Amniotic Fluid Infection in Preterm Pregnancies with Intact Membranes

Myntti, Tarja; Rahkonen, Leena; Nupponen, Irmeli; Pätäri-Sampo, Anu; Tikkanen, Minna; Sorsa, Timo; Juhila, Juuso; Andersson, Sture; Paavonen, Jorma; Stefanovic, Vedran

doi:https://doi.org/10.1155/2017/8167276

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Research Article | Open Access

Volume 2017 | Article ID 8167276 | https://doi.org/10.1155/2017/8167276

Amniotic Fluid Infection in Preterm Pregnancies with Intact Membranes

Tarja Myntti,¹Leena Rahkonen,¹Irmeli Nupponen,²Anu Pätäri-Sampo,³Minna Tikkanen,¹Timo Sorsa,^4,5Juuso Juhila,⁶Sture Andersson,²Jorma Paavonen,¹and Vedran Stefanovic¹

Academic Editor: Irene Rebelo

Received11 Aug 2016

Revised18 Dec 2016

Accepted26 Dec 2016

Published12 Jan 2017

Abstract

Introduction. Intra-amniotic infection (IAI) is a major cause of preterm labor and adverse neonatal outcome. We evaluated amniotic fluid (AF) proteolytic cascade forming biomarkers in relation to microbial invasion of the amniotic cavity (MIAC) and IAI in preterm pregnancies with intact membranes. Material and Methods. Amniocentesis was made to 73 women with singleton pregnancies; 27 with suspected IAI; and 46 controls. AF biomarkers were divided into three cascades: Cascade 1: matrix metalloproteinase-8 (MMP-8), MMP-9, myeloperoxidase (MPO), and interleukin-6; Cascade 2: neutrophil elastase (HNE), elafin, and MMP-9; Cascade 3: MMP-2, tissue inhibitor of matrix metalloproteinases-1 (TIMP-1), MMP-8/TIMP-1 molar ratio, and C-reactive protein (CRP). MMP-8 was measured by an immunoenzymometric assay and the others were measured by ELISA. Standard biochemical methods, molecular microbiology, and culture techniques were used. Results. MMP-8, MMP-9, MPO, elafin, and TIMP-1 concentrations were higher in IAI suspected cases compared to controls and also in IAI suspected cases with MIAC compared to those without MIAC when adjusted by gestational age at amniocentesis. All biomarkers except elafin and MMP-2 had the sensitivity of 100% with thresholds based on ROC-curve. Odd ratios of biomarkers for MIAC were 1.2-38 and 95% confidential intervals 1.0-353.6. Conclusions. Neutrophil based AF biomarkers were associated with IAI and MIAC.

1. Introduction

Intra-amniotic infection (IAI), defined as microbial invasion of the amniotic cavity (MIAC) with intra-amniotic inflammation, is common in women with preterm labor and exists with or without preterm prelabor rupture of membranes (PPROM) [1]. MIAC often leads to IAI [2]. However, intra-amniotic inflammation in the absence of MIAC also occurs [3]. Amniocentesis and amniotic fluid (AF) rapid biomarker testing may help in optimal timing of delivery.

Infection may induce the degranulation of interleukin- (IL-) 6 and matrix metalloproteinases (MMP), from polymorphonuclear neutrophils (PMNs) [4]. MMP-8 has been linked to MIAC [5–7], inflammation [8–10], histological chorioamnionitis (HCA) [11], and adverse neonatal outcome [12, 13]. Several AF biomarkers form proteolytic cascades. They are formed in inflammatory conditions after recruitment and activation of neutrophils, which release their subcellular granules, that is, degranulating tissue destructive enzymes (for example, MMP-8, MMP-9, and neutrophil elastase (HNE)). Those and other such enzymes can form cascades by activating each other. The process leads to degradation of extracellular matrix components and modulation of cytokines [4], which may lead in obstetrics to membrane rupture or ripening and softening of the cervix.

MPO is the activator of MMP-8 and MMP-9, while IL-6 can act as their inducer (Cascade 1). HNE is an activator of MMP-9, and elafin is an antiprotease of HNE [14]. Elafin is produced not only by neutrophils but also by epithelial cells [14]. Thus, HNE and MMP-9 form another PMN-derived proteolytic cascade (Cascade 2), to which elafin associates. The third cascade comprises MMP-2, tissue inhibitor of matrix metalloproteinases-1 (TIMP-1), MMP-8/TIMP-1 molar ratio, and C-reactive protein (CRP) (Cascade 3). MMP-2 and TIMP-1 are not produced by PMNs.

