A Large-Scale Rheumatoid Arthritis Genetic Study Identifies Association at Chromosome 9q33.2 TRAF1 Variants on Chr 9q33.2 and RA
2008

Genetic Study Identifies Risk Factors for Rheumatoid Arthritis

Sample size: 1732 publication 10 minutes Evidence: high

Author Information

Author(s): Chang Monica, Rowland Charles M., Garcia Veronica E., Schrodi Steven J., Catanese Joseph J., van der Helm-van Mil Annette H. M., Ardlie Kristin G., Amos Christopher I., Criswell Lindsey A., Kastner Daniel L., Gregersen Peter K., Kurreeman Fina A. S., Toes Rene E. M., Huizinga Tom W. J., Seldin Michael F., Begovich Ann B.

Primary Institution: Celera, Alameda, California, United States of America

Hypothesis

Can we identify additional genetic risk factors for rheumatoid arthritis beyond the known markers?

Conclusion

The study found significant associations between specific genetic variants on chromosome 9q33.2 and an increased risk of rheumatoid arthritis.

Supporting Evidence

  • Identified a SNP, rs1953126, significantly associated with RA.
  • Combined analysis across three sample sets showed strong statistical significance.
  • Variants reported generate more than a 45-fold RA-risk differential when combined with other known risk factors.

Takeaway

Researchers looked at the DNA of people with rheumatoid arthritis and found new genes that might make some people more likely to get the disease.

Methodology

The study used a multi-tiered, case-control association approach, genotyping 25,966 SNPs in multiple independent sample sets.

Potential Biases

Potential bias due to population stratification and the focus on specific ethnic groups.

Limitations

The study primarily focused on white North American and Dutch populations, which may limit the generalizability of the findings.

Participant Demographics

Participants included white North American and Dutch individuals, with a mix of rheumatoid factor-positive and negative patients.

Statistical Information

P-Value

1.45E-06

Confidence Interval

95% CI 1.16–1.40

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pgen.1000107

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