Corresponding author: Chang Won Choi, MD, PhD. Department of Pediatrics, Seoul National University Bundang Hospital, 82 Gumi-ro 1173 Beon-gil, Bundang-gu, Seongnam 13620, Korea. Introduction
Chorioamnionitis is a maternal inflammatory response that involves neutrophil infiltration in the fetal membranes or placenta with or without a fetal inflammatory response1). Chorioamnionitis has been known to be a major risk factor for preterm delivery and prematurity-associated morbidities2,3,4). Bronchopulmonary dysplasia (BPD) is one of the major morbidities of preterm infants and represents a chronic lung disease that develops exclusively inpreterm infants5). The association of chorioamnionitis and BPD has been reported in animal and human studies6,8,9). However, there are also not a few studies that reported conflicting results and the evidence of publication bias, which lead to continuing controversies on the relationship between chorioamnionitis and BPD9,10). In this review, the relationship between chorioamnionitis and BPD and the background for the controversy on this issue will be disussed. Because clinical chorioamnionitis can reflect other conditions than true inflammation in the fetal membranes, placenta, and fetal tissue, only histologic chorioamnionitis will be discussed in this review.
The effect of chorioamnionitis on the development of BPD
1. Animal studies
There have been a number of animal studies which demonstrated an association of chorioamnionitis and BPD11). The sheep and rodent models of BPD had been established and the pathogenetic role of chorioamnionitis on the development of BPD has been searched in these animal models12,13,14). The chorioamnionitis or intra-amniotic inflammation has been induced by intra-amniotic lipopolysaccharide (LPS) injection or direct Ureaplasma urealyticum inoculation into amniotic sacs. The experimental chorioamnionitis consistently resulted in fetal lung maturational responses which can be reflected by a reduction of the alveolar septal thickness, restructuring of the double capillary system to a single capillary system, or increased surfactant production15). However, these maturational responses were frequently followed by a disturbed lung development: fewer and larger distal airspaces resembling BPD of human preterm infants13). In a newborn rat model of BPD devised by the author, experimental chorioamnionitis induced by intra-amniotic LPS not only directly inhibited alveolarization but also amplified the inhibitory effect of hyperoxia on alveolarization14). However, in the same animal model, experimental chorioamnionitis protected the lungs against BPD triggered by postnatal systemic inflammation15), as shown in Fig. 1. In a preterm fetal sheep model, intra-amniotic Ureaplasma injection decreased elastic foci and increased smooth muscle around bronchioles and pulmonary arterioles which are distinctive pathologic findings seen in human BPD16,17,18). Taken together, these animal studies supports that chorioamnionitis accelerates lung maturation but eventually disrupt normal lung development resulting in BPD.
2. Human studies
Despite not a few studies supporting the role of chorioamnionitis on the development of BPD, controversies continue on this issue2,3,4,19,20). The chorioamnionitis has been known to protect against respiratory distress syndrome (RDS). The beneficial effect of chorioamnionitis on the incidence of RDS has been shown under the exposure to antenatal corticosteroid3,4,21). However, this beneficial effect of chorioamnionitis on RDS may render the premature lungs more vulnerable to various postnatal injuries6,7,22,23,24). The chorioamnionitis increased the risk of BPD with a synergism with patent ductus arteriosus and mechanical ventilation8,24). On the contrary, funisitis, a type of chorioamnionitis primarily involving umbilical cord, has been shown to protect against BPD in a study10). A recent meta-analysis by Hartling et al.25) which included more than 15,000 infants demonstrated that chorioamnionitis is significantly associated with the development of BPD. In a retrospective cohort study by the author, while all types of chorioamnionitis decreased RDS, high grade amnionitis increased BPD26). However, in other cohort studies, chorioamnionitis was not associated with the development of BPD10,27). As in animal model of BPD, chorioamnionitis increased the development of BPD by adversely affecting various postnatal injuries including RDS, mechanical ventilation, and sepsis in the clinical observations8,23,28). This can also be expressed as chorioamnionitis may make the preterm lungs to be more susceptible to postnatal injuries resulting in amplified inflammation and ultimately BPD29). However, there are a number of confounding factors that can be involved between chorioamnionitis and BPD. The diversity and uncertainty of diagnostic criteria of chorioamnionitis and BPD and inhomogeneity of the study populations also matter in investigating the relationship between chorioamnionitis and BPD. All these factors make the research for the role of chorioamnionitis in the development of BPD challenging.
