Comparison of Serum Zinc Level Between Neonates With Jaundice and Healthy Neonates


Hassan Boskabadi 1 , Gholamali Maamouri 1 , Hossein Mohsen Zadeh 1 , Mohammad-Taghi Shakeri 2 , Majid Ghayour-Mobarhan 3 , * , Shabnam Mohammadi 4 , 5 , Gordon AA Ferns 6

1 Department of Pediatrics, Mashhad University of Medical Sciences, Mashhad, IR Iran

2 Community Medicine and Public Health, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IR Iran

3 Biochemistry and Nutrition Research Center and Cardiovascular Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IR Iran

4 Department of Basic Sciences, Faculty of Medicine, Gonabad University of Medical Sciences, Gonabad, IR Iran

5 Neurogenic Inflammation Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, IR Iran

6 Institute for Science and Technology in Medicine, Faculty of Health, University of Keele, Staffordshire, UK

How to Cite: Boskabadi H, Maamouri G, Mohsen Zadeh H, Shakeri M, Ghayour-Mobarhan M, et al. Comparison of Serum Zinc Level Between Neonates With Jaundice and Healthy Neonates, Shiraz E-Med J. 2015 ; 16(11-12):e59924. doi: 10.17795/semj27392.


Shiraz E-Medical Journal: 16 (11-12); e59924
Published Online: December 24, 2015
Article Type: Research Article
Received: January 26, 2015
Revised: April 19, 2015
Accepted: May 27, 2015


Background: Neonatal jaundice is the most common cause of hospitalization in the first month of life. Factors that reportedly affect the severity of neonatal jaundice include: maternal, prenatal and neonatal factors as well as environmental factors (such as zinc). Animal study demonstrated a decrease in serum bilirubin level after zinc treatment in hyperbilirubinemic rats.

Objectives: The current study aimed to investigate serum zinc level in the neonates with idiopatic jaundice.

Patients and Methods: A case-control study was undertaken from 2008 to 2010 on 263 neonates in a neonatal intensive care unit and obstetrics department in Ghaem hospital, Mashhad, Iran. Of the 263 infants, 114 and 149 neonates were in the control and the case groups, respectively. Infants with a gestational age of > 35 weeks or with idiopathic jaundice were included in the study. Exclusion criteria were as follows: neonates with sepsis or any congenital abnormalities or with glucose-6-phosphate dehydrogenase (G-6PD) deficiency, ABO and RH incompatibility. Serum levels of zinc and bilirubin were compared between the control (114 neonates without jaundice) and case (149 neonates with jaundice) groups using atomic absorption spectrometry. The maternal and neonatal information were recorded. Spearman correlation coefficient, chi-square and Mann-Whitney tests were employed to analyze the data by SPSS software.

Results: The mean value of the zinc serum level was 1024.74 ± 245.17 μmol/L in the control group and 841.42 ± 211.99 μmol/L in the case group (P < 0.001). There was no significant correlation between zinc level and factors such as maternal age, multi parity, mode of delivery, hospitalization and gender of infants (P > 0.05). Also, no significant correlation was observed between serum levels of Na, blood urea nitrogen (BUN), creatinine (Cr), white blood cell (WBC), platelet, hematocrit (Hct) and zinc (P > 0.05).

Conclusions: The level of serum zinc in the neonates with hyperbilirubinemia jaundice was lower than that of the ones without jaundice. It seems that zinc has a protective effect. However, more studies are needed for better decision making.

1. Background

Jaundice is the most common reason for admission during the 1st month of life. Multiple variables (maternal, infantile, during labor and environmental factors) affect the course and severity of jaundice (1). Although there may be a benefit to patients with mild hyperbilirubinemia, the subjects with high elevation of serum bilirubin are endangered due to accumulation of bilirubin in the brain tissue (1, 2). Enhanced enterohepatic circulation of bilirubin (EHC) that can occur with resection or bypass in adults or ileal inflammation leads to hypersecretion of bilirubin into the bile with increased formation of black pigment gall stones (3, 4). Since active transport for non-conjugated bilirubin is not proved in the intestine, bilirubin may cycle only via passive diffusion under certain conditions (3-5). Interestingly, two thirds of bilirubin enter the systemic circulation; the remainder reabsorbed from the intestine is removed from blood by the liver (3-7). The final product of heme protein catabolism is an unconjugated bilirubin produced in the reticuloendothelial cells after a chain of enzymatic reactions by the oxygenase, reductase and non-enzymatic reducing agents. Conjugated bilirubin pigments can also be partly due to the deposition of the final product conjugations in hepatocyte by the enzyme bilirubin UDP-glucuronosyl transferase to form a polar water-soluble bilirubin glucuronide (8). One of the factors that affect the severity and incidence of jaundice is the level of serum zinc.