While many reports on AF biomarkers in PPROM pregnancies exist, such studies of MIAC and IAI in preterm pregnancies with presumed intact membranes are only few [3, 15, 16].

2. Materials and Methods

This prospective study was conducted at the Department of Obstetrics and Gynecology, University Hospital, Helsinki, Finland, between June 2013 and October 2015. The Institutional Review Board approved the study protocol (Ref. number 75/13/03/03/2013). A written informed consent was obtained from all patients.

2.1. Patients

The study population consisted of 73 women who underwent amniocentesis with singleton pregnancy and presumed intact membranes. Twenty-seven women had suspected IAI. Among those, the median gestational age at amniocentesis was 27⁺⁴ weeks, ranging from 22⁺⁰ to 31⁺⁴. IAI was suspected in the presence of preterm contractions with at least one of the following criteria: uterine tenderness, fetal tachycardia, infectious discharge from cervix, maternal plasma CRP > 10 mg/L, total blood white cell (WBC) count > 20 × 10⁹/L, or visible sludge at ultrasound examination. Forty-six pregnant women with no suspected IAI served as controls (Table 1). In the control group the indication for amniocentesis was mid-trimester chromosomal analysis in 24 cases (52%), evaluation of fetal lung maturity [ (11%)], or exclusion of fetal chronic hypoxia by erythropoietin measurement [ (37%)]. Among controls, the gestational age at amniocentesis was (median, range) 23⁺¹ weeks (from 17⁺⁰ to 37⁺⁵). In the control group, five (11%) developed preeclampsia, four (9%) had insulin treated gestational diabetes, and four (9%) pregnancies were complicated by fetal growth restriction (fetal growth below -2 SD). Fetal structural anomaly, proven or suspected fetal aneuploidy, and diabetes type I were not eligible.

Gestational age was based on the first trimester ultrasonography screening. Membranes were presumed intact in the absence of any clinical signs of membrane rupture.

2.2. Collection of Samples and Laboratory Procedures

Transabdominal amniocentesis was performed by our study group members. AF samples were retrieved. MIAC was defined as a positive AF culture or positive bacterial PCR by 16S rRNA gene sequencing. The result of bacterial culture was available in 23 (85%) cases and in none of the controls and the result of AF-PCR in all cases and controls. The microbial analyses have been described in detail previously [15].

AF specimens were divided into aliquots, frozen and stored at −20°C until the biomarkers were analysed (Medix Biochemica, Espoo, Finland). AF-MMP-8 quantitation was made with a solid-phase immunoenzymometric assay (MMP-8 IEMA, Medix Biochemica, Espoo, Finland) and it was analysed according to the manufacturer’s instructions. The absorbance measurement was done at 414 nm using a microplate reader (Multiskan, Thermo Fisher Scientific, Vantaa, Finland). Other biomarkers were analysed by using commercial enzyme-linked immunosorbent assay (ELISA): AF-elafin [Human Trappin-2 (elafin) ELISA kit, RayBiotech, Norcross, GA, USA], AF-HNE [polymorphonuclear (Human PMN Elastase) Sandwich ELISA kit, eBioscience, Vienna, Austria], AF-IL-6 [interleukin-6 (IL-6) ELISA kit, R&D Systems, Minneapolis, USA], AF-MPO [myeloperoxidase (MPO) ELISA kit, Immundiagnostik AG, Bensheim, Hesse, Germany], AF-MMP-2 [matrix metalloproteinase-2 (MMP-2) ELISA kit, R&D Systems, Minneapolis, USA], AF-MMP-9 [matrix metalloproteinase-9 (MMP-9) ELISA kit, R&D Systems, Minneapolis, USA], AF-CRP [human C-reactive protein (CRP) ELISA kit, R&D Systems, Minneapolis, USA], and AF-TIMP-1 [tissue inhibitor of metalloproteinases 1 (TIMP-1) ELISA kit, GE Healthcare, Buckinghamshire, UK]. The inter- and intra-assay coefficients of variation for elafin were <10% and <12%, respectively; for HNE < 5% and < 6%, respectively; for IL-6 < 5% and < 5%, respectively; for MPO < 3% and < 5%, respectively; for MMP-2 < 7% and < 13%, respectively; for MMP-8 < 6% and < 6%, respectively; for MMP-9 < 3% and < 8%, respectively; for CRP < 10% and < 10%, respectively; and for TIMP-1 < 12% and < 16%, respectively. The limit of detection for elafin was 0.005 ng/mL, for HNE 0.00198 ng/mL, for IL-6 0.0007 ng/mL, for MPO 0.294 ng/mL, for MMP-2 0.37 ng/mL, for MMP-8 0.4 ng/mL, for MMP-9 0.156 ng/mL, for CRP 0.010 ng/mL, and for TIMP-1 1.25 ng/mL. For AF-LD the intra-assay coefficient of variation (CV) was <2.3% and the limit of detection of the assay was 5 IU/L. For AF-Gluc the detection limit was 0.50 mmol/L. In the concentration levels less than 4 mmol/L the intra-assay CV was 4.7% and at concentration levels from 4.1 mmol/L to 42 mmol/L 1.9%.

