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Letter

ITGAV polymorphism and disease susceptibility in a Japanese rheumatoid arthritis population

Noriko Iikuni, Shu Kobayashi, Katsunori Ikari*, Taisuke Tomatsu, Masako Hara, Hisashi Yamanaka, Naoyuki Kamatani and Shigeki Momohara

Author Affiliations

Institute of Rheumatology, Tokyo Women's Medical University, 10-22 Kawada, Tokyo, 162-0054 Japan

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Arthritis Research & Therapy 2007, 9:405  doi:10.1186/ar2303


See related research by Jacq et al., http://arthritis-research.com/content/9/4/R63 and related editorial by Ahnert and Kirsten, http://arthritis-research.com/content/9/5/108

The electronic version of this article is the complete one and can be found online at: http://arthritis-research.com/content/9/5/405


Published:31 October 2007

© 2007 BioMed Central Ltd

Letter

A research article by Jacq and colleagues [1], recently published in this journal, reported an association between rheumatoid arthritis (RA) and the rs3738919-C allele in the ITGV gene, which encodes the αv subunit of the integrin αvβ3, in a European Caucasian population.

One feature of the pathophysiology of RA is the hyper-angiogenesis observed in the synovial tissue and, along with excess macrophages and T lymphocytes, αvβ3 ligands are also abundant in synovial fluid [2]. As a key player in angiogenesis [3], it has been suggested that ITGAV may be a RA susceptibility gene. The linkage study also supports this view because the 2q31 region containing ITGAV exhibited linkage in a dense genome scan [4].

Although the European association study by Jacq and colleagues [1] indicated ITGAV to be a new minor RA susceptibility gene, a replication study conducted in a population of different ethnicity is helpful in exploring whether the association is caused by a common variance through various ethnic groups. We therefore undertook a large population-based study to investigate the association between ITGAV and RA in a Japanese population.

DNA samples were obtained from 1,504 Japanese RA patients and 449 population control individuals [5]. Genotypes were determined using the TaqMan method, in accordance with the manufacturer's instructions (Applied Biosystems, Tokyo, Japan). Table 1 shows the genotype distributions and allelic frequencies of patients and control individuals. Unlike the European population, the rs3738919-C allele was more frequent in control individuals in our Japanese population, and no significant differences were observed in allele frequencies for Japanese RA patients and control individuals (0.908 and 0.922, respectively).

Table 1. Distribution of ITGAV rs3738919 genotypes in Japanese rheumatoid arthritis patients and control individuals

There are several factors that must be accounted for when a study fails to corroborate a previously identified association. One of these is an ethnicity-specific effect. Ethnic differences can result in differences in allele frequencies, and the genetic background of the disease itself may vary between ethnic groups. Another issue that must be considered is that, usually, negative association studies of a target gene outside the HLA region lack sufficient power to detect the genetic effect because the disease-associated genes outside the region may be associated with limited relative risk for disease susceptibility. While considering the odds ratio of Jacq et al.'s study [1], our study was designed to have sufficient power to detect the effect of the ITGAV gene (> 0.96; number of cases = 1504, number of controls = 449, OR in the original French study [1] = 1.94, frequency of rs3738919-A allele in the controls = 0.078, significance level = 0.05). However, when the odds ratio is under 1.67, the power is limited to below 0.8, and this may represent a study limitation.

Despite its association with RA in Caucasian populations, an association of the ITGAV gene with RA patients in the Japanese was not observed. Further studies in other ethnic groups are necessary to draw definite conclusions.

Competing interests

The authors declare that they have no competing interests.

References

  1. Jacq L, Garnier S, Dieude P, Michou L, Pierlot C, Migliorini P, Balsa A, Westhovens R, Barrera P, Alves H, et al.: The ITGAV rs3738919-C allele is associated with rheumatoid arthritis in the European Caucasian population: a family-based study.

    Arthritis Res Ther 2007, 9:R63. PubMed Abstract | BioMed Central Full Text OpenURL

  2. Friedlander M, Brooks PC, Shaffer RW, Kincaid CM, Varner JA, Cheresh DA: Definition of two angiogenic pathways by distinct alpha v integrins.

    Science 1995, 270:1500-1502. PubMed Abstract | Publisher Full Text OpenURL

  3. Eliceiri BP, Cheresh DA: The role of alphav integrins during angiogenesis: insights into potential mechanisms of action and clinical development.

    J Clin Invest 1999, 103:1227-1230. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  4. Osorio YFJ, Bukulmez H, Petit-Teixeira E, Michou L, Pierlot C, Cailleau-Moindrault S, Lemaire I, Lasbleiz S, Alibert O, Quillet P, et al.: Dense genome-wide linkage analysis of rheumatoid arthritis, including covariates.

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  5. Iwamoto T, Ikari K, Inoue E, Toyama Y, Hara M, Yamanaka H, Tomatsu T, Momohara S, Kamatani N: Failure to confirm association between PDCD1 polymorphisms and rheumatoid arthritis in a Japanese population.

    J Hum Genet 2007, 52:557-560. PubMed Abstract | Publisher Full Text OpenURL