Introduction
Common pregnancy complications include small for gestational age (SGA), preeclampsia (PE), and gestational diabetes mellitus (GDM). The incidence of complicated pregnancies has gradually increased by 5% to 10% for SGA [
1], 2% to 5% for PE [
2], and 2% to 13% for GDM [
3] worldwide. Recent studies have shown that pregnancies can be complicated by placental pathologies and fetal growth changes. The placenta, a temporary organ responsible for controlling nutrition from the mother to the fetus, has been observed to influence birth weight [
4], and its weight has been shown to be directly associated with birth weight [
5,
6]. Some studies suggest that placental factors play an important role in fetal growth restriction and all macroscopic and microscopic pathological changes point towards reduced blood flow caused by vascular damage [
1]. Roberts and Lain [
2] showed that PE was secondary to the interactions of reduced placental perfusion with diverse maternal factors that alter endothelial function. Other studies suggest that placental pathological changes in diabetic women, such as significant thickening of trophoblastic basal membranes, separation of capillary basal membranes in basal capillaries, distention and proliferation of endothelial cells, disarrangements of perivascular space, and decrease of terminal villous vascular surface, are significant factors contributing to fetal growth in pregnancies complicated by diabetes mellitus [
7].
Placental pathologies can be classified as functional or morphological. Functional changes are related to protein alteration, receptor expression, cytokines, chemokines, and hormones [
8,
9]. Conversely, morphological changes are detected by measuring placental weight, placental volume, birth weight/placental weight ratio (BPW), and the microscopic shape of placental villi. Recent studies have investigated the association between placental morphological changes and complicated pregnancies. Janthanaphan et al. [
10] showed that placental weight increased with birth weight, and the BPW decreased slightly with advancing gestational age in normal pregnancies. In diabetic pregnancies, placental weight as well as the BPW was higher than that in non-diabetic pregnancies [
11]. Bortolus et al. [
12] showed that the mean placental weight from large for gestational age (LGA) pregnancies was significantly increased compared with that from SGA pregnancies, whereas the placental ratio (BPW) tended to increase in LGA pregnancies compared with that in SGA pregnancies. Some researchers have compared placentas from control, intrauterine growth restriction (IUGR), PE without IUGR, and PE with IUGR pregnancies based on microscopic findings such as villous membrane exchange surface area, villous membrane thickness, and villous membrane diffusive conductance [
13].
Thus far, studies investigating the relationship between placental morphological changes and fetal growth in complicated pregnancies have been fragmentary, and lacked a systematic approach and comparisons between different groups of complicated pregnancies. Considering the role of the placenta in fetal growth, placental morphological characteristics such as placental weight, placental volume, and its ratio with birth weight could have significance in complicated pregnancies. This study aimed to evaluate the placental weight, volume, and density, and compare the significance of placental ratios in complicated pregnancies.
Results
From August 2005 through July 2013, 254 pregnant women were enrolled in this study. Participants were divided into four groups: control (n=87), SGA (n=37), PE (n=102), and GDM (n=33). Maternal characteristics and blood laboratory values in each group are shown in
Table 1. Blood pressure and blood laboratory values significantly differed in the PE group compared with those in the other groups. Birth weight, placental parameters (placental weight, volume, and density), BPW, and BPV in each group are shown in
Table 2. While the placental weight and volume in the SGA and PE groups were smaller than those in the control group, the placental weight and volume in the GDM group did not significantly differ from those in the control group. However, the placental density did not significantly differ between the control and complicated pregnancies. In control and complicated pregnancies, the placental weight is positively correlated with the birth weight (
Fig. 2). There was no difference in the BPW and BPV between the control and SGA groups. However, compared with the control group, BPW and BPV were lower in PE group, and higher in the GDM group.
The demographic and clinical data were compared between the PE without IUGR and PE with IUGR groups, as shown in
Table 3. Although blood pressures and blood laboratory values did not statistically differ between the two groups, an increasing trend was noted in the PE with IUGR group. Positive correlations between birth weight and placental weight in the PE without IUGR and PE with IUGR groups are shown in
Fig. 3. We compared the placental parameters, BPW, and BPV between these two groups (
Table 4). Although the placental weight and volume were lower in the PE with IUGR group, the placental density and the BPW and BPV ratios remained unchanged.
Discussion
In this study, the placental morphological characteristics and ratios were compared between control pregnancies and pregnancies complicated with SGA, PE, and GDM. Birth weight, placental weight, and placental volume were lower in the SGA and PE groups and higher in the GDM group than in the control group. The placental density, BPW, and BPV described in this study have rarely been evaluated in placental morphological studies. In this study, new parameters were evaluated to allow comparisons between groups and to evaluate placental function in complicated pregnancies. Placental density indicates placental structural characteristics, whereas the BPW and BPV indicate placental function calculated using the birth weight per unit weight or placental volume. One study showed that compared with the group with normal BPW ratios, those in the high BPW group had increased rates of admission to the neonatal intensive care unit, Apgar scores of <7 at 5 minutes, breech presentation, and delivery by caesarean section [
16]. Although complicated pregnancies may be associated with placental functional and morphological pathologies, no difference in placental density was found among groups in this study. In other words, placental density is not affected by the type of complicated pregnancy. BPW and BPV were similar in the control and SGA groups, but lower in the PE group and higher in the GDM group than in the control group.
