Authors

1 Government Medical College Srinagar, India.

2 Govt Medical College Jammu, India.

3 Govt Medical College Srinagar, India.

Abstract

Background: Febrile seizures are one of the most common neurological conditions of childhood. It seems that zinc deficiency is associated with increased risk of febrile seizures.
Aim: To estimate the serum Zinc level in children with simple Febrile seizures and to find the correlation between serum zinc level and simple Febrile seizures.
Materials and Methods: The proposed study was a hospital based prospective case control study which included infants and children aged between 6 months to 5 years, at Post Graduate Department of Pediatrics, (SMGS) Hospital, GMC Jammu, northern India. A total of 200 infants and children fulfilling the inclusion criteria were included. Patients were divided into 100(cases) in Group A with simple febrile seizure and 100(controls) in Group B of children with acute febrile illness without seizure. All patients were subjected to detailed history and thorough clinical examination followed by relevant investigations.
Results: Our study had slight male prepondance of 62% in cases and 58% in controls . Mean serum zinc level in cases was 61.53±15.87 ugm/dl and in controls it was 71.90+18.50 ugm/dl .Serum zinc level was found significantly low in cases of simple febrile seizures as compaired to controls ,with p value of

Keywords

Introduction: International league against epilepsy (ILAE) has defined an epileptic seizure as transient occurrence of signs and/or symptoms due to abnormal, excessive or synchronous neuronal activity in the brain. Febrile seizures are seizures that occur between the age of 6 and 60 months with a temperature of 38°C or higher, that are not the result of central nervous system infection or any metabolic imbalance, and that occur in the absence of a history of prior non-febrile seizures (1). Various factors have been described in the pathophysiology of febrile seizures like bacterial and viral infections (2), susceptibility of the immature brain to temperature (3), association with interleukins (4), circulating toxins (5), trace element deficiency (6) and iron deficiency (7). Role of trace elements like Selenium, Magnesium, Copper and Zinc have been described in association with febrile seizures (7).Trace elements appear to play a role by their ability to modulate neurotransmission by acting on ion channels and their coenzyme activity.

Zinc is an important element in growth, development and normal brain function. It is also an important cofactor for different enzymes, is involved in cellular growth and differentiation, enzymatic activity of different organs, proteins and cellular metabolism. In brain, zinc is present in synaptic vesicles in subgroup of glutaminergic neurons. In this form it can be released by electrical stimulation and may serve to modulate responses at receptors level. These include both excitatory and inhibiting receptors particularly NMDA (N-methyl-D aspartate) and GABA (Gamma aminobutyric acid) receptors respectively (8,9).

 

Decreased zinc levels modulates the activity of glutamic acid decarboxylase, the rate limiting enzyme in the synthesis of Gamma Amino Butyric Acid (GABA), which is a major inhibitory neurotransmitter (8). Any abnormalities of GABAergic function, including synthesis, synaptic release, receptor composition, trafficking or binding, and metabolism, can each lead to a hyperexcitable, epileptic state (9,10). Zinc has an inhibitory effect on N-methyl-D-aspartate receptors, which is responsible for excitatory phenomenon after binding with glutamate. Thus decreased Zn levels may play a role in pathogenesis of febrile seizures. Previous studies have reported the low serum Zinc level in children with febrile seizures (11,12,13,14,15). The present study intends to estimate the serum Zinc levels in children with febrile seizure and acute febrile illness without seizure and to correlate the serum Zinc level with simple febrile seizures.

          Materiel and methods: The proposed study was a hospital based prospective case control study with RCT code of AEARCTR-0000631 which included   infants and children aged between 6 months to 5 years, at Post Graduate Department of Pediatrics, Shri Maharaja Gulab Singh (SMGS) Hospital, Jammu. All patients whose parents/guardians have consented for the study and had Simple febrile seizure, normal development, age between 6 months and 5 years were included as cases and patients with with Complex febrile seizure, age younger than 6 months and older than 5 years,  history of recent zinc intake, developmental delay and or neurologic deficit, malnutrition, acute and chronic diarrhea, electrolyte imbalance were excluded from the study. The axillary temperature was recorded in all children with mercury thermometer placed in axilla for three minutes, followed by general examination and systemic examination in detail.

