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Association between CC10 +38A/G polymorphism and asthma risk: A meta-analysis
Guangri Zhao1, Xiaodan Lin2, Ming Zhou3
1Guangri Zhao, Department of Chest Surgery, Department of Chest Surgery, Guangzhou Medical University Cancer Institute and Hospital, Guangzhou, China.
This meta-analysis indicates that the Clara cell 10-kDa protein (CC10) +38A/G polymorphism is associated with an increased risk of asthma. The findings highlight a potential genetic factor contributing to asthma susceptibility.
Area of Science:
- Genetics
- Pulmonology
- Epidemiology
Background:
- Inconsistent results exist regarding the association between Clara cell 10-kDa protein (CC10) +38A/G polymorphism and asthma susceptibility.
- Previous studies have yielded inconclusive findings on this genetic link.
Purpose of the Study:
- To conduct a meta-analysis assessing the association between CC10 +38A/G polymorphism and asthma risk.
- To consolidate existing evidence and provide a more definitive conclusion on the genetic predisposition to asthma.
Main Methods:
- A systematic literature search identified relevant case-control studies published between January 1998 and March 2013.
- Pooled odds ratios (OR) with 95% confidence intervals (CI) were calculated using fixed and random-effects models.
- The association was evaluated across dominant, recessive, additive, and codominant genetic models.
Main Results:
- The meta-analysis included 10 studies with 1529 asthma cases and 2399 controls.
- A significant association was found between CC10 +38A/G polymorphism and elevated asthma risk in the dominant model (OR = 1.62; 95% CI, 1.23-2.12; P = 0.0005).
- Subgroup analyses revealed significant associations in Asian and Caucasian populations, with other genetic models also supporting this link.
Conclusions:
- The CC10 +38A/G polymorphism is suggested to confer an increased risk of asthma.
- This genetic variant represents a potential factor in asthma susceptibility across different ethnic groups.
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