Physiopathology of idiopathic jaundice is unknown in the neonates. Animal studies show that oral administration of zinc decreases serum bilirubin level in the rats. Mendez-Sanchez et al. showed that zinc salts can deposit unconjugated bilirubin and that zinc sulfate suppressed enterohepatic circulation of bilirubin in hamsters (8). Consistent with the study by Vreman et al. who reported that zinc is an inhibitor of heme oxygenase enzyme in both in vitro and in vivo. Administration of zinc (4 μumol/kg) decreased carbon monoxide (CO) and bilirubin levels significantly one to six hours after treatment (9). Zinc salts and other elements such as strontium inhibit the hem-oxygenase enzymes and as a result may prevent jaundice (10).

2. Objectives

The current study aimed to compare the serum zinc level between the healthy neonates and infants with jaundice.

3. Patients and Methods

After the approval of the study by the Ethical committee of Mashhad University of Medical Sciences, parental consent was obtained for each infant. A case-control study was performed from April 2008 to October 2010 in the neonatal intensive care unit (NICU) and obstetrics department, Ghaem hospital, Mashhad, Iran.

Infants with jaundice were treated and formed the case group. Neonates without jaundice formed the control group. Also, the level of zinc serum, severity of jaundice, the type and duration of treatment of the referred infants with jaundice were recorded.

A total of 263 neonates completed the study. Healthy infants with idiopathic jaundice and gestational age >35 weeks were included. Neonates with sepsis, any congenital abnormalities or with ABO blood group system, RH incompatibility; or glucose-6-phosphate dehydrogenase (G-6PD) deficiency were excluded from the study.

To evaluate the serum zinc level, 2 mL of umbilical cord blood were collected and transferred into sterile tubes. All sterile tubes were rinsed with deionized water and acids to be free of trace elements. The blood samples were centrifuged at 1000 rpm and stored at −70°C for future analysis.

Neonates were evaluated for incidence of jaundice in days two, five and seven after birth. Serum levels of zinc and bilirubin were assessed for 114 neonates without jaundice (control group) and 149 neonates with jaundice (case group) using atomic absorption spectrometry. In addition, the amount of jaundice, and duration and type of treatment were recorded in neonates with jaundice. To evaluate jaundice causes, Coombs test (direct and indirect), PBS, Retice count, direct and indirect bilirubin, cell blood count, blood hematocrit and platelet counts were determined in the case group.

3.1. Statistical Analysis

Spearman correlation coefficient, chi-square and Mann-Whitney tests were employed to analyze the obtained data by SPSS software. The data were assessed for normality using the Kolmogorov-Smirnov test. P values less than 0.05 were considered significant.

4. Results

In the current study, 263 neonates were recruited [case group (n = 149) and control group (n = 114)] Table 1. Mean value of serum zinc level was 928.81 ± 247.61 μmol/L in all neonates. Mean of zinc level in the control and case groups were 1024.74 ± 245.17, and 841.42 ± 211.99 μmol/L respectively (P < 0.001) (Figure 1). There was a positive correlation between the level of bilirubin and hospitalization (Table 1, P < 0.001, r = 0.356). Thirty-eight of the subjects were excluded due to failure to follow up, the wrong phone number (16 infants), inaccessibility (12 infants) and physiologic hyperbilirubinemia (10 infants).

Table 1. Characteristics of Mothers and Neonates in the Two Groups
Case Group (n = 149)Control Group (n = 114)P Value
Maternal age, y a27.75 ± 5.5926.52 ± 5.250.071
Multi parity, %49640.009
Age of neonate, d a3.40 ± 1.616.75 ± 4.88< 0.001
Hospitalization, d a2.42 ± 1.512.02 ± 0.770.014
Mode of delivery0.053
History of a child with jaundice0.075

aValues are presented as mean ± SD.

Figure 1. Mean and Range of Changes of Zinc Level in the Case and Control Groups

There was no association between the age of neonates and serum zinc levels between the two groups (P = 0.47) Figure 2. The means of maternal age were 26.52 ± 5.25 and 27.75 ± 5.59 in the control and case groups, respectively. No significant correlation was found between serum level of zinc and maternal age (P = 0.30).

Figure 2. Relationship Between the Age of Neonates and Zinc Level

The rates of multi parity were 64% and 49% between mothers in the control and case groups, respectively. There was no correlation between multi parity and serum zinc levels between the two groups (P = 0.90).

