Open Journal of Obstetrics and Gynecology
 Vol.3 No.7(2013), Article ID:36247,5 pages DOI:10.4236/ojog.2013.37096

Low maternal leptin levels in preeclamptic women with fetal growth restriction*

Herman Sumawan1,2#, Benny Hasan Purwara1, Sofie Rifayani Krisnadi1

1Department of Obstetrics and Gynecology, Faculty of Medicine, Padjadjaran University/Hasan Sadikin Hospital, Bandung, Indonesia

2Department of Obstetrics and Gynecology, Faculty of Medicine and Health Sciences, Soedirman University, Purwokerto, Indonesia

Email: #h_sumawan@yahoo.com

Copyright © 2013 Herman Sumawan 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.

Received 4 July 2013; revised 2 August 2013; accepted 9 August 2013

Keywords: Leptin; Intrauterine Growth Restriction; Small for Gestational Age; Preeclampsia

ABSTRACT

Objective: We hypothesized that preeclamptic women with intrauterine growth restriction (IUGR) would have lower concentrations of leptin compared to women with normal fetal growth. Methods: A crosssectional study was performed in 20 cases of IUGR and 20 normal fetuses born to women diagnosed with preeclampsia. Blood samples were collected from mothers at term gestation and with fetal birth weight less than 2500 grams would categorized as IUGR. The subjects were recruited by consecutive sampling conducted in Hasan Sadikin Hospital and several network hospitals during the period of September-November 2012. Results: A significant difference (p = 0.015) in maternal serum leptin levels was found between IUGR (22.1 ng/ml) and normal fetuses (36.5 ng/ml). Serum levels of leptin in preeclamptic women with IUGR were lower than normal fetuses. Spearman correlation test between maternal serum leptin levels and birth weight in IUGR did not demonstrate a significant correlation, with r = −0.321 (p = 0.168). Conclusion: The maternal leptin concentrations in IUGR are lower than the normal fetus in preeclampsia cases, but there was not enough evidence to support that leptin is associated with birth weight in IUGR.

1. INTRODUCTION

Intrauterine growth restriction (IUGR) is associated with perinatal mortality and morbidity. The most widely used definition of IUGR is a fetus whose estimated weight is below the 10th percentile for its gestational age. At term, the cutoff birth weight for IUGR is 2500 g [1]. The prevalence of IUGR in the world is 6 times higher in developing countries, 75% of which are located in Asia [2]. In Indonesia, the average prevalence from 4 centers of Maternal-Fetal Medicine during the period from 2004 to 2005 was 4.4%, with the highest prevalence (6.44%) reported in Sardjito Yogyakarta Hospital [3]

Leptin is a 167-amino acid protein, the product of the obese (ob) gene, mainly produced by fat cells [4]. Leptin is a peptide hormone regulating the energy homeostasis, reproductive function and immunologic reaction, and produced in the adipose tissue of non-pregnant women. During pregnancy, it is produced primarily by placental trophoblast cells and 95% is present in the maternal circulation [5,6].

Leptin concentration increases significantly in early pregnancy and reached 30% higher at 12 weeks of gestation compared with pregravid [6]. The relationship between maternal leptin levels and the fetal growth is not yet determined; whereas, fetal leptin concentrations represent the fetal adiposity. Abnormal increases in serum leptin production by the placenta during pregnancy illustrate the response to hypoxia due to ischemia placental trophoblast as observed in preeclampsia [6,7].

This situation is similar to that occurring in IUGR, where increased leptin is suggested to promote the mobilization fat reserves to improve the availability and support the transplacental transfer of lipid substrate and angiogenesis; leptin has the ability to enhance the transport of amino acids in the placenta [8,9]. Increased availability of nutrients is consistent with the observation that despite the decrease in placental perfusion, only one-third of neonates born from preeclamptic women have IUGR. In other words, preeclampsia is associated with the signal of fetus-placenta to increase the availability of nutrients and leptin production is the appropriate solution [10]. Recent studies regarding maternal leptin levels and fetal weight showed inconsistent results; leptin is associated with maternal morbidities, body mass index (BMI), smoking habits, as well as other complications [11-13]. This study aimed to determine the role of leptin in the growth of fetuses in mothers with preeclampsia. We evaluated maternal serum leptin in two groups: preeclampsia with and without IUGR.

