The relation between serum levels of epidermal growth factor and necrotizing enterocolitis in preterm neonates

Article information

Korean J Pediatr. 2019;62(8):307-311

Publication date (electronic) : 2019 March 15

doi : https://doi.org/10.3345/kjp.2018.07108

Heba Mostafa Ahmed, MD^,1, Nsreen Mostafa Kamel, MD²

¹Department of Pediatrics, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt

²Department of Clinical and Chemical Pathology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt

Corresponding author: Heba Mostafa Ahmed, MD Departments of Pediatrics, Faculty of Medicine, Beni-Suef University, Mohammed Hassan street, Beni-Suef governate, Egypt Tel: +201001516641 Fax: +201001516641 E-mail: heba_most@yahoo.com

Received 2018 September 22; Revised 2019 February 1; Accepted 2019 March 14.

Abstract

Introduction

Necrotizing enterocolitis (NEC) is one of the most serious complications of prematurity, with a prevalence of 7% in very low birth weight infants and mortality between 20% and 30% [1]. The high rate of morbidity and mortality is due to the multifactorial pathogenesis of NEC. There is no a clear mechanism involved as a cause of NEC, only several factors that contributes to it [2]. These factors include undeveloped gastrointestinal mucosal barrier, immature innate and humoral immunity, uncoordinated GIT movement, and the overgrowth of pathogenic bacteria [3]. There are many risk factors can contribute to the development of NEC as prematurity, formula feeding, hypoxic-ischemic insult, and abnormal bacterial colonization of the gut. Yet, no single risk factor is crucial, and the mechanisms by which they precipitate NEC are mostly unclear [4]. Initial management of NEC is generally supportive and includes stopping enteric feedings and providing total parenteral nutrition, continuous nasogastric suctioning with intestinal decompression, and administration of broad-spectrum antibiotics [5]. NEC occurs with variety of severity ranging from a mild form that improves with antibiotics and discontinuation of oral feedings (medical NEC) to a severe form that leads to intestinal perforation, peritonitis, and eventually death [6]. Approximately 20%–40% of all infants diagnosed with NEC require surgical intervention [7]. Many studies had have attempted to find out biomarkers for the early detection of NEC [8]. Epidermal growth factor (EGF) is a 50-kDa multifunctional protein that has antiangiogenic, antitumorigenic and neurotrophic functions [9]. It belongs to a vast family of peptides (transforming growth factor-alpha, amphiregulin, heparin-binding EGF, epiregulin, betacellulinn and neuroregulin, among others) which provoke a variety of biological responses in the gastrointestinal tract, the majority of which involve regulation of cell replication and cell movement and survival. Also, it enhances the proliferation and differentiation of epithelial cells [10].

The aim of this study was to assess the relation between EGF serum level and the development of NEC in preterm neonates.

Materials and methods

This study was conducted between March 2015 and April 2017. One hundred thirty preterm neonates were included in the study and were divided into 3 groups; group 1 (40 preterms with NEC), group 2 (50 preterms with sepsis), and group 3 (40 healthy preterms as normal controls). Patient inclusion was established by the presence of signs specific for NEC by modified Bell’s criteria [11] or, for the sepsis group, by either clinical evidence of sepsis and/or positive blood cultures. Preterms with history of previous abdominal surgery, or a known congenital anomaly of the gastrointestinal tract or abdominal wall were excluded from the study. All included subjects were subjected to (1) full history taking stressing on gestational age (GA), sex, obstetrical history (mode of delivery), obstetrical problems placenta abnormalities, premature rupture of membranes, etc., (2) clinical examination including: general examination, local, physical examination and measurements (weight, length), and vital signs. Laboratory investigations included C-reactive protein (CRP), complete blood picture with differential counts, blood culture, sensitivity, and serum EGF levels. Erect abdominal X-ray and abdominal ultrasonography were done to cases with NEC then NEC group was divided accordingly to 2 subgroups (surgical NEC and medical NEC). To perform the multiple regression tests the included neonates are divided into 2 groups; group 1 patients without NEC, group 2 patients with NEC

The local ethical committee of Beni-Suef University Hospital approved the study protocol (approval number: 187-36) and a written consent was obtained from caregivers of the included neonates.

