Chen Ji-Yih, Wang Chin Man, Ma Chung-Chun, Luo Shue-Fen, Edberg Jeffrey C, Kimberly Robert P, Wu Jianming
Department of Medicine, Chang Gung Memorial Hospital, Taiwan, Republic of China.
Arthritis Rheum. 2006 Dec;54(12):3908-17. doi: 10.1002/art.22220.
To investigate the possible association of the Fcgamma receptor IIb (FcgammaRIIb) Ile/Thr187 transmembrane domain polymorphism, which significantly affects receptor signaling, with susceptibility to systemic lupus erythematosus (SLE) in Taiwanese patients.
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.
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).
The FcgammaRIIb 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.
研究Fcγ受体IIb(FcγRIIb)第187位异亮氨酸/苏氨酸跨膜结构域多态性(该多态性显著影响受体信号传导)与台湾地区系统性红斑狼疮(SLE)患者易感性之间的可能关联。
我们使用基质辅助激光解吸电离飞行时间质谱对351例台湾SLE患者以及来自同一地理区域的372名年龄和性别匹配的健康个体进行基因分型。比较患者和对照组之间的等位基因频率和基因型分布,整体比较以及按性别、自身抗体谱和临床参数分层比较。进行综合分析以评估FCGR2B第187位苏氨酸等位基因作为不同种族人群共同危险因素的情况。
在台湾人群中,次要的第187位苏氨酸等位基因与SLE显著相关(P = 0.017,比值比[OR] 1.989 [95%置信区间(95%CI)1.119 - 3.553])。有趣的是,与女性SLE患者(10%;322例中的32例)相比,男性SLE患者中第187位苏氨酸/苏氨酸基因型更为富集(24%;29例中的7例)(P = 0.043,OR 2.884 [95%CI 1.028 - 7.839])。此外,具有第187位苏氨酸/苏氨酸和异亮氨酸/苏氨酸基因型的SLE患者更易出现胸腔积液(P = 0.038,OR 1.874 [95%CI 1.033 - 3.411])和产生抗SSA/Ro抗体(P = 0.046,OR 2.221 [95%CI 1.013 - 4.897])。对4组亚洲患者的综合分析有力地支持了FCGR2B第187位苏氨酸等位基因与狼疮表型的关联(P = 0.000159)。
在台湾地区及其他亚洲人群中,FcγRIIb跨膜多态性是与其他遗传效应相互作用的强有力的疾病易感性候选因素。它在男性SLE患者中可能也发挥着更突出的作用。