Value of cervicovaginal fluid cytokines in prediction of fetal inflammatory response syndrome in pregnancies complicated with preterm premature rupture of membranes (pPROM)

J Perinat Med. 2020 Mar 26;48(3):249-255. doi: 10.1515/jpm-2019-0280.

Abstract

Background Preterm premature rupture of membranes (pPROM) is associated with a high risk of prematurity and complications of fetal inflammatory response syndrome (FIRS). The aim of the study is to determine any correlations between the concentration of selected cytokines contained in the cervicovaginal secretion eluates and in the umbilical cord plasma in patients with pPROM and to find the noninvasive markers of FIRS in order to pinpoint the optimal time of the delivery. Methods The study included 80 patients with pPROM between the 24th and 34th week of gestation. The cervicovaginal fluid and umbilical cord blood were collected. Interleukin 6 (IL-6), interleukin 10 (IL-10), interleukin 19 (IL-19) and tumor necrosis factor-α (TNF-α) concentrations were measured in both materials. For the statistical analysis, SigmaStat3.5 software was used. Results There was no direct association in levels of IL-6, TNF-α, IL-10 and IL-19 between the cord blood and cervicovaginal secretions within the studied group. The cut-off point of IL-6 of 26.8 pg/mL in the vaginal fluid had high sensitivity and specificity in order to discriminate between newborns with and without FIRS (81.08%; 76.74%). Conclusion Further studies are needed on a larger group of participants to demonstrate that an elevated concentration of IL-6 above 26.8 pg/mL in the cervicovaginal secretion eluate is an indirect noninvasive marker of FIRS.

Keywords: fetal inflammatory response syndrome; funisitis; histologic chorioamnionitis; interleukin 19; interleukin 6; premature rupture of membranes; prematurity; preterm birth; tumor necrosis factor-α.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Cytokines / metabolism*
  • Female
  • Fetal Diseases / etiology
  • Fetal Diseases / metabolism*
  • Fetal Membranes, Premature Rupture / metabolism*
  • Humans
  • Pregnancy
  • Systemic Inflammatory Response Syndrome / etiology
  • Systemic Inflammatory Response Syndrome / metabolism*
  • Vaginal Smears
  • Young Adult

Substances

  • Cytokines