Taking all aseptic precautions, 2 ml of blood from venipuncture using 22 gauge sterile needle, within 24 hours of contact of patient in both the groups. The sample was centrifuged for 3-4 minutes at 3000-4000 rpm, serum thus obtain and preserved in sterile deionized vial. Estimation of serum zinc was done within 6 hours of collection. Method used was based on colorimetric test kit, reagent used was 2-(5-bromo-2-pyridylazo)-5-(N-propyl-N-sulphopropylamino)-phenol. Zinc forms a red chelate with it. Increase in the absorbance of wavelength 560 nm can be measured and is proportional to concentration of the zinc.

        Statistical analysis: Data was analyzed using MS Excel SPSS version 17.0 for windows. zinc level  presented as mean and standard deviation, the difference in mean among the groups was assessed by use of 1 way ANOVA followed by post hoc bonferronis t test to analyze inter group difference. Correlation was analyzed with relevant statistical method. Correlation co-efficient was calculated. A p value less than 0.05 was taken as statistically significant.

Results:

Table 1: Age  group  distribution of Group A & Group B

Age Group(months)

Group A(cases) =100

Group B (controls) =100

No

%

No

%

6-12

36

36%

28

28%

13-24

35

35%

39

39%

25-36

15

15%

23

23%

37-48

8

8%

5

5%

49-60

6

6%

5

5%

           

Table 1 represents the mean age of Group A and Group B. Mean age was  nearly similar in both the Groups.

Table 2: Gender distribution of Group A & Group B

 

Sex

Group A (cases)   n=100

Group B (controls)  n=100

No

%

No

%

Male

62

62%

58

58%

Female

38

38%

42

42%

   p=0.683

Table 2 represents the gender distribution of population of and shows that Males predominated in both the groups.

 

 

 

Table 3:  Distribution of diagnosis in Group A and Group B

Daignosis

Group A (cases)

Group B (controls)

No.

%

No.

%

ARI

20

20

42

42

NON LOCALISED FEVER (viral)

60

60

46

46

UTI

5

5

4

4

ASOM

10

10

5

5

BRONCHIOLITIS

5

5

3

3

Total

100

100

100

100

Table 3 represents the distribution of diagnosis  in Group A and Group B and shows that non localized fever(viral) predominated as the cause of fever in both the Groups, followed by ARI and ASOM.

 

 

Table 4:        Comparison of mean serum Zinc level between Group A         and Group B.

       Variables

Serum Zinc
level
(ugm/dl)

Mean
difference

p-value

Group A

61.53±15.87

-10.45

<0.05

Group B

71.90+18.50

 P<0.005

 Table 4 represents the mean serums zinc level in both the Groups. Mean serum zinc level was 10.45 ugm/dl less in cases of simple febrile seizure as compared to controls. 

Table 5:       Comparison of Zinc deficiency among Group A and     Group B

Zinc level

Group A

Group B

Total

No.

%

No.

%

No.

%

 

60

60

34

34

94

47

>65 µgm/dI

40

40

66

66

106

53

Total

100

 

100

 

200

 

  P=.001

Table 5 represents the number of patients in both Groups with bio-chemical hypozincemia and shows that 60% of the cases and 34% of the controls had bio-chemical hypozincemia. 

        DISCUSSION: Zinc is an essential micronutrient required for the normal function and development of the central nervous system. It has a role in modulation of neurotransmission by inhibitory effect on the Glutaminergic NMDA receptor, and by acting as a cofactor to the rate limiting enzyme in GABA synthesis. Hence its deficiency can lead to the excitation inhibition imbalance precipitating a febrile seizure.

Few  authors have studied the relationship between serum zinc level and simple febrile seizures, majority of which support  the association of hypozincemia with simple febrile sizures, on the contrary few do not.  The present study was under taken in this context to study the correlation of serum zinc level with simple Febrile seizures.

More than two third of the patients were below 2 years with mean age of 22.72 and 25.67 months in cases and controls respectively.