Patients were managed according to our clinical practice guidelines. During the study period, only the results of AF-lactate dehydrogenase (LD), AF-glucose (Gluc), AF-PCR, and AF bacterial culture were available to obstetricians in charge. The methods of AF-LD and AF-Gluc testing have been described previously [15, 17]. If AF-LD was less than 419 IU/L and AF-Gluc was more than 0.7 mmol/L [15] in the absence of MIAC, pregnancy could continue and patients were followed up as outpatients.

MMP-8 belongs to proinflammatory neutrophil based cascade but represents also a known biomarker in this study. The cut-off value for AF-MMP-8 was 41.5 ng/mL, which has shown a sensitivity of 100%, specificity of 69%, PPV of 62%, and NPV of 100% for MIAC in a previous study [18] and was considered consistent with inflammation. IAI was determined as AF-MMP-8 > 41.5 ng/mL in the presence of MIAC.

2.3. Neonatal Outcome

Data on deliveries (spontaneous, induced, or caesarean section) and neonates were collected from the hospital records. The short-term outcome variables for neonates were birth weight, Apgar score at 1 min and 5 min of age, umbilical artery pH and base excess (BE), need for neonatal intensive care unit, need for a respirator, and the presence of clinical sepsis or blood culture positive sepsis. CRP and WBC levels were recorded.

The diagnosis of neonatal sepsis was set by a neonatologist. Neonatal sepsis was categorized into clinical sepsis and blood culture positive sepsis. Clinical sepsis was defined as blood culture negative infection with symptoms consistent with sepsis, abnormal blood values, and positive response to a minimum of 5-day antibiotic treatment. Abnormal blood values supporting clinical sepsis diagnosis included elevated CRP more than 20 mg/L, leukocytosis or leukopenia, increased neutrophil precursors, thrombocytopenia, and no signs of other infections. The symptoms of clinical sepsis were respiratory distress, apnoea, tachycardia, poor perfusion, low blood pressure, fever, hypoglycaemia, hyperglycaemia, irritability, feeding problems, lethargy, and convulsions. Sepsis was categorized as present or absent. All neonates with clinical or blood culture positive sepsis received antibiotics.

Other outcome measures for neonates were respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), necrotising enterocolitis (NEC), retinopathy of prematurity (ROP), intraventricular hemorrhage (IVH), periventricular leukomalacia (PVL), or death.

2.4. Statistical Analysis

All calculations were carried out using Microsoft Statistical Package for Social Sciences (SPSS Inc., Chicago, IL, USA) for Windows v22.0. Categorical variables were compared by the chi-square test or Fisher’s exact test if the number of cases was under five. Data with continuous variables did not follow a normal distribution and were compared by Mann–Whitney test. Amniotic fluid biomarkers were regressed on gestational age at sample collection and on gestational age at delivery, and adjusted values were computed using the residual as a dependent variable. The correlations of biomarker concentrations with MMP-8 were tested with Spearman bivariate correlation. The receiver operating characteristics (ROC) curve was constructed, area under the curve (AUC) was estimated, and the sensitivity and specificity were calculated. Two-tailed tests were used. A value less than 0.05 was considered significant.

