Maternal zinc deficiency during pregnancy elevates the risks of fetal growth restriction: a population-based birth cohort study

Sci Rep. 2015 Jun 8:5:11262. doi: 10.1038/srep11262.

Abstract

We investigated the association between maternal zinc level during pregnancy and the risks of low birth weight (LBW) and small for gestational age (SGA) infants in a large population-based birth cohort study. In this study, 3187 pregnant women were recruited. For serum zinc level, 2940 pregnant women were sufficient (≥56 μg/dL) and 247 deficient (<56 μg/dL). Of interest, 7.3% newborns were with LBW among subjects with low zinc level (RR: 3.48; 95% CI: 2.03, 5.96; P < 0.001). Adjusted RR for LBW was 3.41 (95% CI: 1.97, 5.91; P < 0.001) among subjects with low zinc level. Moreover, 15.0% newborns were with SGA among subjects with low zinc level (RR: 1.98; 95% CI: 1.36, 2.88; P < 0.001). Adjusted RR for SGA was 1.93 (95% CI: 1.32, 2.82; P < 0.001) among subjects with low zinc level. A nested case-control study within above cohort showed that maternal serum zinc level was lower in SGA cases as compared with controls. By contrast, maternal serum C-reactive protein, TNF-α and IL-8 levels were significantly higher in SGA cases than that of controls. Moreover, nuclear NF-κB p65 was significantly up-regulated in placentas of SGA cases as compared with controls. Taken together, maternal zinc deficiency during pregnancy elevates the risks of LBW and SGA infants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • C-Reactive Protein / metabolism
  • Case-Control Studies
  • Cohort Studies
  • Female
  • Fetal Development
  • Fetal Growth Retardation / physiopathology*
  • Gestational Age
  • Humans
  • Infant, Newborn
  • Infant, Small for Gestational Age / physiology*
  • Interleukin-8 / blood
  • Maternal-Fetal Exchange
  • Placenta / metabolism*
  • Pregnancy
  • Transcription Factor RelA / biosynthesis
  • Tumor Necrosis Factor-alpha / blood
  • Up-Regulation
  • Zinc / blood*
  • Zinc / deficiency*

Substances

  • CXCL8 protein, human
  • Interleukin-8
  • RELA protein, human
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • C-Reactive Protein
  • Zinc