 Mean age in cases falls within the range of mean age of (21-27 months) as reported by others (12, 16; 17, 18, 19, 20). Males predominated in present study with male female ratio of 1.63:1.This was similar to the gender ratio ranging from 1.4-1.7:1 as reported by ( 6,11,12, 16 17, 18,20).  Family history of seizures was present in 9%, 6% had history of simple febrile seizures in the first degree relatives and 3% had history of epilepsy in family).while among 3% patient with family history of epilepsy 2% had history in first degree and 1% had history in second degree relative. Similar findings were reported by (21) who reported family history in 10% of patients. However (7,12,19,) reported family history in 44.4%, 48%, 26% of patients respectively. The clinical presentation comprised of mainly non localized fevers majority of which had clinical evidence to suggest viral etiology (60%), followed by ARI (20%), ASOM (10%), UTI (5%) and Bronchiolitis (5%). (12,22) have  reported ARI as most common cause and Ehsanipouri et al, 2009 reported viral infections as a predominant  cause of fever in their study. Majority of the authors who have correlated serum zinc level with  simple febrile seizure have studied this correlation by compairing mean serum zinc level between cases and controls, while few others studied this correlation by determining the number  of patients having hypozincemia in subject population. Data was analyzed in the present study by both these methods. As per WHO recommendation the cut off value for hypozincemia has been taken as 65µgm/dl. (23).Hence 65µgm/dl was taken as cutoff for hypozincemia as suggested by WHO. Hypozincemia was present in  majority of the patients (60% ), though no statistical significant difference was found in the mean age, gender distribution, physical parameters, and nutritional status between the patients of hypozincemia and normal zinc level. Similar findings were reported by (18).

Mean serum zinc levels obtained in various studies.

Studies

  Serum Zinc level(µgm/dl)

  Mean Difference

  p-value

   cases

       control

 

Ganesh R et al.(16)

    32.17

87.60

  55.43

 <0.001**

Okposio et al. (24)

    58.70

90.30

  31.6

 <0.001**

  Mahyar et al.(18)

    62.84

           85.7

  22.86

 <0.05*

Burhangnoglu(25). 181

    66.00

98.00

  32

 <0.05*

  Amiri et al.(6)

    66.13

          107.8

  41.67

 <0.05*

Heydarian F (17)

    66.37

75.83

  9.46

 <0.001**

  Ehsani et al(11)

    76.80

           90.12

  13.32

 < 0.05*

Margaretha(12)

    88.30

       137.20

  48.9

 <0.001**

Modarresi etal.(26)

    93.39

130.54

  37.15

 <0.001**

Kafadar  et al.(19)

    110.49

   107.12

   -3.37

 0.673

Talebian et al.(20)

  116.28

           146

 29.72

<0.05*

Present Study

   61.53

71.99

  10.46

<0.05*

           

*significant

**highly significant

 

 In the present study significant difference of 10.46µgm/dl was obtained in mean serum zinc level in cases as compared to controls. Similar findings have been reported by (6,11,12,13,14,15,16,17,18,20,25)as shown in table above. The present study also did not reveal any significant difference in mean serum zinc level in relation to age groups or gender. Similar findings were reported by (16,19,20 and 25), Thus the present study reveals that no specific age group or gender is particularly predisposed to develop  hypozincemia.

Hypozincemia was observed to be more frequent in children with simple febrile seizures in the present study. Clinical presentation of those patients with biochemical hypozincemia did not differ from those with normal zinc levels. No classical clinical manifestations of hypozincemia as mentioned in literature like diarroea, impaired appetite, decreased growth velocity, acro orificial skin lesions, delayed wound healing, dysgusia and hypogusia were present in the patients of hypozincemia. Neither these patients had any predisposing conditions associated with hypozincemia like Acrodermatitis enteropathica, recent gastrointestinal tract infection, malabsorption, chronic liver disease or chronic illness. Hence most of these patients had purely biochemical hypozincemia. Thus it appears that presence of hypozincemia in presence of other risk factors of   febrile seizures may enhance the occurrence of febrile seizures explaining a possible correlation between low serum zinc levels and simple febrile seizures. However, large randomized control trials are recommended to analyze this association and if proven, the possibility of prophylactic zinc supplementation in reducing the risk of febrile seizures in such patients.

Acknowledgment: The authors want to thank the parents and the guardians  who consented for the participation of their children in the  study.

Conflict of interest: None.