3. Results

The selected characteristics of the study population are shown in Table 1. MIAC was found in 7 women (26%) with suspected IAI (cases) and in none of the controls. Candida species were detected in two cases; other microbes (six different) were detected in one case each. MIAC was polymicrobial in one case (14%).

3.1. AF Biomarkers

Cascade 1. As shown in Table 2, the median concentrations of all biomarkers were higher in IAI suspected cases than in controls. When adjusted by gestational age at amniocentesis, all biomarkers except AF-IL-6 were higher in IAI suspected cases than in controls (Table 2). Among IAI suspected cases, all biomarkers were associated with MIAC, also when adjusted by gestational age (Table 3). The accuracies and the most optimal cut-off values based on ROC-curve are shown in Table 4. Among Cascade 1 biomarkers, MMP-9 had the highest risk for MIAC, OR 4.5 (95% CI 1.3–15.3) (Table 4).

Cascade 2. The median concentration of HNE did not differ between cases and controls, but the median concentration of elafin and MMP-9 was higher in cases than in controls, also when adjusted by gestational age (Table 2). All biomarkers in Cascade 2 were associated with MIAC, also when adjusted by gestational age (Table 3). The accuracies and the most optimal cut-off values based on ROC-curve are shown in Table 4.

Cascade 3. The median concentrations of all biomarkers except AF-CRP were higher in cases than in controls (Table 2). When adjusted for gestational age only MMP-2 and TIMP-1 concentrations differed between cases and controls (Table 2). TIMP-1 and MMP-8/TIMP-1 molar ratio were associated with MIAC in IAI suspected cases. MMP-2 and CRP were not associated with MIAC, even when adjusted by gestational age (Table 3). The accuracies and the most optimal cut-off values based on ROC-curve are shown in Table 4.

Among IAI suspected cases, AF-HNE had the highest correlation with AF-MMP-8 ( = 0.749, ), while AF-MMP-2 had the lowest one ( = 0.401, ). Among controls AF-HNE had the highest correlation with AF-MMP-8 ( = 0.671, ). The correlations of biomarkers except MMP-8 with MMP-8 separately in IAI suspected cases and in controls are shown in Figures 1 and 2.

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In IAI cases (MMP-8 > 41.5 ng/mL with MIAC) AF-CRP correlated with MMP-8 ( = 0.501, ), MMP-9 ( = 0.493, ), MPO ( = 0.645, ), IL-6 ( = 0.473, ), and MMP-8/TIMP-1 molar ratio ( = 0.556, ).

All biomarkers included were associated with IAI () and all except MMP-2 () were associated with AF inflammation () (data not shown).

3.2. Neonatal Outcome

Of all IAI suspected cases, 11 neonates (41%) were born before 32 gestational weeks. Of these 11, six were born spontaneously within 7 days from amniocentesis (Table 5). Four of these were born after induction of labor due to suspected infection and one was born with caesarean section due to massive maternal hemorrhage. Nine neonates (33%) exhibited prematurity-related adverse neonatal outcome, all born ≤ 29⁺⁰ gestational weeks. Six (67%) of those had MIAC. Two neonates had early-onset neonatal sepsis.

Only one of the 16 neonates born after 32 gestational weeks was born from IAI-case where Ureaplasma was detected by AF-PCR. AF-LD and AF-Gluc were normal in this case suggesting colonization. AF-IL-6 concentration was 5.6 ng/mL and AF-MMP-8 concentration was 144 ng/mL, but these values were not available for the clinician. AF-MMP-9 (), MPO (), HNE (), and MMP-8/TIMP-1 molar ratio () were associated with blood culture positive neonatal sepsis when the data were adjusted by gestational age at delivery (data not shown).

4. Discussion

We demonstrated that, among IAI suspected cases, all AF biomarkers from Cascades 1 and 2 were associated with MIAC, which was documented in one-fourth of our IAI suspected cases despite presumed intact membranes. The association persisted even after adjusting by gestational age at amniocentesis. Furthermore, in IAI cases AF biomarkers produced by neutrophils were associated with general inflammatory biomarker CRP [19] in AF. Additionally, neutrophil based biomarkers were able to both discriminate cases from controls after adjusting by gestational age at amniocentesis and associate with MIAC.

