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Mid-trimester maternal plasma cytokines and CRP as predictors of spontaneous preterm birth
Authors:Michael S. Kramer  Susan R. Kahn  Robert W. Platt  Jacques Genest  Moy Fong Chen  Lise Goulet  Louise Séguin  John Lydon  Helen McNamara  Michael Libman  Mourad Dahhou  Julie Lamoureux  Kristin Skogstrand  Poul Thorsen
Affiliation:1. Department of Environmental Health Sciences, University of Michigan School of Public Health, Ann Arbor, MI, USA;2. Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA;3. Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA
Abstract:
Most previous studies of maternal cytokines and preterm birth have analyzed immunologic biomarkers after the onset of labor or membrane rupture; fewer have examined the systemic (blood) immune response prior to labor onset. We carried out a case–control study nested in a large (n = 5337) prospective, multi-center cohort. Cohort women had an interview, examination, and venipuncture at 24–26 weeks. Frozen plasma samples in women with spontaneous preterm birth (n = 207) and approximately 2 term controls per case (n = 444) were analyzed using Luminex multianalyte profiling technology. Fresh placentas were fixed, stained, and blindly assessed for histologic evidence of infection/inflammation, decidual vasculopathy, and infarction, and vaginal swabs were analyzed for bacterial vaginosis and fetal fibronectin concentration. High maternal matrix metalloproteinase-9 (MMP-9) concentration, but none of the other cytokines or C-reactive protein (CRP), was significantly associated with spontaneous preterm birth [adjusted OR = 1.7 (1.1–2.4)] and showed a dose–response relation across quartiles. No association was observed, however, between maternal MMP-9 and placental infection/inflammation, bacterial vaginosis, or vaginal fetal fibronectin concentration. Our results require confirmation in future studies but suggest that a systemic immune response implicating MMP-9 may have an etiologic role in spontaneous preterm birth.
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