Peng Chun-lin, Jiang Feng, Wang Bao-tao, Yang Xiao-hui, Qi Yuan-yuan, Fu Chao-wei, Qin Wan-zhang, Xu Ai-e, Wu Zhuo-chun, Meng Wei
Department of Epidemiology, School of Public Health, Fudan University, and Department of Dermatology, the Affiliated Zhongshan Hospital, Shanghai, 200032 PR China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):417-22. doi: 10.3760/cma.j.issn.1003-9406.2010.04.013.
To investigate the relationship of gene polymorphisms of programmed cell death 1 gene (PDCD1) and ultraviolet history with systemic lupus erythematosus (SLE) among the Han population in the southern region of yangtze river in China.
With a case control design, a total of 159 SLE cases and 159 controls were enrolled in this study, and single nucleotide polymorphisms (SNPs) of the PDCD1 gene were determined by PCR-restriction fragment length polymorphism (RFLP). With the aid of the logistic regression model, the effect of gene polymorphism, environmental factor and the interaction between gene and environment were fitted under the recessive, dominant, additive and codominant mode, respectively.
Three models were screened as the optimal models under the additive mode and one model under the dominant mode, according to the lowest value of Akaike's Information Criteria (AIC). After the control of age and gender, it was found that the frequency of ultraviolet exposure was higher in cases than in controls with significant difference under all models (P<0.05). For the haplotypes composed of the alleles of PD1.2, PD1.5 and PD1.6, there was significantly higher frequency of G-T-A haplotype (0.1196 vs 0.0363) and lower frequency of A-C-A haplotype (0.4746 vs 0.5399) in cases than that in controls (P<0.05) under the additive mode, and the G-T-A haplotype was associated with an increased risk for SLE (OR=4.319), while A-C-A haplotype was shown as a protective factor for SLE (OR=0.571). Moreover, interaction between A-C-G haplotype and ultraviolet exposure, which was related to an increased risk for SLE (beta5=1.182, Z=2.2898, P<0.05, OR=3.261), was also found under this mode. Additionally, the frequency of G-C-G haplotype was higher in cases than that in controls (0.1287 vs 0.0361) under the dominant mode with statistically significant difference (P<0.05, OR=4.332).
Authors' results indicate that ultraviolet exposure, G-T-A or G-C-G haplotype and interaction between A-C-G and ultraviolet exposure may be associated with genetic susceptibility to SLE in Han population in the southern region of yangtze river in China under certain genetic modes.
探讨程序性细胞死亡1基因(PDCD1)多态性及紫外线暴露史与中国长江以南地区汉族人群系统性红斑狼疮(SLE)的关系。
采用病例对照研究设计,共纳入159例SLE患者和159例对照,通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测PDCD1基因的单核苷酸多态性(SNP)。借助逻辑回归模型,分别在隐性、显性、加性和共显性模式下拟合基因多态性、环境因素以及基因与环境之间的相互作用的效应。
根据赤池信息准则(AIC)的最低值,在加性模式下筛选出3个模型作为最优模型,在显性模式下筛选出1个模型。在控制年龄和性别后,发现病例组紫外线暴露频率高于对照组,在所有模型下差异均有统计学意义(P<0.05)。对于由PD1.2、PD1.5和PD1.6等位基因组成的单倍型,在加性模式下,病例组G-T-A单倍型频率显著高于对照组(0.1196比0.0363),A-C-A单倍型频率显著低于对照组(0.4746比0.5399)(P<0.05),且G-T-A单倍型与SLE风险增加相关(OR=4.319),而A-C-A单倍型是SLE的保护因素(OR=0.571)。此外,在该模式下还发现A-C-G单倍型与紫外线暴露之间的相互作用与SLE风险增加相关(β5=1.182,Z=2.2898,P<0.05,OR=3.261)。另外,在显性模式下,病例组G-C-G单倍型频率高于对照组(0.1287比0.0361),差异有统计学意义(P<0.05,OR=4.332)。
作者的研究结果表明,在特定遗传模式下,紫外线暴露、G-T-A或G-C-G单倍型以及A-C-G与紫外线暴露之间的相互作用可能与中国长江以南地区汉族人群SLE的遗传易感性相关。