The Differences of Urinary Neutrophil Gelatinase-Associated Lipocalin (NGAL) Levels between Asphyxiated and Non-Asphyxiated Neonates ()
1. Introduction
Neonatal asphyxia is still the leading cause of high morbidity and mortality in developed countries, as well as in developing countries including Indonesia. Global estimates for asphyxia-related neonatal deaths vary from 0.7 to 1.2 million, and about 99% of neonatal deaths are due to asphyxia occurred in low- and middle-income countries [1] . Incidence of neonatal asphyxia in Indonesia is about 3% - 5% of all live births [2] .
Asphyxia could reduce renal blood flow and might cause organ dysfunction and tubular renal damage [3] -[6] . Damaged tubular cells will produce and secrete biological substances that related to innate immune response and inflammation process including protein [7] -[9] . Neutrophil gelatinase-associated lipocalin (NGAL) is a protein that is secreted by immune cells, hepatocytes, and renal tubular cells. Neutrophil gelatinase-associated lipocalin could be overly expressed after renal ischemic and it could be detected with higher concentration in urine [10] - [13] .
Neutrophil gelatinase-associated lipocalin has been used as a biomarker for acute kidney injury (AKI) in critically ill neonates and children. From previous studies, Askenazi et al. [14] described urine NGAL levels in very low birth weight newborns which were diagnosed with AKI, and showed elevated urine NGAL levels. Krawc- zeski et al. [15] compared serum and urine NGAL levels in neonates and children after cardiopulmonary bypass (CPB), and showed elevated serum and urine NGAL levels 2 hours after CPB and it can be used for biomarker of AKI. Sarafidis et al. [16] compared serum and urine cystatin-c levels, serum and urine NGAL levels, and urine kidney injury molecule-1 (KIM-1) levels with serum creatinin levels in term asphyxiated and non-asphy- xiated newborn, and showed a significant elevated serum cystatin-c levels, also elevated serum and urine NGAL levels in asphyxiated newborn. Serum and urine NGAL levels elevated in asphyxiated newborn with AKI inspite of non-AKI asphyxiated newborn [14] -[16] .
The aim of this study is to evaluate the differences between urinary NGAL levels in asphyxiated neonates and non-asphyxiated neonates.
2. Materials and Methods
This cross-sectional study was performed in Neonatology Division of Dr. Hasan Sadikin Hospital Bandung, Indonesia from December 2014 to March 2015. Subjects of this study were calculated by unpaired data analysis for two independent groups, and minimum sample size estimation was 17 each group. Seventeen neonates were diagnosed as asphyxia based on 2 from the following American Academy of Pediatrics’ criteria [17] : 1) umbilical cord arterial pH less than 7; 2) Apgar score of 0 to 3 for longer than 5 minutes; 3) neurologic manifestations (eg, seizures, coma, hypotonia); and 4) multisystemic organ dysfunction, and 17 neonates were born without asphyxia. The exclusion criteria were baby born with multiple congenital anomaly and mother with infection risks. This study was approved by the ethical committee of the Faculty of Medicine, Universitas Padjadjaran/Dr. Hasan Sadikin General Hospital Bandung, Indonesia.
Urine samples were collected after informed consent from their parents. Urine NGAL examination was performed with ELISA technique. Data were presented as mean, standard deviation, and median with range. Statistical parameters were calculated using SPSSTM version 20.0. Due to unnormally distributed data, the nonparametric Mann-Whitney U test was used to determine the differences of urinary NGAL levels between the groups. The Fisher’s exact test was used to determine the differences of gestational age and birth weight in both groups. p values < 0.05 were considered as significant.
3. Results
Thirty four babies, who were born in Neonatology Division of Dr. Hasan Sadikin General Hospital in Bandung, Indonesia, consisted of 20 males and 14 females were divided into 17 asphyxiated neonates group and 17 non- asphyxiated neonates group. The clinical characteristics of the subjects are presented in Table 1, while factors which associated with urine NGAL levels are presented in Table 2.
