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Published on: June 21, 2018
Association of ADAM33 gene polymorphisms with asthma in Indian children
Shally Awasthi1, Priya Tripathi, Subramaniam Ganesh
1Department of Pediatrics, Chhatrapati Shahuji Maharaj Medical University, Lucknow, India. shallya@rediffmail.com
Insights
Genetic variations in the ADAM33 gene are linked to childhood asthma risk in Indian children. Specific single-nucleotide polymorphisms (SNPs) and haplotypes significantly influence susceptibility to this common respiratory condition.
Area of Science:
- Genetics
- Pediatrics
- Respiratory Medicine
Background:
- Asthma is a prevalent chronic childhood respiratory disorder.
- Asthma exacerbations contribute significantly to childhood morbidity and hospitalizations.
- Understanding genetic factors influencing asthma susceptibility is crucial for early intervention.
Purpose of the Study:
- To investigate the association between ADAM33 gene single-nucleotide polymorphisms (SNPs) and asthma in Indian children.
- To identify specific SNPs and haplotypes of the ADAM33 gene that confer risk or protection against childhood asthma.
- To analyze the genetic susceptibility to asthma in a pediatric population from India.
Main Methods:
- A case-control study design was employed.
- Genotyping of five ADAM33 gene SNPs (F+1, S2, ST+4, ST+5, V4) was performed using PCR-restriction fragment length polymorphism.
- Statistical analyses included the chi-squared test, logistic regression, and haplotype analysis using the expectation-maximization algorithm.
Main Results:
- Significant associations were found between SNPs S2 and ST+5 and asthma risk.
- Homozygous mutant genotypes and mutant alleles of F+1, ST+4, and V4 SNPs were associated with increased asthma risk.
- Specific haplotypes (AGCCT, GGACT, AGCCC) showed a positive association with asthma, while others (ACAGT, AGCGC, AGCGT, GCAGC, GCCGT) exhibited a protective effect.
Conclusions:
- Polymorphisms in the ADAM33 gene are associated with susceptibility to childhood asthma in the Indian population.
- Certain ADAM33 gene variants may modify an individual's risk of developing asthma.
- These findings contribute to understanding the genetic basis of asthma in children.
Abstract:
Asthma is the most common chronic disorder in childhood, and asthma exacerbation is an important cause of childhood morbidity and hospitalization. In the present study, the relationship between single-nucleotide polymorphisms (SNPs) of the ADAM33 gene and asthma in Indian children has been examined using a case-control study. Five SNPs of the ADAM33 gene, F+1(rs511898) G/A, S2 (rs528557) G/C, ST+4 (rs44707) A/C, ST+5 (rs597980) C/T and V4 (rs2787094) C/G, were analyzed in 211 asthma cases and 137 controls aged 1-15 years using the PCR-restriction fragment length polymorphism method. Data were statistically analyzed using the χ(2)-test and logistic regression model. Haplotype estimation and linkage disequilibrium were conducted using the expectation-maximization algorithm. The genotypes and allele frequencies of SNPs S2 and ST+5 of the ADAM33 gene were significantly associated with asthma risk (P = 0.020 - < 0.001), whereas F+1, ST+4, V4 homozygous mutant genotypes and mutant alleles were significantly associated with increased asthma risk (P = 0.031 - < 0.001). A positive association was also found with haplotypes AGCCT, GGACT and AGCCC (P = < 0.001, odds ratio (OR) = 6.10-6.50), whereas ACAGT, AGCGC, AGCGT, GCAGC and GCCGT showed protective association with asthma (P = 0.019-0.000, OR = 0.50-0.20). Taken together, out results suggest that ADAM33 gene polymorphisms may modify individual susceptibility to develop childhood asthma in the Indian population.
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