In the control group, 35% of infants were delivered by caesarian and 65% of them were delivered vaginally. In the case group 47% of mothers had caesarian delivery whereas 53% of them had a vaginal delivery (P = 0.05) Table 1. The mean value of the serum zinc level was 897.92 ± 230 in the neonates delivered by caesarian and this value was 953.72 ± 255.93 in the neonates delivered vaginally. There was no significant correlation between the mode of delivery and level of serum zinc in the neonates (P = 0.08). There was a significant correlation between neonatal age and jaundice (3.40 ± 1.61 in the control group versus 6.75 ± 4.88 days in the case group) (P = 0.001, Table 1).

In the control group 50% of infants were boys and 50% girl whereas in the case group 56% of neonates were boy and 44% girl (P = 0.34, Table 1). No significant correlation was observed between serum zinc level and gender of the neonates (P = 0.51, Table 2).

Table 2. Relationship Between Serum Zinc Concentrations (umol/L) and Factors of Neonates and Mothers in the Case and Control Groups
FactorsControl Group aP ValueCase Group aP Value
Having another child with jaundice0.7600.189
Yes1027.00 ± 156.32915.79 ± 312.64
No1054.23 ± 261.79826.79 ± 184.28
Mode of delivery0.5130.338
Caesarian1024.21 ± 270.84824.09 ± 178.57
Vaginal1056.72 ± 233.64858.65 ± 239.46
Male1031.60 ± 114.83835.36 ± 215.80
Female1051.83 ± 294.73846.37 ± 214.28

aValues are presented as mean ± SD.

Table 3. Mean and Range of Changes of the Zinc Level Based on the Incidence of Jaundice
Age of Incidence of JaundiceMean of Zinc umol/LaRange, Minimum - Maximum
Two days207.86 ± 845.16550 - 1910
Three days202.12 ± 820.40502 - 1813
Four days and more237.49 ± 911.31622 - 1480
Total211.14 ± 845.99502 - 1910

aValues are presented as mean ± SD.

No significant correlation was found between possessing a child with jaundice and level of serum zinc (P = 0.63). There was a positive correlation between the levels of direct bilirubin and serum zinc (P = 0.72). Similar results were observed for the correlation between zinc level and hospitalization (P = 0.53). Also, there was no significant relationship among serum levels of Na, blood urea nitrogen (BUN), creatinine (Cr), white blood cell (WBC), platelet, hematocrit (Hct) and serum zinc level (P > 0.05).

Based on statistical results of Kolmogorov-Smirnov test, distribution of serum zinc levels in the control group was normal (P = 0.40) but it was not normal in the case group (P = 0.006). Mean value of serum zinc level was 928.81 ± 247.61 μmol/L in all neonates. The means of zinc level in the control and case groups were 1024.74 ± 245.17, and 841.42 ± 211.99 μmol/L, respectively (P < 0.001) (Figure 2). Q-variance analysis showed that the difference of zinc level was not because of older age of the subjects in the case group and that age was not a interventional factor in the level of zinc serum and this difference could be due to jaundice (P = 0.47).

5. Discussion

The current study results demonstrated that the serum zinc level of the neonates with jaundice was lower than that of the ones without jaundice. Zinc deficiency in pregnant women causes numerous complications for the fetus during pregnancy, such as structural malformations, intrauterine growth retardation (IUGR), premature birth, and SGA in different animal species and human. It is estimated that approximately 50% of women of childbearing age suffer from zinc deficiency. Studies found a relationship among low maternal serum zinc levels, low transferred zinc to the fetus and increase risk of developmental defects. Zinc plays both the structural and enzymatic roles in many proteins. A part of teratogenic effects of zinc deficiency can be due to the changes in the activity of proteins in the embryo (11).

The level of serum zinc increases in the embryo during the third trimester and this accumulation can be especially in the fetal liver. Increased level of fetal metallothionein is also observed. The cause of these changes is still unclear. It may be useful administration of zinc during pregnancy for growth and maturation of the immune system. Congenital abnormalities could result from zinc deficiency (12). There was a significant relationship between maternal serum zinc levels and the incidence of low birth weight (13).

The current study findings showed no correlation between modes of delivery and neonatal zinc level. Past studies show that epidural or spinal anesthesia before cesarean has fewer side effects than other methods. However, general anesthesia is considered as a risk factor for jaundice (14). Based on the findings of another study, there is no relationship between the type of delivery and the severity of jaundice in newborns (15). No relationship was observed between the gender of infants and serum zinc levels. In another study correlation was observed between the level of the neonatal serum zinc and infants’ gender (2010). No association was found between the level of serum bilirubin and zinc in neonates with jaundice. In addition, there was no relationship between serum level of direct bilirubin and zinc. Previous findings showed an inverse relationship between the levels of unconjugated bilirubin and serum zinc (16). The major limitation of the current study was the sampling time in babies with icterus that was three days earlier than those without it. Another limitation was difficulty to follow up neonates and inaccessibility of neonates. The serum zinc level of infants with jaundice was lower than those of the healthy ones. It seems that zinc may have a protective effect in the incidence of neonatal jaundice. However, more evaluations are needed for better decision making.




