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Published on: June 21, 2018
ADAM33 genetic polymorphisms and risk of atopic dermatitis among Japanese children
Aya Matsusue1, Chikako Kiyohara, Keiko Tanaka
1Department of Forensic Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, Japan.
Insights
The ADAM33 gene polymorphism rs2853209 is associated with a reduced risk of atopic dermatitis (AD) in Japanese children. This finding suggests a potential genetic link between ADAM33 and AD development.
Area of Science:
- Genetics
- Dermatology
- Immunology
Background:
- ADAM33 is a known asthma susceptibility gene.
- Understanding genetic factors in atopic dermatitis (AD) is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the association between ADAM33 gene single nucleotide polymorphisms (SNPs) and atopic dermatitis (AD) in Japanese children.
- To explore the potential role of ADAM33 in the pathogenesis of AD.
Main Methods:
- A case-control study was conducted with 140 AD cases and 258 controls.
- Seven specific SNPs of the ADAM33 gene were analyzed.
- Genotyping was performed to identify associations between SNPs and AD risk.
Main Results:
- The SNP rs2853209 (T>A) showed a significant association with reduced AD risk.
- Individuals with the AA genotype for rs2853209 had a lower risk of AD (OR=0.55).
- A haplotype containing the rs2853209 A allele was significantly associated with decreased AD risk (OR=0.26).
Conclusions:
- This study provides initial evidence for an association between ADAM33 gene polymorphism and atopic dermatitis risk in Japanese children.
- The findings suggest that specific ADAM33 variants may confer protection against AD.
- Further research with larger sample sizes is needed to confirm these results and elucidate the underlying mechanisms.
Objectives:
ADAM33, a disintegrin and metalloproteinase 33, gene has been identified as an asthma susceptibility gene. The relationship between single nucleotide polymorphisms (SNPs) in ADAM33 and atopic dermatitis (AD) in Japanese children was examined using case-control design.
Methods:
Seven SNPs of ADAM33 (rs2853209, rs2787094, rs2280091, rs2280090, rs628977, rs597980, and rs528557) were analyzed in 140 AD cases and 258 controls aged 3 years.
Results:
Only rs2853209 (T>A) was significantly associated with AD risk. Sex-adjusted odds ratio (OR) for the AA versus the TT genotype was 0.55 (95% confidence interval (CI), 0.30-0.997). Consistent with the results of genotyping analysis, a haplotype carrying rs2853209 A allele was significantly associated with decreased risk of AD compared to all the other haplotypes combined (OR=0.26, 95% CI=0.08-0.69).
Conclusion:
This is the first study to provide evidence for an association of the ADAM33 polymorphism with AD risk but the strength of this evidence is limited by our small sample size.
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