The problem with biomarkers commonly used, that is, AF-Gluc and AF-LD, is the limited accuracy for MIAC [15, 20, 21]. AF-MMP-8 and AF-IL-6 have been demonstrated to provide better accuracy [22] but are not commonly used in clinical practice. Rapid AF biomarkers are needed for optimal timing of delivery in women with suspected IAI.

We studied several AF biomarkers which form inflammation related proteolytic cascades. One can identify increased levels of PMN-derived biomarkers in MIAC cases. IL-6 can induce PMN extravasation at the site of inflammation, often triggered by microorganisms or virulence factors associated [4], and also act as a degranulation inducer.

Proinflammatory neutrophil-derived AF biomarkers (Cascade 1) associated with general inflammatory biomarker CRP in IAI cases though suggesting that activated and degranulating neutrophils are the major source of MMP-8 and MMP-9, MPO (Cascade 1), and HNE (Cascade 2) in the AF affected by MIAC. AF neutrophils are of maternal origin [1] reflecting maternal host response to infection. Cascade 3 biomarkers did not detect this since these biomarkers, MMP-2 and TIMP-1, are not produced and released by neutrophils [4, 23]. Furthermore, HNE and MPO can proteolytically and oxidatively inactivate TIMP-1, respectively, thus reducing the antiproteolytic defensive shield in AF [4, 23]. Infection leading to imbalance of MMP-8 and TIMP-1 may be related to initiation of preterm delivery [24].

MMP-9, IL-6, HNE, and elafin have been linked to MIAC in previous studies [14, 25–28], whereas MMP-2 has been associated with MIAC in PPROM pregnancies only [25]. TIMP-1 in AF has been linked to MMP-9 [29] and to MIAC in pregnancies with intact membranes [30], but in this study MIAC was not determined with PCR, as it was in our study. Thus, we confirmed and expanded the previous findings in IAI suspected cases with presumed intact membranes.

Several reports of AF-CRP and preterm delivery exist [31, 32], but only few include AF-CRP in the diagnosis of IAI [33]. In the study of Dulay exact AF-CRP values were not written out, but AF-CRP values differed by MIAC [33]. In that study both pregnancies with and without PPROM were included. Although AF-CRP is of fetal origin [34], we found that AF-CRP was not useful in IAI diagnostics or in predicting adverse neonatal outcome in pregnancies with presumed intact membranes. MIAC and funisitis have been associated with umbilical cord CRP-value [35], but our study had no intention to analyze postnatal cord samples.

We found that infection and inflammation occurred mainly at low gestational weeks, as also reported by Combs et al. [16]. So far, no randomized trials exist about the impact of amniocentesis in the management of preterm labor and PPROM on neonatal outcome. However, recent observational studies [36–39] suggest that it could be beneficial. Combs et al. [16] reported that AF infection or inflammation is associated with neonatal morbidity. However, we could not repeat this with any of the biomarkers studied. Smaller sample size and different clinical setting may explain this discrepancy.

Although this study had a relatively small sample size, we were able to show significant differences in biomarker concentrations between cases and controls. Multicentre study design is needed for larger sample size. Small sample size made multivariate analyses or adjustment of neonatal outcomes by gestational age meaningless. Larger studies are necessary to determine biomarker cut-off values for clinical practice and to find out whether a biomarker panel would be better than any single biomarker. The results have not been adjusted for gestational diabetes and preeclampsia, which is a limitation since some controls did have those background diseases, which may have some immune contribution. However, in the clinical practice it is important to find a biomarker working in the whole population, not just in those without any background diseases. Another limitation is the lack of molecular biology techniques in the definition of neonatal sepsis and the lack of microbial culture analysis in controls in the assessment of MIAC.

To our knowledge, this is the first study reporting the association of inflammation related proteolytic biomarker cascades with IAI. In summary, our results highlight the association of PMN-derived biomarkers with MIAC and IAI in preterm pregnancies with intact membranes.

Competing Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The study was funded by Helsinki University Hospital Research Grant (TYH2013340), by the Finnish Funding Agency for Technology and Innovation Grants 3986/31/2013 and 4059/31/2013, and by the SalWe Research Program “Get it Done” no. 534/14.

