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
. 2017 Jan 7;18(1):3.
doi: 10.1186/s12865-016-0184-6.

Oxidative stress biomarkers and their relationship with cytokine concentrations in overweight/obese pregnant women and their neonates

Affiliations

Oxidative stress biomarkers and their relationship with cytokine concentrations in overweight/obese pregnant women and their neonates

María Hernández-Trejo et al. BMC Immunol. .

Abstract

Background: Oxidative damage present in obese/overweight mothers may lead to further oxidative stress conditions or inflammation in maternal and cord blood samples. Thirty-four pregnant women/newborn pairs were included in this study to assess the presence of oxidative stress biomarkers and their relationship with serum cytokine concentrations. Oxidative stress biomarkers and antioxidant enzymes were compared between the mother/offspring pairs. The presence of 27 cytokines was measured in maternal and cord blood samples. Analyses were initially performed between all mothers and newborns and later between normal weight and mothers with overweight and obesity, and diabetic/non-diabetic women.

Results: Significant differences were found in biomarker concentrations between mothers and newborns. Additionally, superoxide-dismutase activity was higher in pre-pregnancy overweight mothers compared to those with normal weight. Activity for this enzyme was higher in neonates born from mothers with normal pregestational weight compared with their mothers. Nitrites in overweight/obese mothers were statistically lower than in their offspring. Maternal free fatty acids, nitrites, carbonylated proteins, malondialdehyde and superoxide dismutase predicted maternal serum concentrations of IL-4, IL-13, IP-10 and MIP-1β. Arginase activity in maternal plasma was related to decreased concentrations of IL-4 and IL-1β in cord arterial blood. Increased maternal malondialdehyde plasma was associated with higher levels of IL-6 and IL-7 in the offspring.

Conclusions: Oxidative stress biomarkers differ between mothers and offspring and can predict maternal and newborn cytokine concentrations, indicating a potential role for oxidative stress in foetal metabolic and immunologic programming. Moreover, maternal obesity and diabetes may affect maternal microenvironments, and oxidative stress related to these can have an impact on the placenta and foetal growth.

Keywords: Arginase; Cytokines; Diabetes; Free fatty acids; Nitrites; Obesity; Offspring; Oxidative stress; Pregnancy; Vitamin supplementation.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Analysis of variance. Mean differences in maternal age, kg gained during pregnancy, newborn’s gestational age, and newborn weight between overweight/obese mothers and normal-weight mothers
Fig. 2
Fig. 2
Oxidative stress biomarkers in mother/offspring pairs. Means and standard deviations (n = 34). Differences evaluated by paired-samples t Student test. SOD = Superoxide dismutase, GSH-Px = Glutathione peroxidase, MDA = malondialdehyde, LOOH = Lipid-hydroperoxides, FFA = Free fatty acid, CP = Carbonylated proteins. SOD, GSH-Px and ARG values reflect enzymatic activity in erythrocytes (nmol/mg of protein or U/mL)
Fig. 3
Fig. 3
Mean differences of oxidative stress biomarkers in the mother/offspring groups and in mothers vs. neonates, according to BMI, diabetes status, and the use of multivitamins and anti-inflammatory drugs. (n = 34 mother/offspring pairs). SOD = Superoxide dismutase (U/mL), CP = Carbonylated proteins (nmol DNPH/mg of protein), Nitrites (nmol/mg protein/min), Arg = Arginase activity (nmol/mg proteins/min), MDA = Malondialdehyde (nmol of carbocyanine/mg of dry weight), NDPH = dinitrophenylhydrazine. a Pre-pregnancy BMI. b BMI at the end of pregnancy. c Multi-vitamin consumption during pregnancy. d Use of anti-inflammatories during pregnancy. e Diabetes during pregnancy. f Hyperglycaemia during pregnancy

Similar articles

Cited by

References

    1. Catalano PM, Presley L, Minium J, Hauguel-de Mouzon S. Fetuses of obese mothers develop insulin resistance in utero. Diabetes Care. 2009;32(6):1076–1080. doi: 10.2337/dc08-2077. - DOI - PMC - PubMed
    1. Malti N, Merzouk H, Merzouk SA, Loukidi B, Karaouzene N, Malti A, Narce M. Oxidative stress and maternal obesity: Feto-placental unit interaction. Placenta. 2014;35(6):411–416. doi: 10.1016/j.placenta.2014.03.010. - DOI - PubMed
    1. Heslehurst N, Simpson H, Ells LJ, Rankin J, Wilkinson J, Lang R, Brown TJ, Summerbell CD. The impact of maternal bmi status on pregnancy outcomes with immediate short-term obstetric resource implications: A meta-analysis. Obes Rev. 2008;9(6):635–683. doi: 10.1111/j.1467-789X.2008.00511.x. - DOI - PubMed
    1. Drake AJ, Reynolds RM. Impact of maternal obesity on offspring obesity and cardiometabolic disease risk. Reproduction. 2010;140(3):387–398. doi: 10.1530/REP-10-0077. - DOI - PubMed
    1. Pantham P, Aye ILMH, Powell TL. Inflammation in maternal obesity and gestational diabetes mellitus. Placenta. 2015;36(7):709–715. doi: 10.1016/j.placenta.2015.04.006. - DOI - PMC - PubMed

Publication types