Background for the controversies on the role of chorioamnionitis in the development of BPD
1. Definition of chorioamnionitis
The diversity and uncertainty of the definition of chorioamnionitis may partly responsible for the controversies on the role of chorioamnionitis in the development of BPD. A recent systemic review of 59 studies reported that the definition of chorioamnionitis varied across the studies25). Different definitions of chorioamnionitis may confound the actual effect of chorioamnionitis on BPD. Furthermore, because chorioamnionitis can vary in location and extent, it is too insufficient to identify the relationship between chorioamnionitis and BPD, just to see if there is a chorioamnionitis or not. In this regard, the author investigated the relationship between chorioamnionitis on BPD using the definition of chorioamnionitis that reflects the location and extent of the inflammation26). In this study, the chorioamnionitis was divided into four categories according to the location of inflammation: any chorioamnionitis; amnionitis; funisitis; amnionitis plus funisitis. Each category was further divided into high and low grades according to the extent of inflammation. The results of the study revealed that high grade amnionitis increases BPD. Because amnion lines the amniotic cavity, high grade amnionitis may indicate strong chemotactic stimuli within the amiotic cavity that will consequently results in fetal pulmonary inflammation and fetal lung damage. In this regard, the relationship between high grade amnionitis and BPD may be biologically plausible. Large scale cohort study that uses unified but subdivided criteria of chorioamnionitis will be needed to clarify the actual relationship between chorioamnionitis and BPD.
2. Variations in the definition of BPD
It is important to have clear definition of BPD to compare outcomes in clinical trials or quality improvement and to identify risk factors in epidemiological studies. Which definition of BPD is used will also affect the result of the investigation for the relationship between chorioamnionitis and BPD. The requirement of supplemental oxygen has been used as a surrogate for pulmonary dysfunction seen in BPD. The duration of oxygen dependency and the extent of supplemental oxygen needed to maintain adequate arterial blood oxygen saturation have been used to define BPD and its severity. However, there has been a lack of uniformity in the definition of BPD among clinical trials and epidemiological studies on BPD30). Moreover, the indications for oxygen supplementation vary from center to center and from person to person in a center. Among the definitions of BPD, the need for supplemental oxygen at 36 weeks postmenstrual age without a physiologic test confirming the oxygen dependency is the most frequently used definition of BPD in clinical trials and epidemiologic studies31). However the incidence of BPD diagnosed by this definition can be influenced by different strategies for oxygen supplementation which will be different from center to center and from person to person in a center. Different arterial blood oxygen saturation targets, different ventilatory strategies, and different medication practice will lead to different oxygen supplementation strategies. In interpreting the results of the studies of the relationship between chorioamnionitis and BPD, the definition of BPD used in the individual study should be taken into account.
3. Variations in the study population
The incidence of chorioamnionitis and BPD can vary according to the subject population studied. The lower the gestational age and birth weight, the higher the incidences of chorioamnionitis and BPD. Because the relationship between chorioamnionitis and BPD can also be influence by gestational age and birth weight, it is important to interpret the results of the studies on the relationship between chorioamnionitis and BPD considering the characteristics of the study population. The effects of chorioamnionitis on the development of BPD have been studied in different population groups11). Different study population may be one of the causes of controversy on the relationship between chorioamnionitis and BPD.
Which contributes more: inflammation or infectious microorganisms?