References

C. J. Kim, R. Romero, P. Chaemsaithong, N. Chaiyasit, B. H. Yoon, and Y. M. Kim, “Acute chorioamnionitis and funisitis: definition, pathologic features, and clinical significance,” American Journal of Obstetrics and Gynecology, vol. 213, no. 4, pp. S29–S52, 2015.
View at: Publisher Site | Google Scholar
S. L. Hillier, S. S. Witkin, M. A. Krohn, D. H. Watts, N. B. Kiviat, and D. A. Eschenbach, “The relationship of amniotic fluid cytokines and preterm delivery, amniotic fluid infection, histologic chorioamnionitis, and chorioamnion infection,” Obstetrics and Gynecology, vol. 81, no. 6, pp. 941–948, 1993.
View at: Google Scholar
R. Romero, J. Miranda, T. Chaiworapongsa et al., “Prevalence and clinical significance of sterile intra-amniotic inflammation in patients with preterm labor and intact membranes,” American Journal of Reproductive Immunology, vol. 72, no. 5, pp. 458–474, 2014.
View at: Publisher Site | Google Scholar
H. Alfakry, E. Malle, C. N. Koyani, P. J. Pussinen, and T. Sorsa, “Neutrophil proteolytic activation cascades: a possible mechanistic link between chronic periodontitis and coronary heart disease,” Innate Immunity, vol. 22, no. 1, pp. 85–99, 2016.
View at: Publisher Site | Google Scholar
C. W. Park, B. H. Yoon, S. M. Kim, J. S. Park, and J. K. Jun, “The frequency and clinical significance of intra-amniotic inflammation defined as an elevated amniotic fluid matrix metalloproteinase-8 in patients with preterm labor and low amniotic fluid white blood cell counts,” Obstetrics & Gynecology Science, vol. 56, no. 3, pp. 167–175, 2013.
View at: Publisher Site | Google Scholar
K. J. Oh, S. E. Lee, H. Jung, G. Kim, R. Romero, and B. H. Yoon, “Detection of ureaplasmas by the polymerase chain reaction in the amniotic fluid of patients with cervical insufficiency,” Journal of Perinatal Medicine, vol. 38, no. 3, pp. 261–268, 2010.
View at: Publisher Site | Google Scholar
E. Maymon, R. Romero, P. Pacora et al., “Human neutrophil collagenase (matrix metalloproteinase 8) in parturition, premature rupture of the membranes, and intrauterine infection,” American Journal of Obstetrics and Gynecology, vol. 183, no. 1, pp. 94–99, 2000.
View at: Publisher Site | Google Scholar
J. K. Nien, B. H. Yoon, J. Espinoza et al., “A rapid MMP-8 bedside test for the detection of intra-amniotic inflammation identifies patients at risk for imminent preterm delivery,” American Journal of Obstetrics and Gynecology, vol. 195, no. 4, pp. 1025–1030, 2006.
View at: Publisher Site | Google Scholar
S. E. Lee, R. Romero, S. M. Lee, and B. H. Yoon, “Amniotic fluid volume in intra-amniotic inflammation with and without culture-proven amniotic fluid infection in preterm premature rupture of membranes,” Journal of Perinatal Medicine, vol. 38, no. 1, pp. 39–44, 2010.
View at: Publisher Site | Google Scholar
S. M. Kim, R. Romero, J. Lee et al., “About one-half of early spontaneous preterm deliveries can be identified by a rapid matrix metalloproteinase-8 (MMP-8) bedside test at the time of mid-trimester genetic amniocentesis,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 29, no. 15, pp. 2414–2421, 2016.
View at: Publisher Site | Google Scholar
S. M. Kim, R. Romero, J. W. Park, K. J. Oh, J. K. Jun, and B. H. Yoon, “The relationship between the intensity of intra-amniotic inflammation and the presence and severity of acute histologic chorioamnionitis in preterm gestation,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 28, no. 13, pp. 1500–1509, 2015.
View at: Publisher Site | Google Scholar
E. Maymon, R. Romero, T. Chaiworapongsa et al., “Amniotic fluid matrix metalloproteinase-8 in preterm labor with intact membranes,” American Journal of Obstetrics and Gynecology, vol. 185, no. 5, pp. 1149–1155, 2001.
View at: Publisher Site | Google Scholar
J. Lee, K. J. Oh, H. J. Yang, J. S. Park, R. Romero, and B. H. Yoon, “The importance of intra-amniotic inflammation in the subsequent development of atypical chronic lung disease,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 22, no. 10, pp. 917–923, 2009.
