» Articles » PMID: 28124024

Iron Supplementation Alters Heme and Heme Oxygenase 1 (HO-1) Levels In Pregnant Women in Ghana

Overview
Publisher Symbiosis Group
Date 2017 Jan 27
PMID 28124024
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Iron supplementation is recommended for pregnant women to meet their iron requirement for a healthy pregnancy. The benefits and risks of universal iron supplementation during pregnancy in malaria endemic countries are currently being debated. As part of a broader study that focused on the effect of heme/HO-1 on pregnancy outcomes in malaria in pregnancy, we determined the association between iron supplementation and free heme levels in blood of pregnant women with and without malaria in Ghana. We hypothesized that pregnant women with malaria who took iron supplements will have higher levels of Heme/HO-1 than those who did not take iron supplements.

Methods: A total of 337 women were recruited for this study. Blood samples were collected for malaria diagnosis and heme/HO-1 measurement. Quantification of heme was done using a heme colorimetric assay kit and HO-1 levels were performed using Enzyme-Linked Immunosorbent Assay (ELISA) on plasma samples.

Results: Malaria positive iron supplemented women, in their third trimester, had significantly higher median levels of heme 59.3(43.1 - 60.4) than non-malaria iron supplemented women 35.7(33.0 - 62.2), . Also, malaria positive iron supplemented women had significant higher median levels of HO-16.2(IQR 4.9 - 8.1) than pregnant women who did not take iron supplements 2.9 (IQR 2.1 - 3.8), .

Conclusion: Although iron supplementation may be highly beneficial and improve pregnancy outcomes for iron deficient or anemic mothers, it is also likely that iron supplementation for pregnant women who are not iron deficient may put this group of women at risk for adverse pregnancy outcomes. Findings from this study sheds light on the effect of iron supplementation on malaria derived heme in pregnancy, which may inform how iron supplementation is recommended for pregnant women who are not iron deficient.

Citing Articles

Inhibition of Heme Oxygenase-1 by Zinc Protoporphyrin IX Improves Adverse Pregnancy Outcomes in Malaria During Early Gestation.

Cariaco Y, Almeida M, Araujo E, Briceno M, Duran-Rodriguez A, Franco R Front Immunol. 2022; 13:879158.

PMID: 35619717 PMC: 9127164. DOI: 10.3389/fimmu.2022.879158.


A novel murine model of post-implantation malaria-induced preterm birth.

Andrew A, Cooper C, Moore J PLoS One. 2022; 17(3):e0256060.

PMID: 35312688 PMC: 8936457. DOI: 10.1371/journal.pone.0256060.


A novel murine model for assessing fetal and birth outcomes following transgestational maternal malaria infection.

Morffy Smith C, Russ B, Andrew A, Cooper C, Moore J Sci Rep. 2019; 9(1):19566.

PMID: 31862902 PMC: 6925284. DOI: 10.1038/s41598-019-55588-8.


Modelling heme-mediated brain injury associated with cerebral malaria in human brain cortical organoids.

Harbuzariu A, Pitts S, Cespedes J, Oxendine Harp K, Nti A, Shaw A Sci Rep. 2019; 9(1):19162.

PMID: 31844087 PMC: 6914785. DOI: 10.1038/s41598-019-55631-8.

References
1.
Greenwood B . Asymptomatic malaria infections--do they matter?. Parasitol Today. 1987; 3(7):206-14. DOI: 10.1016/0169-4758(87)90061-5. View

2.
Scholl P, Tripathi A, Sullivan D . Bioavailable iron and heme metabolism in Plasmodium falciparum. Curr Top Microbiol Immunol. 2005; 295:293-324. DOI: 10.1007/3-540-29088-5_12. View

3.
Levytska K, Kingdom J, Baczyk D, Drewlo S . Heme oxygenase-1 in placental development and pathology. Placenta. 2013; 34(4):291-8. DOI: 10.1016/j.placenta.2013.01.004. View

4.
Pamplona A, Ferreira A, Balla J, Jeney V, Balla G, Epiphanio S . Heme oxygenase-1 and carbon monoxide suppress the pathogenesis of experimental cerebral malaria. Nat Med. 2007; 13(6):703-10. DOI: 10.1038/nm1586. View

5.
Bhutta Z, Ahmed T, Black R, Cousens S, Dewey K, Giugliani E . What works? Interventions for maternal and child undernutrition and survival. Lancet. 2008; 371(9610):417-40. DOI: 10.1016/S0140-6736(07)61693-6. View