Calcium supplementation during pregnancy may reduce preterm delivery in high-risk populations

Jose Villar, John T. Repke

Research output: Contribution to journalArticle

108 Scopus citations

Abstract

Results are presented of a randomized, double-blinded controlled clinical trial of calcium supplementation (2.0 gm of elemental calcium as calcium carbonate) and a placebo. All participants were 17 years of age or less and clinically healthy. Patients were enrolled by the twenty third week of gestation. The mean duration of calcium supplementation or placebo was approximately 14 weeks. Treatment consisted of 2.8 (±1.5) tablets per day in the placebo group (N = 95) and 3.0 (±1.4) tables per day in the calcium group (N = 94). Dietary calcium intake was similar in both groups at about 1200 mg/day. Thecalcium group had a lower incidence of preterm delivery (<37 weeks; 7.4% vs 21.1%; p = 0.007); spontaneous labor and preterm delivery (6.4% vs 17.9%; p = 0.01); and low birth weight (9.6% vs 21.1%; p = 0.03). This effect was also present after stratified analysis by level of treatment compliance, urinary tract infection, and chlamydial infection. Life-table analysis demonstrated an overall shift to a higher gestational age in the calcium group compared with the placebo group (log-rank test, p = 0.02). As suggested previously, the observed effect could be mediated by a reduction in uterine smooth muscle contractibility. If confirmed by future research, these results could represent an important preventive intervention for prematurity in high-risk populations.

Original languageEnglish (US)
Pages (from-to)1124-1131
Number of pages8
JournalAmerican journal of obstetrics and gynecology
Volume163
Issue number4 PART 1
DOIs
Publication statusPublished - Oct 1990

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All Science Journal Classification (ASJC) codes

  • Obstetrics and Gynecology

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