Interferon-induced transmembrane protein-3 genetic variant rs12252-C is associated with severe influenza in Chinese individuals.
case_control · Level III
Where this comes from
- Record sourced from PubMed, PMID 23361009.
- Also identified by DOI 10.1038/ncomms2433 and PMC identifier 3562464.
- Licence recorded as CC BY-NC-SA.
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Abstract
The SNP rs12252-C allele alters the function of interferon-induced transmembrane protein-3 increasing the disease severity of influenza virus infection in Caucasians, but the allele is rare. However, rs12252-C is much more common in Han Chinese. Here we report that the CC genotype is found in 69% of Chinese patients with severe pandemic influenza A H1N1/09 virus infection compared with 25% in those with mild infection. Specifically, the CC genotype was estimated to confer a sixfold greater risk for severe infection than the CT and TT genotypes. More importantly, because the risk genotype occurs with such a high frequency, its effect translates to a large population-attributable risk of 54.3% for severe infection in the Chinese population studied compared with 5.4% in Northern Europeans. Interferon-induced transmembrane protein-3 genetic variants could, therefore, have a strong effect of the epidemiology of influenza in China and in people of Chinese descent.
Medical subject headings
- Asian People
- Genetic Predisposition to Disease
- Influenza, Human
- Membrane Proteins
- Polymorphism, Single Nucleotide
- RNA-Binding Proteins