Lack of Association of Interferon Regulatory Factor 1 with Severe Malaria in Affected Child-Parental Trio Studies across Three African Populations
2009

IRF1 Locus and Severe Malaria

Sample size: 961 publication Evidence: low

Author Information

Author(s): Mangano Valentina D., Clark Taane G., Auburn Sarah, Campino Susana, Diakite Mahamadou, Fry Andrew E., Green Angela, Richardson Anna, Jallow Muminatou, Sisay-Joof Fatou, Pinder Margaret, Griffiths Michael J., Newton Charles, Peshu Norbert, Williams Thomas N., Marsh Kevin, Molyneux Malcolm E., Taylor Terrie E., Modiano David, Kwiatkowski Dominic P., Rockett Kirk A.

Primary Institution: Childhood Infection Group, The Wellcome Trust Centre for Human Genetics, Oxford, United Kingdom

Hypothesis

Does genetic variation at the IRF1 locus affect the risk of developing severe malaria?

Conclusion

The study found no significant association between IRF1 genetic variations and severe malaria in the populations tested.

Supporting Evidence

  • No significant association with severe malaria or its subphenotypes was observed for any of the SNPs tested.
  • The study included 961 trios from three different African populations.
  • IRF1 has been previously associated with the ability to control P. falciparum infection, but not with severe malaria.
  • The study used a family-based association method to avoid population stratification issues.

Takeaway

The researchers looked at genes to see if they could explain why some kids get really sick from malaria, but they didn't find any links.

Methodology

The study used a family-based test of association for 18 SNPs across the IRF1 gene in 961 trios from The Gambia, Kenya, and Malawi.

Potential Biases

Population structure may lead to false positive results.

Limitations

The study may lack power to detect small effects of IRF1 polymorphisms on severe malaria.

Participant Demographics

Participants included children with severe malaria and their parents from The Gambia, Kenya, and Malawi.

Digital Object Identifier (DOI)

10.1371/journal.pone.0004206

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