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Published on: February 7, 2018
Associations between oxidative stress biomarkers during pregnancy and infant cognition at 7.5 months
Stephanie M Eick1, Kaegan Ortlund2, Andréa Aguiar3,4
1Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Insights
Oxidative stress in pregnancy may impact infant cognitive development. Higher levels of certain oxidative stress biomarkers were linked to reduced novelty preference, suggesting poorer recognition memory in infants.
Area of Science:
- Neuroscience
- Developmental Biology
- Environmental Health
Background:
- Oxidative stress is implicated in neurodevelopmental delay.
- Research on oxidative stress and infant cognitive outcomes is limited.
- Infancy is a critical period for brain development.
Purpose of the Study:
- To investigate the association between maternal urinary oxidative stress biomarkers and infant cognitive function.
- To assess effects on information processing speed, recognition memory, and attention.
Main Methods:
- Analysis of a subset (N=144) from the Illinois Kids Development Study.
- Measurement of four urinary oxidative stress biomarkers (8-isoprostane-PGF2α, 2,3-dinor-5,6-dihydro-8-iso-PGF2α, 2,3-dinor-8-iso-PGF2α, prostaglandin-F2α) from second and third trimesters.
- Infant cognition assessed using a visual recognition memory task measuring novelty preference, run duration, time to familiarization, and shift rate.
Main Results:
- Elevated levels of 8-isoprostane-PGF2α, 2,3-dinor-8-iso-PGF2α, and prostaglandin-F2α were associated with decreased novelty preference.
- These biomarkers were also linked to a modest increase in shift rate.
- Findings suggest a potential link between maternal oxidative stress and infant recognition memory.
Conclusions:
- Maternal exposure to oxidative stress during pregnancy may negatively affect infant cognitive development, particularly recognition memory.
- Further research is warranted to confirm these associations and explore underlying mechanisms.
- Early life oxidative stress could be a modifiable factor influencing neurodevelopmental trajectories.
Abstract:
Oxidative stress has been identified as an important biological pathway leading to neurodevelopmental delay. However, studies assessing the effects of oxidative stress on cognitive outcomes during infancy, a critical period of neurodevelopment, are limited. Our analysis included a subset of those enrolled in the Illinois Kids Development Study (N = 144). Four oxidative stress biomarkers (8-isoprostane-PGF2α , 2,3-dinor-5,6-dihydro-8-iso-PGF2α , 2,3-dinor-8-iso-PGF2α , and prostaglandin-F2α ) were measured in second and third trimesters urine and were averaged. Infant cognition was measured using a visual recognition memory task consisting of five blocks, each with one familiarization trial (two identical stimuli) and two test trials (one familiar and one novel stimulus). Outcomes measured included average run duration (a measure of information processing speed), novelty preference (a measure of recognition memory), time to reach familiarization, and shift rate (measures of attention). Linear regression was used to estimate associations between individual oxidative stress biomarkers and each outcome. Increasing 8-isoprostane-PGF2α , 2,3-dinor-8-iso-PGF2α , and prostaglandin-F2α were associated with a decrease in novelty preference (β = -0.02, 95% confidence interval [CI] = -0.03, 0.00; β = -0.02, 95% CI = -0.04, 0.00; β = -0.01, 95% CI = -0.02, 0.00, respectively), as well as a modest increase in shift rate. These findings suggest that oxidative stress may be associated with poorer recognition memory in early infancy.
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