View at: Publisher Site | Google Scholar
A. E. King, R. W. Kelly, J.-M. Sallenave, A. D. Bocking, and J. R. G. Challis, “Innate immune defences in the human uterus during pregnancy,” Placenta, vol. 28, no. 11-12, pp. 1099–1106, 2007.
View at: Publisher Site | Google Scholar
T. Myntti, L. Rahkonen, M. Tikkanen, A. Pätäri-Sampo, J. Paavonen, and V. Stefanovic, “Amniotic fluid rapid biomarkers are associated with intra-amniotic infection in preterm pregnancies regardless of the membrane status,” Journal of Perinatology, vol. 36, no. 8, pp. 606–611, 2016.
View at: Publisher Site | Google Scholar
C. A. Combs, M. Gravett, T. J. Garite et al., “Amniotic fluid infection, inflammation, and colonization in preterm labor with intact membranes,” American Journal of Obstetrics and Gynecology, vol. 210, no. 2, pp. 125.e1–125.e15, 2014.
View at: Publisher Site | Google Scholar
T. Myntti, L. Rahkonen, M. Tikkanen, J. Paavonen, and V. Stefanovic, “Vaginally obtained amniotic fluid samples in the diagnosis of subclinical chorioamnionitis,” Acta Obstetricia et Gynecologica Scandinavica, vol. 95, no. 2, pp. 233–237, 2016.
View at: Publisher Site | Google Scholar
T. Myntti, L. Rahkonen, A. Pätäri-Sampo et al., “Comparison of amniotic fluid matrix metalloproteinase-8 and cathelicidin in the diagnosis of intra-amniotic infection,” Journal of Perinatology, vol. 36, no. 12, pp. 1049–1054, 2016.
View at: Publisher Site | Google Scholar
N. Hofer, E. Zacharias, W. Müller, and B. Resch, “An update on the use of C-reactive protein in early-onset neonatal sepsis: current insights and new tasks,” Neonatology, vol. 102, no. 1, pp. 25–36, 2012.
View at: Publisher Site | Google Scholar
D. Garry, R. Figueroa, M. Aguero-Rosenfeld, E. Martinez, P. Visintainer, and N. Tejani, “A comparison of rapid amniotic fluid markers in the prediction of microbial invasion of the uterine cavity and preterm delivery,” American Journal of Obstetrics and Gynecology, vol. 175, no. 5, pp. 1336–1341, 1996.
View at: Publisher Site | Google Scholar
P. C. Greig, J. M. Ernest, and L. Teot, “Low amniotic fluid glucose levels are a specific but not a sensitive marker for subclinical intrauterine infections in patients in preterm labor with intact membranes,” American Journal of Obstetrics and Gynecology, vol. 171, no. 2, pp. 365–371, 1994.
View at: Publisher Site | Google Scholar
K. J. Oh, K. H. Park, S.-N. Kim, E. H. Jeong, S. Y. Lee, and H. Y. Yoon, “Predictive value of intra-amniotic and serum markers for inflammatory lesions of preterm placenta,” Placenta, vol. 32, no. 10, pp. 732–736, 2011.
View at: Publisher Site | Google Scholar
T. Sorsa, L. Tjäderhane, Y. T. Konttinen et al., “Matrix metalloproteinases: contribution to pathogenesis, diagnosis and treatment of periodontal inflammation,” Annals of Medicine, vol. 38, no. 5, pp. 306–321, 2006.
View at: Publisher Site | Google Scholar
S. J. Fortunato, R. Menon, and S. J. Lombardi, “MMP/TIMP imbalance in amniotic fluid during PROM: an indirect support for endogenous pathway to membrane rupture,” Journal of Perinatal Medicine, vol. 27, no. 5, pp. 362–368, 1999.
View at: Google Scholar
E. Maymon, R. Romero, P. Pacora et al., “Evidence of in vivo differential bioavailability of the active forms of matrix metalloproteinases 9 and 2 in parturition, spontaneous rupture of membranes, and intra-amniotic infection,” American Journal of Obstetrics and Gynecology, vol. 183, no. 4, pp. 887–894, 2000.
View at: Publisher Site | Google Scholar
S. A. Kim, K. H. Park, and S. M. Lee, “Non-invasive prediction of histologic chorioamnionitis in women with preterm premature rupture of membranes,” Yonsei Medical Journal, vol. 57, no. 2, pp. 461–468, 2016.
View at: Publisher Site | Google Scholar
