Abstract
Background
Dysregulation of inflammatory processes is linked to perinatal complications yet a comprehensive description of cytokine levels throughout the perinatal period is lacking. We report prospective, serial levels of 29 unique cytokines measured in maternal blood during pregnancy, in the cord blood at birth, and in the neonatal blood.
Methods
Pregnant women (n = 140) for recruited from a Midwest tertiary medical center. Blood was obtained at five timepoints: 12–20 weeks, 24–28 weeks, and at labor in the women, umbilical cord at birth, 24–72 h in the newborn. Cytokine levels were analyzed using an electrochemiluminescence-based immunoassay.
Results
Levels for 29 cytokines were measured. The data were separated into two groups: pregnancies with (n = 82) and without major complications (n = 53) (preterm birth, preeclampsia, diabetes mellitus). Eighteen cytokines showed significant changes over time (p < .002). The majority of the cytokines were highest in the newborn. No differences in cytokine levels between complication groups were noted at any timepoint.
Conclusions
This is the first known study to report prospective, serial cytokine levels throughout the perinatal period for pregnancies with/without complications. No differences in maternal cytokine levels between those with/without complications were detected; studies with a larger sample size would be needed to validate our current findings. Results also suggest cytokine dysregulation may be more localized to the placenta making it difficult to measure and predict during pregnancy using maternal systemic blood specimens.
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Acknowledgments
The authors wish to thank the staff and patients at Nebraska Medicine and Olson Center, Jocelyn Jones, Colton T. Roessner, and Ellen Steffensmeier.
Disclosure statements
The authors report no conflict of interest. The research reported in this publication was supported by the National Institute of Nursing at the National Institutes of Health under award number [K01NR014474] and a University of Nebraska Medical Center’s Edna Ittner Pediatric Support grant. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.