2. SUBJECTS AND METHOD

The study is an observational analytic study with cross sectional method to compare the differences of maternal serum leptin levels in fetuses with normal growth and IUGR in preeclampsia, as well as to measure the magnitude of correlation of maternal serum leptin levels with fetal birth weight in preeclampsia. The study was conducted at the Department of Obstetrics and Gynecology RSHS Bandung and several network hospitals in West Java (Ujung Berung Hospital, Soreang Hospital, Astana Anyar Hospital, and Cibabat Hospital) between September-November 2012. It has received ethical approval from the Faculty of Medicine, University of Padjadjaran Bandung.

Subjects are pregnant women with single live fetus, who was diagnosed with preeclampsia (systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg and the urine protein + or more), gestational age limit 37 - 42 wks, had a normal BMI before pregnancy, did not have any co-morbidities such as heart failure, pulmonary tuberculosis, systemic lupus erythematous and diabetes mellitus, had no history of smoking before or during pregnancy and there were no birth defects in the fetus. Clinical characteristics of participating pregnant women are presented in Table 1.

Maternal blood samples (approximately 5 cc) were taken during labor, inserted into a sterile tube, centrifuged at 3000 rpm for 15 min, and then frozen at −20 Co. Leptin measurement was performed using Elisa reagent kit from R & D system. Intra-assay and inter-assay precisions for leptin measurement are 3.8% and 5%, respectively. All infants born were recorded; infants born at less than 2500 grams were assigned into IUGR group and those at more than 2500 grams were allocated into normal fetuses group, resulting in 20 samples for each group. Maternal data including parity, age, systolic and diastolic blood pressure, proteinuria and maternal BMI before pregnancy was obtained from patient records antenatal visit and BMI at the time.

Statistical analysis: the data was analyzed using SPSS for Windows version 18.0. This study used a nonparametric method after the data obtained did not show a normal distribution. Analysis of the differences was performed using the Mann-Whitney test and correlation for further assessment using the Spearman rank test.

Table 1. Characteristics of pregnant women with IUGR and normal fetus.

*Significant (p < 0.05).

3. RESULT

There was no statistically significant differences in the characteristics between the subjects in IUGR and normal fetal growth groups (n = 20 in each group) who met the inclusion criteria in Hasan Sadikin Hospital and network hospitals, including for maternal age (p = 0.255), parity (0.389) and BMI before pregnancy (p = 0.351) and during pregnancy (p = 0.266).

Table 1 shows the comparison of characteristics of infant birth weight between the IUGR fetuses and normal fetuses. The average birth weight for the infants with IUGR and normal fetuses were 2085 (SD ± 300.9) and 3047 (SD ± 367.13), respectively. We did find that systolic and diastolic blood pressure in IUGR group was not significantly different with normal fetus group. Table 2 shows that the average leptin level of IUGR group (22.9 ± 16.8 ng/ml) was lower than normal fetuses group (36.21 ± 17.0 ng/ml). The median leptin level of IUGR and normal fetuses were 16.09 ng/ml and 34.43 ng/ml, respectively. The Mann-Whitney test showed a statistically significant difference (p = 0.015) between the leptin concentrations in IUGR and normal fetuses. Table 3 shows the results of the statistical test

Table 2. The maternal serum leptin levels normal fetus and IUGR.

*Significant (p < 0.05).

Table 3. Correlation between leptin levels and birth weight infants.

with Spearman correlation test at the 95% confidence level indicates that there is no significant correlation between leptin levels with birth weight infant (r = −0.321; p = 0.168).

