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Identifying a biological signature of prenatal maternal stress
James M. Keane, Ali S. Khashan, Fergus P. McCarthy, Louise C. Kenny, James M. Collins, Sarah O’Donovan, Jillian Brown, John F. Cryan, Timothy G. Dinan, Gerard Clarke, Siobhain M. O’Mahony
James M. Keane, Ali S. Khashan, Fergus P. McCarthy, Louise C. Kenny, James M. Collins, Sarah O’Donovan, Jillian Brown, John F. Cryan, Timothy G. Dinan, Gerard Clarke, Siobhain M. O’Mahony
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Research Article Inflammation Neuroscience

Identifying a biological signature of prenatal maternal stress

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Abstract

Psychological stress affects maternal gastrointestinal (GI) permeability, leading to low-grade inflammation, which can negatively affect fetal development. We investigated a panel of circulating markers as a biological signature of this stress exposure in pregnant women with and without the stress-related GI disorder irritable bowel syndrome (IBS). Markers of GI permeability and inflammation were measured in plasma from healthy and IBS cohorts of women at 15 and 20 weeks’ gestation. Biomarkers were evaluated with respect to their degree of association to levels of stress, anxiety, and depression as indicated by responses from the Perceived Stress Scale, State-Trait Anxiety Inventory, and Edinburgh Postnatal Depression Scale. High levels of stress were associated with elevations of soluble CD14, lipopolysaccharide binding protein (LBP), and tumor necrosis factor–α, while anxiety was associated with elevated concentrations of C-reactive protein (CRP) in otherwise healthy pregnancies. Prenatal depression was associated with higher levels of soluble CD14, LBP, and CRP in the healthy cohort. High levels of prenatal anxiety and depression were also associated with lower concentrations of tryptophan and kynurenine, respectively, in the IBS cohort. These markers may represent a core maternal biological signature of active prenatal stress, which can be used to inform intervention strategies via stress reduction techniques or other lifestyle approaches. Such interventions may need to be tailored to reflect underlying GI conditions, such as IBS.

Authors

James M. Keane, Ali S. Khashan, Fergus P. McCarthy, Louise C. Kenny, James M. Collins, Sarah O’Donovan, Jillian Brown, John F. Cryan, Timothy G. Dinan, Gerard Clarke, Siobhain M. O’Mahony

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Figure 3

Differences in EPDS scoring groups across gestational time points in the healthy cohort (N = 24/61/19 from low/moderate/high).

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Differences in EPDS scoring groups across gestational time points in the...
(A) Heatmap of normalized biomarker means across scoring groups and time points. Individual boxes are represented on a scale from red to blue. Darker red boxes represent markers whose concentrations were found to be greater than 1 standard deviation lower than the mean concentration across stress group and time point. Darker blue boxes represent markers whose concentrations were found to be greater than 1 standard deviation higher than the mean concentration across stress group and time point. Lower z scores are evident for LBP, sCD14, and TNF-α in the low-scoring group at 15 and 20 weeks and for IL-8 and SDF-1α in the high-scoring group at 20 weeks. Higher z scores are evident for IFABP and Trp/Kyn ratio in the high-scoring group at 15 weeks and for CRP in the high-scoring group at 15 and 20 weeks. Significant differences between EPDS-scoring groups are illustrated for (B) LBP, (C) sCD14, (D) CRP, (E) TNF-α, and (F) IL-8 (2-way ANOVA with Tukey’s HSD). *P < 0.05.

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