Host Genetic Risk Factors for West Nile Virus Infection and Disease Progression
2011

Genetic Risk Factors for West Nile Virus Infection and Disease Progression

Sample size: 753 publication 10 minutes Evidence: moderate

Author Information

Author(s): Bigham Abigail W., Buckingham Kati J., Husain Sofia, Emond Mary J., Bofferding Kathryn M., Gildersleeve Heidi, Rutherford Ann, Astakhova Natalia M., Perelygin Andrey A., Busch Michael P., Murray Kristy O., Sejvar James J., Green Sharone, Kriesel John, Brinton Margo A., Bamshad Michael

Primary Institution: University of Washington

Hypothesis

Identifying genetic factors that influence the development of West Nile virus disease could help elucidate pathways important for increased pathogenicity.

Conclusion

The study found that genetic variations in the interferon response pathway are associated with both the risk of symptomatic West Nile virus infection and disease progression.

Supporting Evidence

  • SNPs in IRF3 and MX1 were associated with symptomatic West Nile virus infection.
  • A single SNP in OAS1 was associated with increased risk for West Nile encephalitis and paralysis.
  • Genetic variation in the interferon response pathway is linked to disease progression.

Takeaway

Some people get really sick from West Nile virus while others don't, and this study found that our genes might help explain why.

Methodology

The study involved a case-control association analysis of SNPs in 86 genes among 753 individuals infected with West Nile virus.

Potential Biases

Potential biases may arise from the selection of control groups and the classification of disease phenotypes.

Limitations

The study's findings may not be generalizable due to the specific population studied and the reliance on self-reported ancestry.

Participant Demographics

The study included 753 individuals, with 422 symptomatic cases and 331 asymptomatic cases, with a median age of 57 for symptomatic cases.

Statistical Information

P-Value

0.003

Confidence Interval

95% CI 3.60–26.61

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0024745

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