R. Romero, N. Kadar, J. Miranda et al., “The diagnostic performance of the Mass Restricted (MR) score in the identification of microbial invasion of the amniotic cavity or intra-amniotic inflammation is not superior to amniotic fluid interleukin-6,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 27, no. 8, pp. 757–769, 2014.
View at: Publisher Site | Google Scholar
B. R. Helmig, R. Romero, J. Espinoza et al., “Neutrophil elastase and secretory leukocyte protease inhibitor in prelabor rupture of membranes, parturition and intra-amniotic infection,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 12, no. 4, pp. 237–246, 2002.
View at: Publisher Site | Google Scholar
G. J. Locksmith, P. Clark, P. Duff, G. R. Saade, and G. S. Schultz, “Amniotic fluid concentrations of matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 1 during pregnancy and labor,” American Journal of Obstetrics and Gynecology, vol. 184, no. 2, pp. 159–164, 2001.
View at: Publisher Site | Google Scholar
N. Athayde, S. S. Edwin, R. Romero et al., “A role for matrix metalloproteinase-9 in spontaneous rupture of the fetal membranes,” American Journal of Obstetrics and Gynecology, vol. 179, no. 5, pp. 1248–1253, 1998.
View at: Publisher Site | Google Scholar
F. Ghezzi, M. Franchi, L. Raio et al., “Elevated amniotic fluid C-reactive protein at the time of genetic amniocentesis is a marker for preterm delivery,” American Journal of Obstetrics and Gynecology, vol. 186, no. 2, pp. 268–273, 2002.
View at: Publisher Site | Google Scholar
M. Öz, B. Polat, E. Özgü, K. D. Seçkin, C. Taşin, and N. Danişman, “Interleukin-6 and C-reactive protein levels in the amniotic fluid as indicators of preterm delivery in Turkish women,” Clinical and Experimental Obstetrics and Gynecology, vol. 42, no. 6, pp. 801–804, 2015.
View at: Publisher Site | Google Scholar
A. T. Dulay, I. A. Buhimschi, G. Zhao et al., “Compartmentalization of acute phase reactants Interleukin-6, C-Reactive Protein and Procalcitonin as biomarkers of intra-amniotic infection and chorioamnionitis,” Cytokine, vol. 76, no. 2, pp. 236–243, 2015.
View at: Publisher Site | Google Scholar
A. Malek, N. A. Bersinger, S. Di Santo et al., “C-reactive protein production in term human placental tissue,” Placenta, vol. 27, no. 6-7, pp. 619–625, 2006.
View at: Publisher Site | Google Scholar
B. H. Yoon, R. Romero, J.-Y. Shim, S.-S. Shim, C. J. Kim, and J. K. Jun, “C-reactive protein in umbilical cord blood: a simple and widely available clinical method to assess the risk of amniotic fluid infection and funisitis,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 14, no. 2, pp. 85–90, 2003.
View at: Publisher Site | Google Scholar
J. Hitti, P. Tarczy-Hornoch, J. Murphy, S. L. Hillier, J. Aura, and D. A. Eschenbach, “Amniotic fluid infection, cytokines, and adverse outcome among infants at 34 weeks' gestation or less,” Obstetrics and Gynecology, vol. 98, no. 6, pp. 1080–1088, 2001.
View at: Publisher Site | Google Scholar
Y. Maki, S. Furukawa, Y. Kodama, H. Sameshima, and T. Ikenoue, “Amniocentesis for threatened preterm labor with intact membranes and the impact on adverse outcome in infants born at 22 to 28 weeks of gestation,” Early Human Development, vol. 91, no. 5, pp. 333–337, 2015.
View at: Publisher Site | Google Scholar
R. P. Porreco, K. D. Heyborne, and H. Shapiro, “Amniocentesis in the management of preterm premature rupture of the membranes: a retrospective cohort analysis,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 21, no. 8, pp. 573–579, 2008.
View at: Publisher Site | Google Scholar
K. L. Archabald, I. A. Buhimschi, M. O. Bahtiyar et al., “Limiting the Exposure of select fetuses to intrauterine infection/inflammation improves short-term neonatal outcomes in preterm premature rupture of membranes,” Fetal Diagnosis and Therapy, 12 pages, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2017 Tarja Myntti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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