  • 1.

    Boskabadi H, Maamouri G, Mafinejad S. The Effect of Traditional Remedies (Camel's Thorn, Flixweed and Sugar Water) on Idiopathic Neonatal Jaundice. Iran J Pediatr. 2011; 21(3) : 325 -30 [PubMed]

  • 2.

    Ostrow JD, Pascolo L, Shapiro SM, Tiribelli C. New concepts in bilirubin encephalopathy. Eur J Clin Invest. 2003; 33(11) : 988 -97 [PubMed]

  • 3.

    Brink MA, Slors JF, Keulemans YC, Mok KS, De Waart DR, Carey MC, et al. Enterohepatic cycling of bilirubin: a putative mechanism for pigment gallstone formation in ileal Crohn's disease. Gastroenterology. 1999; 116(6) : 1420 -7 [PubMed]

  • 4.

    Vitek L, Carey MC. Enterohepatic cycling of bilirubin as a cause of 'black' pigment gallstones in adult life. Eur J Clin Invest. 2003; 33(9) : 799 -810 [PubMed]

  • 5.

    Vitek L, Kotal P, Jirsa M, Malina J, Cerna M, Chmelar D, et al. Intestinal colonization leading to fecal urobilinoid excretion may play a role in the pathogenesis of neonatal jaundice. J Pediatr Gastroenterol Nutr. 2000; 30(3) : 294 -8 [PubMed]

  • 6.

    Bloomer JR, Zaccaria J. Effect of graded bilirubin loads on bilirubin transport by perfused rat liver. Am J Physiol. 1976; 230(3) : 736 -42 [PubMed]

  • 7.

    Gartner U, Goeser T, Wolkoff AW. Effect of fasting on the uptake of bilirubin and sulfobromophthalein by the isolated perfused rat liver. Gastroenterology. 1997; 113(5) : 1707 -13 [PubMed]

  • 8.

    Mendez-Sanchez N, Martinez M, Gonzalez V, Roldan-Valadez E, Flores MA, Uribe M. Zinc sulfate inhibits the enterohepatic cycling of unconjugated bilirubin in subjects with Gilbert's syndrome. Ann Hepatol. 2002; 1(1) : 40 -3 [PubMed]

  • 9.

    Vreman HJ, Lee OK, Stevenson DK. In vitro and in vivo characteristics of a heme oxygenase inhibitor: ZnBG. Am J Med Sci. 1991; 302(6) : 335 -41 [PubMed]

  • 10.

    Rodgers PA, Stevenson DK. Developmental biology of heme oxygenase. Clin Perinatol. 1990; 17(2) : 275 -91 [PubMed]

  • 11.

    Hanna LA, Clegg MS, Ellis-Hutchings RG, Niles BJ, Keen CL. The influence of gestational zinc deficiency on the fetal insulin-like growth factor axis in the rat. Exp Biol Med (Maywood). 2010; 235(2) : 206 -14 [DOI][PubMed]

  • 12.

    Lindsay Y, Duthie LM, McArdle HJ. Zinc levels in the rat fetal liver are not determined by transport across the placental microvillar membrane or the fetal liver plasma membrane. Biol Reprod. 1994; 51(3) : 358 -65 [PubMed]

  • 13.

    Boskabadi H, Mamouri G, Nori M, Ayatollahi H, Ghayour-Mobarhan M. The Relationship of Level of Maternal Serum Copper and Zinc with Neonatal Birth Weight. Med J Mashad Univ Med Sci. 2010; 4(52) : 155

  • 14.

    Demiraran Y, Albayrak M, Seker IS, Kaynak G, Iskender A, Sezen GY, et al. Effect of anesthesiological strategies on neonatal bilirubin levels during cesarean section: a prospective and randomized trial. Arch Gynecol Obstet. 2011; 284(5) : 1059 -65 [DOI][PubMed]

  • 15.

    Boskabadi H, Navaei M. Relationship between delivery type and jaundice severity among newborns referred to Ghaem Hospital within a 6-year period in Mashhad. J Obstetr Gynecol. 2011; 14(4) : 15 -21

  • 16.

    Kliegman RM, Jenson HB, Behrman RE, Stanton BF. Nelson textbook of pediatrics. 2007; : 756 -65

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