Some studies showed the relation between placental volume and birth weight. Higgins et al. [
17] showed an association between maternal diabetes and increased terminal villous volume by stereological study of the placenta in type 1 and type 2 diabetes. One study revealed that first trimester placental volume is strongly associated with fetal and placental growth [
18]. However, studies for placental volume are limited to first trimester data, ultrasonographic results, and microscopic findings. To our knowledge, this is the first study providing data of birth weight/placental volume ratio.
In SGA pregnancies, the placental weight and birth weight were lower than those in control group, but there were no differences in placental density, BPW, and BPV. These results suggest that the SGA may not be caused by functional change in the placenta, but external obstetric factors such as uterine anomalies, genetic constitution, hypertension, malnutrition, anemia, and smoking. Some studies have shown that most SGA pregnancies were not associated with placental pathologies, and may be the result of fetal malnutrition, maternal anemia, and smoking [
19,
20,
21,
22,
23]. In PE pregnancies, birth weight, placental weight, and placental volume, as well as BPW and BPV, were lower than those in control group. This suggests a decrease of both placental and fetal size, as well as the activity of fetal growth per unit tissue of placenta. This finding can be explained by a reduction in placental function. The PE group was divided into two groups, PE without IUGR and PE with IUGR to evaluate the independent IUGR effect in the PE group. Both the PE without IUGR and PE with IUGR groups had decreased placental and fetal size, but showed no difference in BPW and BPV as much alike as control and SGA groups have differences only in birth weight and placenta weight. So, we can hypothesize that IUGR in PE pregnancies may originate from non-placental causes. Kovo et al. [
24] explained morphological changes in the placental villi in IUGR pregnancies complicated by pregnancy-induced hypertension and normotensive IUGR. This study showed that placental lesions in pregnancies complicated by hypertensive disorders were different from those in normotensive IUGR pregnancies. In the GDM group, the placental parameters (placental weight, volume, and density) did not differ from those in the control group. However, placental ratios (BPW and BPV) were significantly increased in the GDM group compared with those in the control group. Except for placental parameters, the fetal size as well as the fetal growth activity per placental unit tissue increased. Therefore, placental function in GDM pregnancies is increased, unlike in PE pregnancies, and excessive placental growth leads to fetal growth.
Previous studies retrospectively measured placental weight and fetal birth weight after delivery to predict adverse pregnancy outcomes. Our findings suggest that disease-specific BPW and BPV, as well as placental density, can be used to predict pregnancy complications before delivery. For example, we can assume birth weight and placental volume measured by two-dimensional and three-dimensional ultrasonography before delivery can be used to predict pregnancy complications. If placental volume, estimated fetal body weight (EBW), and estimated BPV (EBPV) are lower than those observed in control pregnancies, we can predict the probability that this pregnancy will be complicated by PE. If placental volume and EBW are lower and EBPV is similar, we can predict that the pregnancy will be complicated by SGA. Lastly, if EBW and EBPV are increased compared with control group and placental volume is similar, the pregnancy could be complicated by GDM. Future studies need to focus on confirming these findings. In addition, further research on functional changes associated with placental pathologies needs to be considered.
This study has some of limitations. The number of participants in each group was slightly heterogeneous. The median pregnancy duration in the PE group was 35 weeks' gestation, which is different from other groups. All cases enrolled in this study were not obtained during the same period. Until now, there have been no definite methods to measure the placental profiles such as weight, size, volume, and density. Considering the placental volume, there is one known method that after the placenta is soaked in water, the volume of overflowed water is measured as a placental volume. However, this method has also some limitations. So, we tried to measure the volume of placenta arithmetically and geometrically. There is a possibility that the calculated placental volume is not same to true volume of placenta. But, the calculated placental volume is well correlated with placental weight, and can be used for comparison among the groups. Though the preeclamptic placentas were measured by three persons due to long study period, the other placentas were evaluated by one. Because we don't have data for interobserver and intraobserver variability, we will study for the variability in the placental morphologic measuring in the near future. Strictly speaking, the control group is not the control group. Though the control group includes some preterm delivery cases, the placentas with chorioamnionitis or abnormal shape were excluded. Despite these weaknesses, the systematic approach and placental morphological comparisons included in this study contribute to understanding complicated pregnancies.
In conclusion, our study suggests that placental weight, volume, and density, as well as the birth weight and associated ratios, are helpful in understanding the pathophysiology of complicated pregnancies. Moreover, they can be used to predict pregnancy complications.