Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2024 Nov;154(11):3400-3406.
doi: 10.1016/j.tjnut.2024.08.032. Epub 2024 Sep 13.

Effects of Vitamin D-3 Supplementation During Pregnancy and Lactation on Maternal and Infant Biomarkers of Environmental Enteric Dysfunction, Systemic Inflammation, and Growth: A Secondary Analysis of a Randomized Controlled Trial

Affiliations
Randomized Controlled Trial

Effects of Vitamin D-3 Supplementation During Pregnancy and Lactation on Maternal and Infant Biomarkers of Environmental Enteric Dysfunction, Systemic Inflammation, and Growth: A Secondary Analysis of a Randomized Controlled Trial

Jacqueline M Lauer et al. J Nutr. 2024 Nov.

Abstract

Background: Environmental enteric dysfunction (EED) is an acquired, subclinical state of intestinal inflammation common in children and adults in low-income and middle-income countries. Although vitamin D-3 supplementation has purported anti-inflammatory properties, its ability to ameliorate biomarkers of EED remains unclear.

Objectives: This study aimed to examine the effects of maternal vitamin D-3 supplementation during pregnancy and lactation on biomarkers of EED, systemic inflammation, and growth in women living with HIV and their infants in Dar es Salaam, Tanzania.

Methods: We conducted subgroup analyses among randomly selected mothers (n = 720) and infants (n = 365 at 6 wk of age, and n = 266 at 6 mo of age) who participated in a randomized, triple-blind, placebo-controlled trial of daily maternal 3000 IU vitamin D-3 supplementation from the second trimester of pregnancy until 1 y postpartum. Biomarkers of EED (soluble CD14 and intestinal fatty acid-binding protein), systemic inflammation (C-reactive protein and α1-acid glycoprotein), and growth factors (insulin-like growth factor 1 and fibroblast growth factor 21) were measured via the Micronutrient and Environmental Enteric Dysfunction Assessment Tool. Anti-flagellin and anti-lipopolysaccharide immunoglobulins were measured via enzyme-linked immunosorbent assay. Comparisons by randomized treatment arm were performed using ordinary least squares regression models with log2-transformed biomarkers.

Results: At 32 wk of gestation, intestinal fatty acid-binding protein (β: -0.19; P = 0.03) and α1-acid glycoprotein (β:-0.11; P = 0.04) were significantly lower in mothers in the vitamin D-3 group than those in mothers in the placebo group. At 6 wk of age, insulin-like growth factor 1 (β:-0.31; P = 0.03) was significantly lower in infants whose mothers were in the vitamin D-3 group than that in infants whose mothers were in the placebo group.

Conclusions: Vitamin D-3 supplementation during pregnancy and lactation reduced selected EED and systemic inflammation biomarkers among women living with HIV. While the effects of maternal vitamin D-3 supplementation do not appear to extend to infants, there may be an effect on growth factors. This trial was registered at clinicaltrials.gov as NCT02305927 (https://clinicaltrials.gov/study/NCT02305927).

Keywords: HIV; biomarkers; environmental enteric dysfunction; growth hormone resistance; infants; inflammation; pregnancy; supplementation; vitamin D.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest CPD reports financial support was provided by National Institute of Diabetes and Digestive and Kidney Diseases. CRS reports financial support was provided by National Institute of Child Health and Human Development. The other authors report no conflict of interest.

Figures

FIGURE 1
FIGURE 1
Flow diagram of the study. EED, environmental enteric dysfunction; Ig, immunoglobulin; LPS, lipopolysaccharide; MEEDAT, Micronutrient and Environmental Enteric Dysfunction Assessment Tool.

References

    1. Prendergast A., Kelly P. Enteropathies in the developing world: neglected effects on global health. Am. J. Trop. Med. Hyg. 2012;86:756–763. - PMC - PubMed
    1. Kosek M., Haque R., Lima A., Babji S., Shrestha S., Qureshi S., et al. Fecal markers of intestinal inflammation and permeability associated with the subsequent acquisition of linear growth deficits in infants. Am. J. Trop. Med. Hyg. 2013;88:390–396. - PMC - PubMed
    1. Keusch G.T., Denno D.M., Black R.E., Duggan C., Guerrant R.L., Lavery J.V., et al. Environmental enteric dysfunction: pathogenesis, diagnosis, and clinical consequences. Clin. Infect. Dis. 2014;59:S207–S212. - PMC - PubMed
    1. Korpe P.S., Petri W.A., Jr. Environmental enteropathy: critical implications of a poorly understood condition. Trends Mol. Med. 2012;18:328–336. - PMC - PubMed
    1. Syed S., Ali A., Duggan C. Environmental enteric dysfunction in children: a review. J. Pediatr. Gastroenterol. Nutr. 2016;63:6. - PMC - PubMed

Publication types

Associated data