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Soluble urokinase plasminogen activator receptor in vaginally collected amniotic fluid predicting fetal inflammatory response syndrome: a prospective cohort study.
Gulbiniene, Violeta; Dumalakiene, Irena; Balciuniene, Greta; Pilypiene, Ingrida; Narkeviciute, Ieva; Novickij, Vitalij; Vysniauskis, Gintautas; Ramasauskaite, Diana.
Afiliação
  • Gulbiniene V; Faculty of Medicine, Vilnius University, Vilnius, Lithuania. violeta.gulbiniene@mf.vu.lt.
  • Dumalakiene I; Department of Immunology, State Research Institute Center of Innovative Medicine, Vilnius, Lithuania.
  • Balciuniene G; Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Pilypiene I; Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Narkeviciute I; Department of Immunology, State Research Institute Center of Innovative Medicine, Vilnius, Lithuania.
  • Novickij V; Department of Immunology, State Research Institute Center of Innovative Medicine, Vilnius, Lithuania.
  • Vysniauskis G; Department of Immunology, State Research Institute Center of Innovative Medicine, Vilnius, Lithuania.
  • Ramasauskaite D; Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
BMC Pregnancy Childbirth ; 24(1): 54, 2024 Jan 10.
Article em En | MEDLINE | ID: mdl-38200448
ABSTRACT

BACKGROUND:

Improving noninvasive antenatal diagnosis of fetal inflammatory response syndrome (FIRS) can assist in the evaluation of prenatal risk and reduce perinatal outcomes. This study aimed to determine whether soluble urokinase-type plasminogen activator receptor (suPAR) in vaginally collected amniotic fluid is significant in identifying FIRS after preterm premature rupture of membranes before 34 weeks of gestation.

METHODS:

This was a prospective cohort study of 114 pregnant women and their newborns after preterm premature rupture of membranes at 22-34+6 weeks of gestation. SuPAR was evaluated using an enzyme-linked immunosorbent assay in vaginally collected amniotic fluid. Patients were classified according to the presence or absence of FIRS. FIRS was defined by umbilical cord blood interleukin-6 level > 11 pg/mL or histological funisitis. The data were analyzed using the R package (R-4.0.5).

RESULTS:

SuPAR was detected in all amniotic fluid samples with a median of 26.23 ng/mL (interquartile range (IQR), 15.19-51.14). The median level of suPAR was higher in the FIRS group than in the non-FIRS group, 32.36 ng/mL (IQR, 17.27-84.16) vs. 20.46 ng/mL (IQR, 11.49-36.63) (P = 0.01), respectively. The presence of histological chorioamnionitis significantly increased the suPAR concentration in the FIRS group (P < 0.001). The areas under the curve for FIRS and FIRS with histological chorioamnionitis were 0.65 and 0.74, respectively, with an optimum cutoff value of 27.60 ng/mL. Controlling for gestational age, the cutoff of suPAR more than 27.60 ng/mL predicted threefold higher odds for FIRS and sixfold higher odds for FIRS with histologic chorioamnionitis.

CONCLUSION:

Soluble urokinase-type plasminogen activator receptor in vaginally obtained amniotic fluid may assist in evaluating prenatal risk of FIRS in patients after preterm premature rupture of membranes before 34 weeks of gestation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Corioamnionite / Síndrome de Resposta Inflamatória Sistêmica / Nascimento Prematuro / Doenças Fetais Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Corioamnionite / Síndrome de Resposta Inflamatória Sistêmica / Nascimento Prematuro / Doenças Fetais Idioma: En Ano de publicação: 2024 Tipo de documento: Article