Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis
2007

Study on CCR5 Polymorphism in Arthritis

Sample size: 2035 publication Evidence: low

Author Information

Author(s): Lindner Ewald, Nordang Gry BN, Melum Espen, Flatø Berit, Selvaag Anne Marit, Thorsby Erik, Kvien Tore K, Førre Øystein T, Lie Benedicte A

Primary Institution: Institute of Immunology, Rikshospitalet-Radiumhospitalet Medical Center

Hypothesis

Is the CCR5Δ32 polymorphism associated with rheumatoid arthritis (RA) or juvenile idiopathic arthritis (JIA) in Norwegian cohorts?

Conclusion

The study found no association between the CCR5Δ32 allele and Norwegian RA or JIA patients.

Supporting Evidence

  • The CCR5Δ32 allele frequency was 11.5% in controls vs. 10.4% in RA patients.
  • No significant negative association was observed with the Δ32 allele in either RA or JIA.
  • A revised meta-analysis reduced the initial risk estimate for RA from OR = 0.65 to OR = 0.83.

Takeaway

The researchers looked at a gene that might affect arthritis but found that it doesn't seem to play a big role in causing the disease.

Methodology

853 RA patients, 524 JIA patients, and 658 controls were genotyped for the CCR5Δ32 polymorphism.

Potential Biases

Potential publication bias in previous studies could affect the interpretation of results.

Limitations

The study may not have had enough power to detect a small effect, and results may vary between populations.

Participant Demographics

All participants were of Norwegian origin.

Statistical Information

P-Value

0.36 for RA, 0.20 for JIA

Confidence Interval

95% CI [0.71–1.14] for RA, 95% CI [0.63–1.07] for JIA

Statistical Significance

p = 0.36 for RA, p = 0.20 for JIA

Digital Object Identifier (DOI)

10.1186/1471-2350-8-33

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