Can We Use Umbilical Cord Hydrogen Peroxide as an Early Predictor for Neonatal Hyperbilirubinemia?

Author's details

¹Department of Pediatrics, Faculty of Medicine, Minia University, Egypt

²Department of Pediatrics, Ministry of Health, Minia Governate, Egypt

³Department of Clinicalpathology, Faculty of Medicine, Minia University, Egypt

Date received: 27^th March 2020. Accepted 26^th April 2020.

Introduction

Hyperbilirubinemia is the most common clinical condition requiring evaluation and treatment in the newborn and is a frequent reason for hospital admission during the first week of life [1]. Neonatal hyperbilirubinemia is generally considered a benign self-limiting condition affecting more than 60% of healthy term and late preterm infants [2].  However, severe neonatal hyperbilirubinemia can lead to irreversible brain damage and kernicterus [3, 4]. Therefore, researchers have been enthusiastic about identifying early predictors of neonatal hyperbilirubinemia to assist in the early detection of neonates at high risk of severe hyperbilirubinemia and therefore neurological sequelae. A number of previous studies have highlighted the relationship between bilirubin and nitric oxide and reactive oxygen/nitrogen species [5].

Hydrogen peroxide (H₂O₂) is a freely miscible with water and apparently able to cross the cell membranes readily [6].

In low concentrations, it is not toxic for the body and it plays a certain role in the fulfillment of very important physiological functions, however if it is produced in excess, this free radical is harmful due to its cytotoxic properties [7].

The fetal tissues which are in a permanent state of low oxygenation during intrauterine life are subjected to oxidative damage by the increase of free radicals such as nitrous oxide (NO) and (H₂O₂). Soon after birth part of these free radicals is directed against the circulating erythrocytes and thrombocytes and may cause hemolysis and thrombolysis [8].

Hydrogen peroxide is a chemical compound with the formula (H₂O₂), it is one of the reactive chemical species containing oxygen, its normal blood level is between 2.53 and 5.75 umol/liter [8].

Oxygen free radicals have been incriminated as the causative mechanism for many neonatal diseases including broncho-pulmonary dysplasia (BPD), retinopathy of prematurity (ROP), necrotizing entero-colitis (NEC), intracranial hemorrhage (ICH) and hypoxic-ischemic encephalopathy (HIE) [9].

Given the relationship between bilirubin and hydrogen peroxide, which is one of reactive oxygen species, it could be suggested that if hydrogen peroxide levels in cord blood could be used to predict neonatal hyperbilirubinemia or not.

Aim of the work

The study aimed to answer if the cord blood hydrogen peroxide level can be used as an early predictor for neonatal hyperbilirubinemia or not and if there is a correlation between its levels and the severity of hyperbilirubinemia?

Subjects and Methods

This is a prospective comparative study included 59 full-term neonates delivered at Minia University hospital for gynecology & obstetrics and children during the period from June 2016 to December 2016. The patients were followed up for development of neonatal jaundice. Forty-one neonates developed neonatal jaundice, 14 of them were missed during the study follow-up, while 27 patients continued the follow-up and were assigned as patients (group I).  Eighteen neonates did not develop neonatal jaundice and were assigned as a control group (II).

Inclusion Criteria: full-term (37-42 weeks) neonates according to [New Ballard Score] for assessment of gestational age, birth weight 2500 – 4000 grams and Apgar score of ≥ 7 at 1 and 5 minutes of life.

Exclusion Criteria: Preterm neonates delivered before 37 weeks gestation, suspected patients of hemolytic diseases of the newborn, patients with cephalohematoma, cholestasis, major congenital or chromosomal abnormality and suspected sepsis, 

Both groups of patients and controls were subjected to: 

(1) Full history taking, including maternal medical problems, mode of delivery and Apgar score.

(2) Clinical examination including: assessment of gestational age using New Ballard Score, anthropometric measurements and systemic examination.

3. For all neonates, the following investigations were done 

1) Complete blood count using electronic counter Sysmex kx-21N

2) Reticulocyte count by Billiant Cresyl blue stain (supravital stain).