4. DISCUSSION

The result of this study showed that leptin levels in normal growth fetuses at term gestational age was 36.21 (SD ± 17.0) with a mean fetal weight of 3047 grams. These results are consistent with previous researches that showed that the levels of leptin in maternal preeclampsia was 35.8 (SD ± 22.0) with mean birth weight of 3150 grams [14]. Other previous studies showed various results of maternal plasma leptin levels in preeclamptic pregnancy at term, with the mean of 45.6 (32.4 to 60.4) ng/mL [6]; 47.8 ± 6.9 ng/mL [15], and 27.13 (14.4 to 49.5) ng/mL [16].

The values of leptin levels found in our study [22.9 (SD ± 6.8)] is lower than in a previous research. They found a higher mean maternal leptin levels in preeclampsia with IUGR at 26.5 (SD ± 3.8) ng/mL, with the average BMI of 30.3 kg/m2 (obese category) during the third trimester, which is a higher BMI compared the index in our study, 27.3 kg/m2 (during pregnancy) and 22.03 kg/m2 (pre-pregnancy) [17].

The pre-pregnancy BMI has an effect on maternal leptin levels and its effect seems to be weaker during pregnancy. In the non-pregnant state, the level of leptin produced by adipose tissue is directly related to BMI and the leptin level is increased in women with insulin resistance. Leptin clinically represents the adipose reserves in the human body [18-20]. Levels of leptin in pregnancy are lower on women with normal BMI than on women with overweight or obese [21]. In the current study, the influence of BMI on leptin level had reduced, because BMI between sample was similar.

A prospective study showed that lower leptin levels in the early trimester poses a higher risk of fetal weight growth failure and having a smaller fetus [22]. Another research reported that mothers of small for gestational age (SGA) infants had lower leptin level than the mothers of infants with appropriate weight-for-gestational age infants [10,11]. Lower leptin levels in IUGR suggests the possibility of leptin expression failure in the placenta as the response to hypoxia that should spur the production of leptin to improve the lack of uteroplacental perfusion. Placental leptin expression and growth factors level were lower in small for gestational age infant compared to normal infants [10]. We speculate that low leptin levels would lead to the impairment of the compensation mechanism to increase nutrients transfer in the placenta which would result in restricted fetal growth. The effects of leptin on growth and development in the fetus, may be celland tissue-specific rather than on general body growth and size [9].

Conflicting results have been reported from leptin studies that compare pregnancies with IUGR and pregnancies with normal fetal growth. Some studies showed no significant differences in leptin levels between the two groups [15,23,24]. Several studies reported that mothers of a SGA infants had higher leptin levels compared mothers of normal birth weight infants [12,17,25,26]. It may be explained by the notion that leptin levels were higher in mothers with preeclamptic SGA infants compared to normal infants, due to the occurrence of chronic hypoxia that causes the disorder to affect the nutrition and eventually results in IUGR. Placental hypoperfusion causes local hypoxia, which triggers increased production of leptin by the placenta [25,26]. However, worsening of placental function sometimes advances rapidly in preeclamptic women accompanied with elevated blood pressure. In that condition, increased placental leptin production may take place, while fetal growth restriction may not become apparent in a short duration. Otherwise in women with slowly progressing disease, maternal plasma leptin levels may not increase so highly in spite of more apparent restriction in fetal growth [25].

Relations between leptin levels and birth weight were reported in Nezar’s studies, which suggested that leptin level is negatively correlated with fetal weight [17]. However, in our study found no significant correlation between maternal leptin levels and birth weight as shown in Table 3. Factors that influence these results include differences in the number and characteristics of the sample, the sample selection criteria in full-term pregnancies; different BMI. The limitation in our study was ability to confirm that the restricted growth by serial ultrasound diagnosis was not available.

Based on the results of this study we concluded that the levels of leptin of preeclamptic women with IUGR fetuses is lower than those with normal fetuses; thus, it can be used as a complement to indicate fetal growth, although a direct correlation between leptin and fetal growth still has not been proven unequivocally. Further research, especially serial examinations of leptin with serial biophysical fetal during pregnancy, would be a substantial additional information in the pathogenesis of fetal growth.

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NOTES

*All the authors declare that they have no conflicts of interest.

#Corresponding author.

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