PMID- 33861987 OWN - NLM STAT- MEDLINE DCOM- 20210806 LR - 20210806 IS - 1873-2933 (Electronic) IS - 0009-9120 (Linking) VI - 93 DP - 2021 Jul TI - Polymorphisms of interleukin 4 and interleukin 4 receptor genes and bronchial asthma risk among Egyptian children. PG - 66-72 LID - S0009-9120(21)00109-0 [pii] LID - 10.1016/j.clinbiochem.2021.04.006 [doi] AB - BACKGROUND: Interleukin 4 (IL4) is a key cytokine that regulates the inflammatory cascade in bronchial asthma. We investigated the association between the IL4 and IL4R polymorphisms and the susceptibility for bronchial asthma among Egyptian children. METHODS: IL4 VNTR and IL4R c.1902 A>G p.(Q576R) polymorphisms were investigated among 100 children with bronchial asthma and 100 healthy controls using PCR method. Serum levels of IL4 and immunoglobulin E (IgE) were assessed by ELISA. RESULTS: The frequencies of (A1A2 + A2A2) genotypes and A2-allele of the IL4 VNTR variant were significantly higher among asthmatic patients than controls (p = 0.01, OR = 2.34, 95% CI = 1.24-4.44; p = 0.01, OR = 2.27, 95% CI = 1.29-3.99, respectively). The frequencies of (AG + GG) genotypes and G-allele of the IL4R (A1902G) variant were significantly higher among asthmatic patients than controls (p = 0.003, OR = 2.52, 95% CI = 1.39-4.58; p = 0.002, OR = 2.25, 95% CI = 1.35-3.76, respectively). There was a significant association between (A1A2 + A2A2) genotypes of the IL4 VNTR variant and high serum IL4 level among asthmatic patients (p < 0.001). The (AG + GG) genotypes of the IL4R (A1902G) variant were significantly associated with exposure to triggers, atopic dermatitis and higher serum IgE level in asthmatic patients (p = 0.02, 0.04 and 0.01, respectively). CONCLUSION: IL4 VNTR and IL4R (A1902G) polymorphisms could be associated with higher risks of bronchial asthma among Egyptian children. CI - Copyright (c) 2021 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved. FAU - Elsaid, Afaf AU - Elsaid A AD - Biochemistry Section, Mansoura University Children's Hospital, Mansoura, Egypt. FAU - Shoaib, Rasha M S AU - Shoaib RMS AD - Biochemistry Department, Faculty of Science, Damietta University, Damietta, Egypt. Electronic address: rashashoaib83@yahoo.com. FAU - Badr, Sara S AU - Badr SS AD - Biochemistry Department, Faculty of Science, Damietta University, Damietta, Egypt. FAU - Wahba, Yahya AU - Wahba Y AD - Pediatric Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt. FAU - Ayyad, Seif-Eldin N AU - Ayyad SN AD - Chemistry Department, Faculty of Science, Damietta University, Damietta, Egypt. LA - eng PT - Journal Article DEP - 20210420 PL - United States TA - Clin Biochem JT - Clinical biochemistry JID - 0133660 RN - 0 (IL4 protein, human) RN - 0 (IL4R protein, human) RN - 0 (Interleukin-4 Receptor alpha Subunit) RN - 207137-56-2 (Interleukin-4) RN - 37341-29-0 (Immunoglobulin E) SB - IM MH - Alleles MH - Asthma/blood/complications/*genetics/immunology MH - Case-Control Studies MH - Child MH - Dermatitis, Atopic/blood/etiology/genetics/immunology MH - Female MH - Genetic Predisposition to Disease MH - Genotype MH - Healthy Volunteers MH - Humans MH - Immunoglobulin E/blood MH - Interleukin-4/blood/*genetics MH - Interleukin-4 Receptor alpha Subunit/*genetics MH - Male MH - Polymorphism, Single Nucleotide/*genetics MH - Principal Component Analysis OTO - NOTNLM OT - Bronchial asthma OT - Interleukin 4 OT - Interleukin 4 receptor EDAT- 2021/04/17 06:00 MHDA- 2021/08/07 06:00 CRDT- 2021/04/16 20:10 PHST- 2021/02/09 00:00 [received] PHST- 2021/04/01 00:00 [revised] PHST- 2021/04/09 00:00 [accepted] PHST- 2021/04/17 06:00 [pubmed] PHST- 2021/08/07 06:00 [medline] PHST- 2021/04/16 20:10 [entrez] AID - S0009-9120(21)00109-0 [pii] AID - 10.1016/j.clinbiochem.2021.04.006 [doi] PST - ppublish SO - Clin Biochem. 2021 Jul;93:66-72. doi: 10.1016/j.clinbiochem.2021.04.006. Epub 2021 Apr 20.