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Graves病白细胞减少与CTLA-4基因多态性的相关性
引用本文:杜亦陶,张勤,李梅,张鹏,邱明才.Graves病白细胞减少与CTLA-4基因多态性的相关性[J].天津医药,2005,33(10):624-626.
作者姓名:杜亦陶  张勤  李梅  张鹏  邱明才
作者单位:1. 100021,中国医学科学院附属肿瘤医院综合科
2. 300052,天津医科大学总医院内分泌科
基金项目:2002年天津市教委课题(项目编号:020201)
摘    要:目的:探讨天津地区汉族人Graves病(GD)合并白细胞减少,与细胞毒性T淋巴细胞相关抗原-H4(CTLA-4)基因外显子1第49位点A/G和启动子-318位点C/T二态性的相关性。方法:运用PCR—RFLP技术分析40例GD白细胞减少患者、56例GD白细胞正常患者及60例正常人CTLA-4基因、外显子1第49位点和启动子-318位点基因型.计算并比较各组基因型和等位基因频率。结果:GD组第1外显子第49位点基因型GG和等位基因G的频率明显高于正常对照组,3组人群的CTLA-4基因启动子-318位点的基因型与等位基因的分布差别无统计学意义。GD白细胞减少组与GD白细胞正常组之间基因型、等位基因的分布差别无统计学意义。结论:CTLA-4基因外显子1G49可能是天津地区汉族人Graves病的易感基因,而其与启动子-318位点可能不是天津地区汉族人GD合并白细胞减少的易感基因。

关 键 词:格雷夫斯病  白细胞减少  多态现象(遗传学)  基因频率  Graves病(GD)  CTLA-4基因  基因多态性  细胞毒性T淋巴细胞相关抗原  等位基因频率  基因外显子1
收稿时间:07 22 2004 12:00AM
修稿时间:2004-07-222005-05-08

Study on the Relativity of Leukopenia and Cytotoxic T Lymphocyte Associated Antigen-4 Gene Polymorphism in Graves' Disease
Du Yitao,Zhang Qin,Li Mei,Zhang Peng,Qiu Mingcai.Study on the Relativity of Leukopenia and Cytotoxic T Lymphocyte Associated Antigen-4 Gene Polymorphism in Graves'''' Disease[J].Tianjin Medical Journal,2005,33(10):624-626.
Authors:Du Yitao  Zhang Qin  Li Mei  Zhang Peng  Qiu Mingcai
Institution:Department of Endocrinology, General Hospital of Tianjin Medical University, Tianjin 300052, China
Abstract:Objective: To study the relativity of Graves'disease leukopenia and the A/G dimorphism at position 49 of exon 1 and C/T dimorphism at position 318 of promoter in cytotoxic T lymphocyte associated antigen-4 (CTLA-4) gene in Han nationality of Tianjin. Methods: The position 49 of exon 1 and position 318 of promoter gene types of CTLA-4 gene in 40 leukopenia GD patients, 56 normal leukocyte GD patients and 60 controls were analyzed by PCR-RFLP method. The gene types and allele frequencies were calculated and compared among the three groups. Results: The gene frequencies at position 49 of exon 1 GG and allele G in GD patients were significantly higher than those of the controls. There were no significant differences of the allele frequencies at position-318 of promoter in CTLA-4 gene among the three groups. There was no significant difference of gene type and allele frequency between leukopenia GD patients and normal leukocyte. Conclusion: Exon 1G49 of CTLA-4 may be the susceptible gene of GD and promoter 318 of CTLA-4 might not be the susceptible gene of leukopenia GD in Han nationality of Tianjin.
Keywords:Graves' disease leukopenia polymorphism(genetics) gene frequency
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