Volume 54, Issue 12 pp. 3908-3917
Research Article

Association of a transmembrane polymorphism of Fcγ receptor IIb (FCGR2B) with systemic lupus erythematosus in Taiwanese patients

Ji-Yih Chen

Corresponding Author

Ji-Yih Chen

Chang Gung Memorial Hospital, Taiwan, Republic of China

Ji-Yih Chen, Division of Allergy, Immunology and Rheumatology, Department of Medicine, Chang Gung Memorial Hospital, No. 5 Fu-Shin Street Kuei-Shan, Tao-Yuan, Taiwan, Republic of China

Jianming Wu, Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Shelby 202, 1825 University Boulevard, Birmingham, AL 35294-0006

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Chin Man Wang

Chin Man Wang

Chang Gung Memorial Hospital, Taiwan, Republic of China

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Chung-Chun Ma

Chung-Chun Ma

Chang Gung Memorial Hospital, Taiwan, Republic of China

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Shue-Fen Luo

Shue-Fen Luo

Chang Gung Memorial Hospital, Taiwan, Republic of China

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Jeffrey C. Edberg

Jeffrey C. Edberg

University of Alabama at Birmingham

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Robert P. Kimberly

Robert P. Kimberly

University of Alabama at Birmingham

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Jianming Wu

Corresponding Author

Jianming Wu

University of Alabama at Birmingham

Ji-Yih Chen, Division of Allergy, Immunology and Rheumatology, Department of Medicine, Chang Gung Memorial Hospital, No. 5 Fu-Shin Street Kuei-Shan, Tao-Yuan, Taiwan, Republic of China

Jianming Wu, Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Shelby 202, 1825 University Boulevard, Birmingham, AL 35294-0006

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First published: 28 November 2006
Citations: 62

Abstract

Objective

To investigate the possible association of the Fcγ receptor IIb (FcγRIIb) Ile/Thr187 transmembrane domain polymorphism, which significantly affects receptor signaling, with susceptibility to systemic lupus erythematosus (SLE) in Taiwanese patients.

Methods

We used matrix-assisted laser desorption ionization−time-of-flight mass spectrometry to genotype 351 Taiwanese SLE patients and 372 age- and sex-matched healthy individuals from the same geographic area. Allele frequencies and genotype distributions were compared between the patients and controls, both as an aggregate and as stratified by sex, autoantibody profile, and clinical parameters. A combined analysis was conducted to assess the FCGR2B Thr187 allele as a common risk factor in different ethnic populations.

Results

The minor Thr187 allele was significantly associated with SLE in Taiwanese subjects (P = 0.017, odds ratio [OR] 1.989 [95% confidence interval (95% CI) 1.119–3.553]). Interestingly, male SLE patients showed enrichment of the Thr/Thr187 genotype (24%; 7 of 29) as compared with female SLE patients (10%; 32 of 322) (P = 0.043, OR 2.884 [95% CI 1.028–7.839]). Additionally, SLE patients with Thr/Thr187 and Ile/Thr187 genotypes were more likely to have pleural effusions (P = 0.038, OR 1.874 [95% CI 1.033–3.411]) and anti-SSA/Ro antibody production (P = 0.046, OR 2.221 [95% CI 1.013–4.897]). Combined analysis of 4 groups of Asian patients strongly supported the association of the FCGR2B Thr187 allele with the lupus phenotype (P = 0.000159).

Conclusion

The FcγRIIb transmembrane polymorphism is a strong disease susceptibility candidate in epistasis with other genetic effects in Taiwanese and other Asian populations. It may also play a more prominent role in male patients with SLE.

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