Plasma IGFBP‐1, Fas, kallistatin, and P‐selectin as predictive biomarkers of histologic chorioamnionitis and associated intra‐amniotic infection in women with preterm labor

• Published in: American journal of reproductive immunology (1989) Vol. 89; no. 1; pp. e13645 - n/a
• Main Authors: Lee, Kyong‐No, Cho, Iseop, Im, Eun Mi, Oh, Eunji, Park, Kyo Hoon
• Format: Journal Article
• Language: English
• Published: Denmark Wiley Subscription Services, Inc 01.01.2023
• Subjects: Amniocentesis; Amniotic Fluid; biomarker; Biomarkers; Chorioamnionitis; Chorioamnionitis - diagnosis; Enzyme-linked immunosorbent assay; Female; Fetal alcohol syndrome; Gestational age; Haptoglobin; histologic chorioamnionitis; Humans; Infant, Newborn; Matrix Metalloproteinase 2; microbial invasion of the amniotic cavity; multi‐biomarker panel; Obstetric Labor, Premature; Pentraxins; Plasma; Prediction models; Pregnancy; preterm labor; Retrospective Studies; preterm labor; multi-biomarker panel; microbial invasion of the amniotic cavity; histologic chorioamnionitis; biomarker; plasma
• ISSN: 1046-7408; 1600-0897
• DOI: 10.1111/aji.13645

Problem To determine whether altered levels of 13 plasma biomarkers, alone or in combination, could be independently associated with histologic chorioamnionitis (HCA) and microbial‐associated HCA (defined as the presence of HCA along with microbial invasion) in women with preterm labor (PTL). Methods of Study This was a retrospective cohort study involving 77 singleton pregnant women with PTL (23–34 gestational weeks) who delivered within 96 h of plasma and amniotic fluid (AF) sampling. DKK‐3, E‐selectin, Fas, haptoglobin, IGFBP‐1, kallistatin, MMP‐2, MMP‐8, pentraxin 3, progranulin, P‐selectin, SAA4, and TGFBI levels were assayed in plasma samples by ELISA. AF obtained via amniocentesis was used for microorganism identification. Results Multiple logistic regression analyses revealed significant associations between low plasma IGFBP‐1 levels and acute HCA, and between low plasma Fas and kallistatin levels, and elevated plasma P‐selectin levels and microbial‐associated HCA (all p < .05), after adjusting for gestational age. Using a stepwise regression procedure, a multi‐biomarker panel for microbial‐associated HCA was developed, which included plasma MMP‐2, kallistatin, and P‐selectin levels (area under the curve [AUC], .867). The AUC for this three‐marker panel was significantly or borderline significantly greater than that of any single variable included in the panel. However, a predictive model for acute HCA could not be developed because only one variable (MMP‐2) was selected. Conclusions These findings demonstrate that IGFBP‐1, Fas, kallistatin, and P‐selectin are associated with acute HCA and microbial‐associated HCA in women with PTL. Their combined use can significantly improve the diagnostic ability for the detection of microbial‐associated HCA.