杀菌/通透性增加蛋白基因Glu216Lys多态性与中国汉族人群炎症性肠病无关  被引量:3

Glu216Lys polymorphism of bactericidal/permeability-increasing protein gene has no association with inflammatory bowel disease in Chinese Han population

在线阅读下载全文

作  者:杨庆帆[1] 陈白莉[1] 张青森[1] 何瑶[1] 陈旻湖[1] 曾志荣[1] 

机构地区:[1]中山大学附属第一医院消化内科,广东广州510080

出  处:《中国病理生理杂志》2013年第4期718-723,共6页Chinese Journal of Pathophysiology

摘  要:目的:探讨杀菌/通透性增加蛋白(BPI)基因Glu216Lys多态性与中国汉族人群炎症性肠病(IBD)发病及各种临床特征的相关性。方法:纳入286例确诊的汉族IBD患者[173例克罗恩病(CD)和113例溃疡性结肠炎(UC)]及年龄、性别匹配的332名健康人进行病例对照研究。采用引物介导的限制性分析PCR方法检测基因分型;应用单因素分析和Logistic回归模型分析该位点多态性对IBD发病及临床特征的影响。结果:CD和UC病例组与正常对照组间Glu216Lys基因型和等位基因频率差异均无统计学意义(均P>0.05);进一步分析Glu216Lys与CD和UC的临床特征关系,差异均无统计学意义(P>0.05)。结论:BPI基因Glu216Lys多态性与中国汉族人群IBD发病和临床特征无明显相关。IBD的遗传易感性具有种族差异性。AIM: To investigate the association between Glu216Lys polymorphism of bactericidal/pormeability- increasing protein (BPI) gene and inflammatory bowel disease (IBD) in Chinese Han population and to elucidate the' po- tential interactions between genotypes and clinical features. METHODS: The single nucleotide polymorphism (SNP) of Glu216Lys was genotyped in 286 IBD patients, including 173 Crohn disease (CD) and 113 ulcerative colitis (UC) cases, and 332 age- and sex-matched healthy controls by primer-introduced restriction analysis PCR (PIRA-PCR). Univariate a- nalysis and Logistic regression model were used to evaluate the influences of Glu21fLys polymorphism on IBD clinical fea- tures. RESULTS : No significant difference in the frequency of the genotypes and alleles between cases and controls ( CD group vs control group, P 〉 0.05; UC group vs control group, P 〉 0. 05) was observed. Glu216Lys polymorphism had no relationship with the clinical types of UC and CD (P 〉0. 05). CONCLUSION: The SNP of Glu216Lys in BPI is not as- sociated with IBD in Chinese Han population. The contribution of genetic determinants is significantly different among eth- nicities.

关 键 词:炎症性肠病 杀菌 通透性增加蛋白 单核苷酸多态性 中国汉族人群 

分 类 号:R392.2[医药卫生—免疫学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象