The chorioamnionitis can be caused by a variety of stimuli. Most cases of chorioamnionitis are associated with intrauterine infections caused by genital mycoplasma like U. urealyticum11). A recent systemic review reported that the exposure to Ureaplasma increased the incidence of BPD32). Ureaplasma has been believed to contribute to the development of BPD by dysregulating inflammatory responses in the immature lungs resulting in aberrant lung development and fibrosis33). Although intrauterine exposure to Ureaplasma is related to chorioamnionitis, the presence of Ureaplasma does not always overlap with chorioamnionitis34). A simple colonization of Ureaplasma in the fetal membranes or placenta can occur without inducing chorioamnionitis35). It is not yet known which of chorioamnionitis or Ureaplasma infection contributes more to the development of BPD. In studying the relationship between chorioamnionitis and BPD, simply examining whether or not the chorioamnionitis is present can lead to incorrect conclusions. Both the type of microorganisms causing chorioamnionitis and the extent of chorioamnionitis by those microorganisms should be evaluated to clarify the actual relationship between chorioamnionitis and BPD.
Ureaplasma and BPD
Microorganisms are found in approximately 75% of the placenta with chorioamnionitis36). Most common microorganism isolated from the placenta or amniotic fluid of pregnant women with chorioamnionitis is Ureaplasma species34). The association of Ureaplasma colonization with BPD has been demonstrated in human neonates by several meta-analyses that included more than 40 individual studies32,37,38). In animal studies including mice, sheep, and nonhuman primates, in utero Ureaplasma infection has been shown to induce a sustained dysregulated inflammatory response in the immature lungs that results in impaired alveolarization and excessive collagen and elastic deposition39). Disrupted alveolarization and airway and pulmonary vascular remodeling is a pathologic hallmark of BPD. The most definitive evidence for the role of Ureaplasma in the development of BPD will be obtained through the trial of anti-Ureaplasma agent in Ureaplasma-infected subjects. If the anti-Ureaplasma treatment can reduce the incidence of BPD in Ureaplasma-infected animals or human infants, the role of Ureaplasma in the development of BPD will be proven. In the Rhesus monkey intrauterine Ureaplasma infection model, azithromycin delayed onset of labor, eradicated the infection, and prevented fetal lung injury40,41). However, prolonged antenatal exposure to Ureaplasma infection resulted in persistent chorioamnionitis and fetal lung injury in a sheep model despite a successful eradication of Ureaplasma by azithromycin or solithromycin42). These results suggest that early detection of Ureaplasma infection will be essential for optimal timing of anti-Ureaplasma treatment to prevent fetal lung injury or BPD in the fetus or preterm infants infected with Ureaplasma. In human preterm infants, prophylactic azithromycin decreased the incidence of BPD. However, therapeutic macrolides did not decrease the incidence of BPD among Ureaplasma-positive preterm infants43). At the moment, there is not enough evidence that the eradication of Ureaplasma results in a reduction of BPD. A phase IIB, placebo-controlled, randomized trial of the multi-dose azithromycin regimen in preterm infants is currently underway. The result of this clinical trial will provide us with the information on the effect of azithromycin on the BPD and long-term neurodevelopmental outcomes39).
Conclusions
The results of a number of animal experimental and human epidemiologic studies suggest that chorioamnionitis affects the development of BPD directly or indirectly. However, there are not a few limitations in the individual study. Not-unified definitions of the chorioamnionitis and BPD, differences in the study populations, and the proportion of contribution between inflammation and infectious microorganisms should be considered in interpreting the results of these studies. The results of the clinical trials of anti-Ureaplasma or anti-inflammatory treatment for pregnant women with chorioamnionitis or preterm infants who have been exposed chorioamnionitis will provide answer to the controversies on causal relationship between chorioamnionitis and BPD and a novel prophylactic strategy against BPD based on that relationship.
PDF Links
PubReader
ePub Link
XML Download
PubMed
Download Citation