Results

There was no difference between the groups as regarding gender and GA. Age and body weight were significantly higher in control group than sepsis and NEC groups but no difference between sepsis and NEC groups. Hemoglobin levels and TLC were statistically insignificant between the 3 groups while NEC group had lower platelets levels than other groups. CRP was significantly higher in sepsis and NEC groups as compared to controls. EGF was significantly lower in the sera of NEC group (median [IQR], 9.6 [2–14]) as compared to both sepsis (median [IQR], 10.1 [8–14]) and control (median [IQR], 11.2 [8–14]) groups and there was no difference between control and sepsis groups (Table 1). Blood culture was positive in 100% of cases with sepsis while it was positive in 87% in NEC group. Sixty-two percent (25 cases) of NEC group had medical NEC while surgical NEC was reported in 38% (15 cases). On comparing medical and surgical NEC groups; GA, age, and body weight were significantly lower in surgical NEC group. EGF levels were lower in surgical NEC but it was statistically insignificant (Table 2). Binary logistic regression test was run to predict NEC based on EGF, GA, and sex. These variables statistically significantly predicted NEC, χ² (3, 130)=63.5, P<0.001, R²=0.75. There was a significant negative association between both EGF and GA as predictors of the development of NEC (β=-1.3, P< 0.001) and (β=-0.14, P=0.009) respectively. Sex has no influence on the prediction of development of NEC (Table 3). There was strong significant positive correlation between EGF and GA (r=0.7, P<0.001) (Fig. 1). ROC curves were used to define the possible value of serum EGF level below which NEC is highly suspected to occur. The area under the ROC curve of serum EGF levels was 0.92 (95% confidence interval, 0.83–0.97). The analysis rendered an optimal cutoff value of 8 pg/mL corresponding to 73.3% sensitivity and 98% specificity with positive predictive value (PV) of 95% and negative PV of 86.7 % (Fig. 2).

Table 1.

Demographic and laboratory data of the study groups

Table 2.

Comparison between the surgical and medical NEC groups

Table 3.

Binary logistic regression models for determining the relationships of EGF, sex, and gestational age with the development of NEC

Fig. 1.

Correlation between epidermal growth factor (EGF) levels and gestational age (GA). A significant positive correlation is observed between the EGF serum levels and gestational age, with the highest levels achieved at 230 days (33 weeks) of gestation.

Fig. 2.

Receiver-operating characteristic curve for the epidermal growth factor (EGF) cutoff value for the prediction of the development of necrotizing enterocolitis.

Discussion

The aim of this study was to assess the relation between EGF serum level and the development of NEC in preterm neonates and we found that patients with NEC had significantly lower serum levels of EGF indicating that EGF could be a reliable predictor of NEC in preterm neonates. The ultimate course of NEC cannot be predicted based on the clinical features alone so, efforts has been done for the identification of early biomarkers for NEC [11]. EGF is a protein secreted by the salivary glands, kidneys, liver, Brunner's glands of the duodenum, and Paneth cells of the small intestine [12]. EGF stimulates a variety of biologic responses, such as cell replication, cell movement, and cell survival [13]. EGF plays a major role in the intestinal barrier function, increases intestinal enzyme activity, and improves nutrient transport [14]. Many experimental studies had demonstrated the role of EGF as a regulator of epithelial paracellular permeability [15] and goblet cell and mucin production in the intestinal epithelium [16]. EGF also acts as a bacterial colonization inhibitor [17]. In our study, we found that patients with NEC had significantly lower serum levels of EGF than the other 2 groups indicating the critical role of EGF in maintaining the integrity and function of the intestinal wall and its deficiency contributes to the development of NEC in preterm newborns. Meanwhile, the absence of a significant difference between the sepsis group and healthy controls proves that EGF is not just a marker of a proinflammatory state and it is a specific marker for NEC. In addition, we found that EGF and GA had a significant negative association with NEC indicating that low EGF levels and smaller GA are significant risk factors for the development of NEC. Shin et al. [18] reported in their study that premature neonates with NEC have diminished levels of EGF in serum and saliva compared with healthy controls. The emerging need for early detection of NEC for early management and prevention of complications makes EGF a good marker for early detection of NEC. Despite statistically insignificant, the lower levels of EGF in surgical NEC group make it also a possible indicator for the course of the disease and disease severity. Our finding of strong positive correlation between EGF level and GA is in agreement with Hofmann and Abramowicz [19] who found that amniotic fluid contains significant concentrations of EGF that gradually increase during pregnancy, with the highest level achieved at the end of the normal gestation period explaining the association between NEC and prematurity. In this study, results showed that, using a cutoff value of <8 pg/mL, serum EGF level can be used to predict the development of NEC with an AUC of 0.92 and an optimized sensitivity of 73.3% and specificity of 98% with positive PV of 95% making EGF a reliable biomarker for the diagnosis of NEC.

The main strength of this study is that we have included patients with a relatively larger number of preterm neonates suffering of NEC as compared to some previous studies

Our study has some limitations. First, no comparison was made between EGF and other inflammatory markers (as erythrocyte sedimentation rate and procalcitonin). Second, single measurement of EGF levels was done, so serial measurement of EGF might be more useful.

In conclusion, our study highlights the role of EGF in NEC. EGF may be considered a reliable marker for NEC that could help in identifying diseased neonates. A value lower than 8 pg/L should raise the suspicion of NEC.

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