The results from data analysis with Fisher exact test on the differences of gestational age and birth weight between asphyxiated and non-asphyxiated neonates were not significant (Table 2). The differences of urine NGAL levels between asphyxiated and non-asphyxiated neonates were analyzed using Mann-Whitney U test, and they are presented in Table 3.
The median urine NGAL levels in both groups were statistically significant different (p < 0.001).
Table 1. Characteristics of the subjects (n = 34).
SD: standard deviation.
Table 2. Factors associated with urine NGAL levels.
*Fisher’s exact test.
†Mann-Whitney U test.
4. Discussion
Asphyxiated group had gestational age ≤ 36 weeks more than >36 weeks while the mean gestational age was 34 (26 - 40) weeks, and the mean birth weight was 2190 (800 - 3400) gram. Non-asphyxiated group had gestational age >36 weeks more than ≤36 weeks while the mean gestational age was 37 (32 - 42) weeks, and the mean birth weight was 2727 (1500 - 3920) gram. This study is different from previous studies. Sarafidis et al. [16] and El- Salam et al. [18] included term neonates and excluded preterm and very low birth weight neonates.
This study also determined the differences of gestational age and birth weight as factors which were associated with urine NGAL levels between asphyxiated and non-asphyxiated neonates. There were no significant differences in gestational age and birth weight between the groups (p = 0.163; p = 1.0).
The results of this study showed the median urinary NGAL levels in asphyxiated group was 506.7 (60.0 - 651.7) ng/mL, elevated significantly from normal value. The median urinary NGAL levels in non-asphyxiated group was 6.7 (0.1 - 53.0) ng/mL. Statistically, there were significant differences of urinary NGAL levels between asphyxiated and non-asphyxiated group (p < 0.001).
Neonatal asphyxia is a leading cause of renal hypoxia and ischemia. Reduced renal blood flow is a major cause of overly NGAL express in tubular renal [12] . Normally, circulating NGAL is filtered in the glomerulus and reabsorbed by the proximal tubule. Consequently, low levels of NGAL are detected in plasma and urine [12] -[14] . In renal tubular damage, circulating NGAL were not well reabsorbed by proximal tubule and induced synthesis NGAL de novo in distal tubule [11] [19] . Neutrophil gelatinase-associated lipocalin could elevate and could be detected in the higher concentration of urine before progressive renal damage and death cells [12] [20] .
Previous studies with different subject had been conducted beforehand. Sarafidis et al. [16] compared urine NGAL levels between asphyxiated and non-asphyxiated term neonates, and showed that there were significant differences of urinary NGAL levels in both groups (p = 0.006), and urinary NGAL levels showed elevated in asphyxiated neonates with AKI inspite of non-AKI asphyxiated neonates. El-Salam et al. [18] reported urinary NGAL levels in term asphyxiated neonates had a significant elevation in 48 hours after birth and before the rising of creatinin serum levels than in control group (p = 0.01).
Limitation of this study is asphyxia based on AAP’s criteria not to evaluate all of the criteria, but only from the Apgar score and pH in arterial blood gas because we required more time to observe other criteria. We also did not exclude multiple congenital anomaly condition from objective examination, but only from physical examination. NGAL examination was only to evaluate differences in asphyxiated and non-asphyxiated neonates, not including creatinin serum examination and not to observe occurrence of AKI. However, due to our limitations, more studies are required.
5. Conclusion
Urinary NGAL levels in asphyxiated neonates were significantly higher than those in non-asphyxiated neonates. There were significant differences of urine NGAL levels between the groups.
Acknowledgements
Our study was conducted with private funding. We thanked Professor Abdurachman Sukadi and Professor Herry Garna for initial manuscript preparation counseling. NDF, TY, and DR contributed to conception and design of the study, acquisition of data, interpretation and analysis of data, revising the article and final approval of the version submitted. We also thank to the parents for their children’s participation in the present study.
NOTES
*Corresponding author.