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吴晓黎, 谢渊, 齐晓岚, 何燕, 赵艳, 吴昌学, 单可人, 任锡麟. 少数民族β-地中海贫血基因突变型分布特点[J]. 中国公共卫生, 2004, 20(8): 915-916.
引用本文: 吴晓黎, 谢渊, 齐晓岚, 何燕, 赵艳, 吴昌学, 单可人, 任锡麟. 少数民族β-地中海贫血基因突变型分布特点[J]. 中国公共卫生, 2004, 20(8): 915-916.
WU Xiao-li, XIE Yuan, QI Xiao-lan, . Genotype distribution and characteristics of beta-thalassemia of Miao, Shui and Yaonationality[J]. Chinese Journal of Public Health, 2004, 20(8): 915-916.
Citation: WU Xiao-li, XIE Yuan, QI Xiao-lan, . Genotype distribution and characteristics of beta-thalassemia of Miao, Shui and Yaonationality[J]. Chinese Journal of Public Health, 2004, 20(8): 915-916.

少数民族β-地中海贫血基因突变型分布特点

Genotype distribution and characteristics of beta-thalassemia of Miao, Shui and Yaonationality

  • 摘要:
      目的   了解β-地中海贫血在贵州省苗族、水族、瑶族中的基因突变型特点、基因型频率及分布规律。
      方法   采用"红细胞休克-管定量法"测定红细胞脆性, HbF和HbA2定量等方法对人群进行β-地中海贫血初筛, 用常规酚-氯仿抽提法提取β地中海贫血携带者DNA, 经PCR-反向点杂交法对β株蛋白进行突变基因分析。
      结果   受检2566人中, 共检出134例β-地中海贫血携带者, 总检出率为522%, 其中苗族、水族、瑶族检出率分别为472%, 606%, 445%。经β珠蛋白突变基因分析, 在这3个民族中仅检出两种中国人常见突变型CD41-42和CD17, 检出率分别为88.1%, 60.0%, 23%。
      结论   在贵州省少数民族中β-地中海贫血有很高的发病率, 基因突变类型具有显著的民族特征, 并且提示在贵州省少数民族中有可能存在未知或罕见的突变类型。

     

    Abstract:
      Objective   In order to get the information about genotypes of β-thalassemia were performed in three minorities of Guizhou province, an a large-scale screening and gene analysis of β-thalassemia in Miao, Shui and Yao people.
      Methods   Red cell shocking one tube method was used to detect the erythrocyte brittleness.The HbF and HbA2 was determined by the AM-electrophoresis to detect the heterogotes of β-thalassemia.DNA extracted from white bood cells with the rountine method, then amplified and analysed by PCR and RDB(reverse dot blot)hybridization.
      Results   Among the 2 566 samples, 134 heterozygotes were found out, the incidence of the beta-thalassemia was 5.22%, the incidences in Miao, Shui and Yao people was 4.72%, 6.06%, 4.45% respectively.By gene analysis the types of majority mutation found in this area were CD41-42(-TCTT)and CD17(A→T), the dection rate in the 3 minorities were 88.1%, 60.6%, 23%.
      Conclusion   Betathalassemia had a high incidence in the minority of Guizhou, its genotypes had a marked nationality trait, the result also clewed that there were likely to exist unknown or infrequence mutation type in Guizhou minority.

     

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