Association between cord blood IgE levels in newborns and family history of atopic diseases
Abstract
Background Cord blood-IgE (CB-IgE) levels have been usedwidely as a specific marker of atopic diseases. In some previous
studies, CB-IgE levels in subjects with and without a family history
of atopic diseases have been controversial.
Objective To determine the CB-IgE level in newborns and to iden-
tify the association between CB-IgE and family history of atopic
diseases.
Methods A cross-sectional study was done to compare the CB-IgE
levels in neonates with or without a family history of atopic diseases
in mother, father, or siblings. Subjects of this study were 124 new-
borns who consecutively born in Puskesmas Kiaracondong,
Bandung, during the period of March 2001 to July 2002. Subjects
were divided into 2 groups based on history of atopic diseases.
Measurements of CB-IgE levels were done by sandwich ELISA
methods. Data were analyzed by c 2 statistics, t test, ANOVA, and
Dunkan’s test.
Results The mean CB-IgE levels in the group with and without a
family history of atopic diseases were 3.2±2.5 IU/ml and 0.5±0.5
IU/ml (P<0.001), respectively. The mean CB-IgE levels in male
and female infants with a family history of atopic diseases were
3.3±2.7 IU/ml and 3.03±2.2 IU/ml (P>0.05), respectively. Based
on the cut-off point (1.3 IU/ml), CB-IgE levels had significant posi-
tive association with a family history of atopic diseases (OR 156,
95%CI 29.61;1104.24). CB-IgE levels in neonates with 1, 2, and 3
atopic family members were 1.67±0.78 IU/ml, 3.76±2.11 IU/ml, and
6.6±2.7 IU/ml, respectively (F=32.603; P<0.001).
Conclusion Most newborns with a family history of atopic dis-
eases showed high levels of CB-IgE, but there were no correlation
with gender. The probability of having atopic diseases increase in
concord with the number of family with atopic diseases
References
DP, Terr AI, Imboden JB, editors. Medical immunol-
ogy. 10th edition. New York: McGraw-Hill Company;
2001. p. 349-69.
2. Koning H, Baert MRM, Orange AP, Savekoul HFJ,
Neijens HJ. Development of immune function, related
to allergic mechanisms, in young children. In: Koning
H, editor. T and B cell activation in childhood allergy.
Roterrdam; 1996. p. 11-30.
3. Yadav M. Maternal factors in atopy. Medical progress.
March 2000:15-22.
4. Kay AB, Mackay IR, Rosen FS. Allergy and allergic
diseases. N Engl J Med 2001;1(344):30-7.
5. Hopkin JM. Genetics of atopy. Pediatr Allergy Immunol
1995;6:139-44.
6. Kjellman NAM, Johansson SGO. IgE and atopic al-
lergy in newborns and infants with a family history of
atopic diseases. Acta Pediatr Scand 1976;65:601-7.
7. Savelkoul HFJ, Neijens HJ. Immune responses during
allergic sensitization and the development of atopy.
Allergy 2000;55:989-97.
8. Jones CA, Holloway JA, Warner JO. Does an atopic
disease start in foetal life?. Allergy 2000;55:2-10.
9. Kjellman NAM, Johansson SGO. IgE and atopic al-
lergy in newborns and infants with a family history of
atopic diseases. Acta Pediatr Scand 1976; 65:601-7.
10. Croner S, Kjellman NIM, Eriksson B, Roth A. IgE
screening in 1701 newborns infants and the develop-
ment of atopic diseases during infancy. Arch Dis Child
1982;57:364-8.
11. Edenharter G, Bergmann RL, Bergmann KE, Wahn V,
Fostr J, Zepp F, et al. Cord blood IgE as risk factor and
predictor for atopic diseases. Clin and exp allergy
1998;28:671-8.
12. Eiriksson TH, Sigurgeisson B, Sigfusson A,
Valdimarsson H. Cord blood IgE levels are influenced
by gestational age but do not predict allergyc mani-
festations in infants. Pediatr Allergy Immunol
1994;5:5-10.
13. Velazquez PSV, Angeles MB. Concentraciones de IgE en
sangre de cordon umbilical y su asociacion con factores
de riesgo atopico. Educ Invest Clin 2000; 1(3):172-6.
14. Atici A, Altintas D, Yuksel B, Evliyaoglu N, Evruke C,
Satar M, et al. Do parental smoking and history of al-
lergy influence cord serum IgE?. Pediatr Allergy Immunol
1995;6:213-5.
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Accepted 2016-10-16
Published 2016-10-18