 
 1.                  American Academy of Pediatrics. American Academy of' Pediatrics: Steering Committee on Quality Improvement and Management, Subcommittee on Febrile Seizures. Febrile Seizures: clinical practice guideline for the long-term management of the child with simple febrile seizures. Pediatrics 2008;121:1281-6.
2.                  Millichap JG, Millichap JJ. Role of viral infections in the etiology of febrile seizures. Pediatr Neurol 2006 ;35(3): 165-72.
3.                  Holtzman ft Obana K, Olson J. Hyperthermia- induced seizures in the rat pup: a model for febrile convulsions in children. Science 1981;213:1034-6.
4.                    Tsai FJ, Hsieh YY, Chang CC. Polymorphisms for interleukin I beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions. Arch Pediatr Adolesc Med 2002; 156:545-8.
5.    
Virta M. Hurme M, Helminen M. Increased plasma levels of pro- and anti-inflammatory cytokines in patients with febrile seizures. Epilepsia 2002;43:920-3.
6.                  Amiri M, Farzin L, Moassesi ME, Sajadi F. Serum Trace Element Levels in Febrile Convulsion. Biol Tr Elem Res 2010;135(1):38-44.
7.                  Kumari PL, Nair MK, Nair SM, Kailas L, Geetha S. Iron deficiency as a risk factor !br simple febrile seizures - a case control study. Indian Pediatr 2011; 49:17-9.
8.                  Ebadi M, Wilt 5, Ramaley R. The role of Zinc and Zinc-binding proteins in regulation of glutamic acid decarboxylase in brain. Chemical and biological aspects of vitamin B6, Catalysis. New York: Alan R Liss; 1984;255-275.
9.                  Cossart R, Bernard C, Ben-Ari Y. Multiple facets of GABAergic neurons and synapses: multiple fates of GABA signalling in epilepsies. Trends Neurosci 2005;28:108-15.
10.              Macdonald RL, Kang JQ. Molecular pathology of genetic epilepsies associated with GABAA receptor subunit mutations. Epilepsy Curr 2009; 9:18-23.
11.              Ehsani F, Vahid-Harandi M, Kany K. Determination of serum Zinc in children affected by febrile convulsion and comparison with control group. The Journal of Iranian Medical Sciences University 2006; 12:219-76.
12.         Margaretha L, Masloman N. Correlation between serum Zinc level and simple febrile seizure in children. Pediatr Indones 2010;50(6):326-30.
13.          Iman Abd El Rehim  Mohamed Aly, Howyda Mohamed Kmal,  Doaa Refaey Soliman and Mona Hassan Mohamed. Iron profile parameters and serum zinc & copper levels in children with febrile convulsions in Banha. Journal of American Science 2014;10(7)
14.         Srinivasa , Manjunath. Serum zinc levels in children with simple seizures..Journal of evolution  of medical and dental sciences 2014
15.         Siddarth S. Joshi and Sumanth Shetty.  Zinc levels in Febrile Seizures. International Journal of Biomedical Research 2014
 16.              Ganesh R, Janakiraman L. Serum Zinc levels in children with simple febrile seizure. Clin Pediatr (Phila) 2008;47:164-6.
17.              Heydarian F, Ashrafzadeh F, Ghasemian A. Serum Zinc level in patients with simple febrile seizure. Iran J Child Neurology 2010;4(2):41-4.
18.              Mahyar A, Pahlavan A, Varasteh-Nijad A. Serum Zinc level in children with febrile seizure. Acta Medica Iranica 2008;46(6):67-9.
19.              Kafadar I. Akini AB. Pekun F. Ada E. The Role of Serum Zinc Level in Febrile Convulsion Etiology. J Pediatr 1nf 2012;6:90-3.
20.              Talebian A, Vakili Z. Talar SA, Kazerni M. Mousavi GA. Assessment of the relation between serum Zinc and magnesium levels in children with febrile convulsion. Iranian Journal of Pathology 2009;4:157-60.
21.              Guzman AR, Castillejos EL, Vicuña WL, Laguia VL, Balarezo W. Gurreoner RL. Anemia: a possible risk factor for the first febrile seizure. Paediatrica 2005;7(2):62-5.
22.              Günduz Z, Yavuz I, Koparal M, Kurnanda S. Saraymen R. Serum and cerebrospinal fluid Zinc levels in children with febrile convulsions. Acta Paediatr Jpn 1996;3
23.              World Health Organization and United Nations Children Fund. Clinical management of acute diarrhoea. WHO/UNICEF Joint Statement; 2004. 8(3):237-41
24.              Okposio Matthias M, Wilson Sadoh, Gabriel Ofovwe, Alphonsus Onyiriuka. Serum Zinc level in Nigerian children with febrile convulsion. Journal of Pediatric Neurology 2012;10 (3).
25.                               Barhanoglu M, Tutuncuoglu 5, Coker C, Tekgul H, Ozgur T. HypoZincaemia in febrile convulsion. Eur J Pediatr 1996;155(6):498-501.
26.         Modarresi MR, Shahkarami SMA, Yaghini 0, Shahbi J, Mosaiiebi D, Mahmoodian T. The relationship between Zinc deficiency and Febrile seizures.