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DOI 10.1016/j.ajog.2006.01.068

Медицинская библиотека · American journal of obstetrics and gynecology · 2006

World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women.

Villar José, Abdel-Aleem Hany, Merialdi Mario, Mathai Matthews, Ali Mohamed M, Zavaleta Nelly, Purwar Manorama, Hofmeyr Justus, Nguyen Thi Nhu Ngoc, Campódonico Liana, Landoulsi Sihem, Carroli Guillermo, Lindheimer Marshall, World Health Organization Calcium Supplementation for the Prevention of Preeclampsia Trial Group

СтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

The purpose of this trial was to determine whether calcium supplementation of pregnant women with low calcium intake reduces preeclampsia and preterm delivery.

STUDY

DESIGN

Randomized placebo-controlled, double-blinded trial in nulliparous normotensive women from populations with dietary calcium < 600 mg/d. Women who were recruited before gestational week 20 received supplements (1.5 g calcium/d or placebo) throughout pregnancy. Primary outcomes were preeclampsia and preterm delivery; secondary outcomes focused on severe morbidity and maternal and neonatal mortality rates.

RESULTS

The groups comprised 8325 women who were assigned randomly. Both groups had similar gestational ages, demographic characteristics, and blood pressure levels at entry. Compliance were both 85% and follow-up losses (calcium, 3.4%; placebo, 3.7%). Calcium supplementation was associated with a non-statistically significant small reduction in preeclampsia (4.1% vs 4.5%) that was evident by 35 weeks of gestation (1.2% vs 2.8%; P = .04). Eclampsia (risk ratio, 0.68: 95% CI, 0.48-0.97) and severe gestational hypertension (risk ratio, 0.71; 95% CI, 0.61-0.82) were significantly lower in the calcium group. Overall, there was a reduction in the severe preeclamptic complications index (risk ratio, 0.76; 95% CI, 0.66-0.89; life-table analysis, log rank test; P = .04). The severe maternal morbidity and mortality index was also reduced in the supplementation group (risk ratio, 0.80; 95% CI, 0.70-0.91). Preterm delivery (the neonatal primary outcome) and early preterm delivery tended to be reduced among women who were < or = 20 years of age (risk ratio, 0.82; 95% CI, 0.67-1.01; risk ratio, 0.64; 95% CI, 0.42-0.98, respectively). The neonatal mortality rate was lower (risk ratio, 0.70; 95% CI, 0.56-0.88) in the calcium group.

CONCLUSION

A 1.5-g calcium/day supplement did not prevent preeclampsia but did reduce its severity, maternal morbidity, and neonatal mortality, albeit these were secondary outcomes.

Для цитирования: Villar José, Abdel-Aleem Hany, Merialdi Mario, Mathai Matthews, Ali Mohamed M, Zavaleta Nelly, Purwar Manorama, Hofmeyr Justus, Nguyen Thi Nhu Ngoc, Campódonico Liana, Landoulsi Sihem, Carroli Guillermo, Lindheimer Marshall, World Health Organization Calcium Supplementation for the Prevention of Preeclampsia Trial Group. World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women.. American journal of obstetrics and gynecology. 2006. DOI: 10.1016/j.ajog.2006.01.068.

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