4.5 Article

Inflammatory and immune marker trajectories from pregnancy to one-year post-birth

Journal

CYTOKINE
Volume 149, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.cyto.2021.155758

Keywords

Pregnancy; Postpartum Period; Inflammatory; Proteins; Parity; BMI

Funding

  1. NIH [R01 HD073491]
  2. Colorado Clinical & Translational Sciences Institute (CCTSI)
  3. NIH/NCRR Colorado CTSI [UL1 RR025780]

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This study describes the trajectories of inflammatory and immune markers from pregnancy to a year post-birth, and investigates their associations with sociodemographic, health, and pregnancy-related variables. The results show that each biomarker has distinct patterns of change over time. Parity, pre-pregnancy BMI, and child sex are associated with the patterns of inflammatory markers.
Background: Pregnancy is an immunomodulatory state, with reported systematic changes in inflammatory and immune activity by pregnancy stage. Published data are inconsistent as to how inflammatory and immune markers change and recover across pregnancy and the postpartum period, or the sociodemographic, health and pregnancy-related factors that could affect biomarker trajectories. The purpose of this study is to describe inflammatory and immune marker trajectories from pregnancy to a year post-birth, and to test associations with sociodemographic, health and pregnancy-related variables. Methods: A sample of 179 pregnant women were assessed three times during pregnancy (between 8 and 36 weeks gestation) and three times during the postpartum period (between 1 and 12 months). Maternal sociodemographic characteristics, health, and pregnancy factors were obtained at study entry. Blood samples from each assessment were assayed for interleukin(IL)-6, tumor necrosis factor(TNF)alpha, IL-8, IL-10, and interferon(IFN)gamma. Multilevel modelling was used to characterize biomarker trajectories and associations with sociodemographic and health variables. Results: Distinct trajectories over time emerged for each biomarker. Male pregnancies were associated with higher TNF alpha, IL-10, and IFN gamma; higher pre-pregnancy BMI was associated with higher IL-6 and IFN gamma. Nulliparity was associated with greater increases in IL-6 and TNF alpha. Conclusions: Patterns observed for inflammatory and immune markers from pregnancy to a year postpartum support the hypothesis that the maternal immune system changes systematically across pregnancy and through an extended postpartum period. Parity, pre-pregnancy BMI and child sex are associated with inflammatory marker patterns over time. These results contribute to our understanding of how immune system activity changes from pregnancy to the post-birth period, and the factors that could affect those changes.

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