3) Maternal and neonatal blood group and Rhesus factor (Rh)

4) Serum bilirubin (total and direct) using modified diazo method (Bilirubin diamond diagnostic kits)

Principle:

Quantitative determination of bilirubin:

Two mls of cord blood and 2 mls of venous blood from all studied groups (patients and controls) at fifth and seventh days of life were collected for separation of enough serum required for the test. Bilirubin is converted to colored azobilirubin by diazotized sulfanilic acid and measured photo-metrically. The intensity of the color formed is proportional to the bilirubin concentration in the sample [10].

5) Serum hydrogen peroxide level.

Measurement of serum hydrogen peroxide levels (H₂O₂) from cord blood sample (5ml) for both groups (patients and controls) and from venous blood (3 ml) sample postnatal at fifth and seventh days of life for patients only (group I) using human hydrogen peroxide (H₂O₂) ELISA Kit, Glory Science co., Ltd

Principle of the test:

The kit is for the quantitative level of H₂O₂ in the sample, purified human H₂O₂ was adopted to coat micro titer plate, solid –phase antibody was made then samples or standards were added to wells with a labeled antibody specific to H₂O₂ then labeled HRP to well. The concentration of H₂O₂ in the samples is then determined by comparing the O.D. of the samples to the standard curve [11].

Statistical analysis:

SPSS (statistical package version 22) was used for statistical analysis of data. The p-value < 0.05 was considered the cut-off value of significance. Receivers Operating Characteristic (ROC) curve: was used to illustrate the diagnostic properties of a test on a numerical scale. Quantitative results were presented as mean ± SD while qualitative data were presented by frequency distribution as percentage (%). Correlation was performed by using Pearson correlation coefficient.

Results

There were no statistically significant differences between patients and controls regarding the age, sex, weight, mode of delivery, RBCs, reticulocyte count or platelets count, while there were significant lower levels of hemoglobin, total leucocytic count (TLC) and hematocrit levels in patients group than  controls  (p-values were p<0.001, p<0.001, p2O₂ levels as well as the bilirubin levels were higher in patients than controls (Table 1and figure 1). The bilirubin levels of cord blood, 5^th and 7^th days were higher in patients than controls with a peak level at the 5^th day of life (mean ±SD 13.8 ± 2.9 in patients)(Figure 2).

Significant positive correlations between cord blood H₂O₂ and cord blood bilirubin levels were present (r=0.81& p<0.001) (Figure 3) as well as between the cord blood H₂O₂ and bilirubin levels at the 5^th day of life (r=0.46& p<0.001) (Figure 4) and significant correlations between cord H₂O₂ and bilirubin levels at the 7^th day (r=0.60 & p<0.001) (Figure 5).

Moreover, there was a significant positive correlation between the 5^th day H₂O₂ and the 5^th day bilirubin levels (r=0.75& p<0.001) and a strong significant correlation between 7^th day H₂O₂and 7^th day bilirubin (r=0.94 & p= 0.001) (Table 3).There were non-significant correlations between H₂O₂ levels and each of weight and gestational age among patients (Table 4).

The sensitivity of the cord blood H₂O₂ in cases as a predictor to neonatal hyperbilirubinemia was 92.6% and the specificity was100% with a cutoff point >35 (p-value 0.001(Figure 6)

Discussion

Hyperbilirubinemia is the most common condition in neonates that requires medical attention. About 50% to 70% of term babies and 80% of preterm babies develop hyperbilirubinemia in the first week of life [12]. Although most neonates with hyperbilirubinemia are otherwise healthy, they need to be monitored. Hydrogen peroxide (H₂O₂) is the simplest peroxide present normally in the body [13].

Erythrocyte of newly born is sensitive to hydrogen peroxide and this sensitivity may be associated with deficiency of vitamin E or erythrocyte glutathione peroxidase or catalase [14].

If an excess of free radicals such as H₂O₂ is produced, as occurs in the case in the newborn, part of it is directed against the circulating erythrocytes and thrombocytes, and may cause hemolysis.

