CI 0.24 to 0.83; I² = 60%), but no significant reduction in neonatal high care admission. There was no overall effect on the risk of stillbirth or infant death before discharge from hospital (11 trials 15,665 babies: RR 0.90, 95% CI 0.74 to 1.09; I² = 0%).One study showed a reduction in childhood systolic BP greater than 95th percentile among children exposed to calcium supplementation in utero (514 children: RR 0.59, 95% CI 0.39 to 0.91). In a subset of these children, dental caries at 12 years old was also reduced (195 children, RR 0.73, 95% CI 0.62 to 0.87). Low-dose calcium supplementation (< 1 g/day)We included 10 trials (2234 women) that evaluated low-dose supplementation with calcium alone (4) or in association with vitamin D (3), linoleic acid (2), or antioxidants (1). Most studies recruited women at high risk for pre-eclampsia, and were at high risk of bias, thus the results should be interpreted with caution. Supplementation with low doses of calcium significantly reduced the risk of pre-eclampsia (RR 0.38, 95% CI 0.28 to 0.52; I² = 0%). There was also a reduction in hypertension, low birthweight and neonatal intensive care unit admission.
AUTHORS' CONCLUSIONS: Calcium supplementation (≥ 1 g/day) is associated with a significant reduction in the risk of pre-eclampsia, particularly for women with low calcium diets. The treatment effect may be overestimated due to small-study effects or publication bias. It also reduces preterm birth and the occurrence of the composite outcome 'maternal death or serious morbidity'. We considered these benefits to outweigh the increased risk of HELLP syndrome, which was small in absolute numbers. The World Health Organization recommends calcium 1.5 g to 2 g daily for pregnant women with low dietary calcium intake.The limited evidence on low-dose calcium supplementation suggests a reduction in pre-eclampsia, but needs to be confirmed by larger, high-quality trials. Pending such results, in settings of low dietary calcium where high-dose supplementation is not feasible, the option of lower-dose supplements (500 to 600 mg/day) might be considered in preference to no supplementation.
先兆子痫和子痫是严重发病和死亡的常见原因。补充钙可能会降低先兆子痫的风险,并有助于预防早产。
评估孕期补充钙对妊娠高血压疾病及相关母婴结局的影响。
我们检索了Cochrane妊娠与分娩组试验注册库(2013年3月28日),并在可能的情况下联系研究作者获取更多数据。我们于2014年5月更新了检索,并将结果添加到综述的“等待分类”部分。
比较孕期高剂量(每日至少1克钙)或低剂量补钙与安慰剂或不补钙的随机对照试验(RCT)。
我们评估了纳入标准和试验质量,提取并双人录入数据。
高剂量补钙(≥1克/天)
本综述纳入了14项研究,但有1项研究未提供数据。我们在荟萃分析中纳入了13项高质量研究(15730名女性)。与安慰剂相比,补钙可降低高血压的平均风险(12项试验,15470名女性:风险比(RR)0.65,95%置信区间(CI)0.53至0.81;I² = 74%)。补钙还可显著降低先兆子痫的风险(13项试验,15730名女性:RR 0.45,95%CI 0.31至0.65;I² = 70%)。对于钙摄入量低的女性(8项试验,10678名女性:平均RR 0.36,95%CI 0.20至0.65;I² = 76%)和先兆子痫高危女性(5项试验,587名女性:平均RR 0.22,95%CI 0.12至0.42;I² = 0%),效果最为显著。由于可能存在小研究效应或发表偏倚,这些数据应谨慎解读。
孕产妇死亡或严重发病的复合结局有所降低(4项试验,9732名女性;RR 0.80,95%CI 0.65至0.97;I² = 0%)。孕产妇死亡无显著差异(1项试验,8312名女性:钙组1例死亡,安慰剂组6例死亡)。然而,钙组中HELLP(溶血、肝酶升高和血小板减少)综合征的风险异常增加(2项试验,12901名女性:RR 2.67,95%CI 1.05至6.82;I² = 0%),但事件的绝对数量较低(16例对6例)。
钙组早产的平均风险降低(11项试验,15275名女性:RR 0.76,95%CI 0.60至0.97;I² = 60%),在先兆子痫高危女性中也有所降低(4项试验,568名女性:平均RR 0.45,95%CI 0.24至0.83;I² = 60%),但新生儿重症监护病房入院率无显著降低。对死产或出院前婴儿死亡的风险没有总体影响(11项试验,15665名婴儿:RR 0.90,95%CI 0.74至1.09;I² = 0%)。
一项研究表明,宫内暴露于补钙的儿童中,收缩压高于第95百分位数的情况有所减少(514名儿童:RR 0.59,95%CI 0.39至0.91)。在这些儿童的一个亚组中,12岁时的龋齿也有所减少(195名儿童,RR 0.73,95%CI 0.62至0.87)。
低剂量补钙(<1克/天)
我们纳入了10项试验(2234名女性),这些试验评估了单独补钙(4项)或与维生素D(3项)、亚油酸(2项)或抗氧化剂(1项)联合使用的低剂量补钙情况。大多数研究招募的是先兆子痫高危女性,且存在较高的偏倚风险,因此结果应谨慎解读。低剂量补钙可显著降低先兆子痫的风险(RR 0.38,95%CI 0.28至0.52;I² = 0%)。高血压、低出生体重和新生儿重症监护病房入院率也有所降低。
补钙(≥1克/天)可显著降低先兆子痫的风险,尤其是对于钙摄入量低的女性。由于小研究效应或发表偏倚,治疗效果可能被高估。它还可降低早产以及“孕产妇死亡或严重发病”的复合结局的发生率。我们认为这些益处超过了HELLP综合征增加的风险,而HELLP综合征的绝对数量较少。世界卫生组织建议饮食中钙摄入量低的孕妇每日补钙1.5克至2克。
关于低剂量补钙的有限证据表明可降低先兆子痫的风险,但需要更大规模、高质量的试验加以证实。在获得此类结果之前,在饮食中钙含量低且无法进行高剂量补钙的情况下,可优先考虑低剂量补充剂(500至600毫克/天)而非不补充。