Early discharge of healthy term neonates is a common practice because of medical, social and economic constraints and in a significant number (6.5%) of neonates; the neonatal hyperbilirubinemia is a cause for readmission [15].

The American Academy of Pediatrics (AAP), 2004 [16] recom­mended that neonates discharged within 48 hours should have a follow-up visit after 2-3 days to detect significant hyperbilirubinemia and other problems.

Our results revealed that there were no significant differences between neonates with hyperbilirubinemia and controls regarding the age, sex, weight, and mode of delivery. These results agreed with the results of a study published in 2009 [17]. However, these results disagreed with  another study found that hyperbilirubinemia was more frequent in  boys than in girls and more in neonates delivered by  normal vaginal delivery than by Caesarean section with no explanation [18].

In this study, we found that the cord blood hemoglobin, TLC, and hematocrit were significantly lower in patients than controls and this may be attributed to hemolysis of RBCs in patients which cause bilirubin levels rise. These results were in concordance with the previous study [18] that found lower levels of hemoglobin, TLC in patients than controls.

The results of this study showed that levels of bilirubin in patients were more than in controls with a peak level at 5^th day (mean value of 13.8 mg /dl ± 2.9) and this was expected. Those results agree with other studiesreported that the peak of hyperbilirubinemia also was at the 5^th day with mean ± SD of 10.81±2.81mg/dl [19].

This study revealed significant higher levels of serum hydrogen peroxide in patients at 5^th and 7^th days with a peak level at 5^th day and mean ± SD 128± 37.7 pg/ml(P value<0.001) and there was a significant higher cord hydrogen peroxide levels in comparison to controls.

The results agreed partly with a study reported significant higher levels of hydrogen peroxide in hyperbilirubinemia in neonates at 3^rd and 5^th days more than in controls with a peak level at the 3^rd day [20].

In the present study, there were significant positive correlations between cord H₂O₂ and cord bilirubin levels (r=0.81& p<0.001) , between cord H₂O₂ and bilirubin at 5^th day (r=0.46& p<0.014) and between cord H₂O₂ and bilirubin in 7^th day (r=0.60 & p<0.001) respectively among patients. 

In the present study there was no-significant correlation between H₂O₂ levels and each of weight or gestational age among patients.

Chou et al, 2014 [20] recorded a sensitivity of 74.3% and a specificity 54.9% for cord blood hydrogen peroxide as a predictor for hyperbilirubinemia while in this study using cord blood hydrogen peroxide level of ≥35 pg/ml as a cut-off value, neonatal indirect hyperbilirubinemia can be predicted with a sensitivity of 92.6% and a specificity of 100% for the same markers.These results may be explained in the light of association between bilirubin concentrations and reductive and oxidative reactions.

It was found that the level of hydrogen peroxide increases rapidly during the first few days of life, parallel with the increase in bilirubin concentrations [17]. There is a strong correlation between hydrogen peroxide levels and bilirubin concentration. The increase in hydrogen peroxide levels is caused by increasing oxygen levels in the transition from fetal to the extra-fetal environment [17]. Hydrogen peroxide may damage red blood cell membranes, leading to the production of bilirubin [21]

The greater the reactive oxidative product, such as hydrogen peroxide level after birth, the more bilirubin is produced. Hence, we can measure hydrogen peroxide levels as an indicator of severe hyperbilirubinemia.

The significant positive correlations between cord blood hydrogen peroxide (H₂O₂) levels and bilirubin concentrations in the immediate neonatal period suggest that cord blood hydrogen peroxide levels can be used to predict severe neonatal indirect hyperbilirubinemia.

Limitation of this study was in the form of small sized sample of the study and difficulty in measurement of hydrogen peroxide (H₂O₂) at the fifth and seventh days of life for controls due to financial aspects.

Conclusion

Cord blood hydrogen peroxide (H₂O₂) levels can be used as an early predictor of neonatal indirect hyperbilirubinemia and can determine which neonates should be followed after discharge from the hospital