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首页> 外文期刊>Genetics and molecular biology: publication of the Sociedade Brasileira de Genetica >Molecular genotyping of G6PD mutations and Duffy blood group in Afro-descendant communities from Brazilian Amazon
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Molecular genotyping of G6PD mutations and Duffy blood group in Afro-descendant communities from Brazilian Amazon

机译:巴西亚马逊裔非洲裔社区中G6PD突变和达菲血型的分子基因分型

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摘要

Abstract Glucose-6-phosphate dehydrogenase deficiency (G6PDd) and Duffy-negative blood group are two red blood cells variants that confer protection against malaria. In this study, the distribution of the most common G6PD variants (G6PD*A-, GGPD*A and G6PD Mediterranean) and the major alleles of the Duffy blood group (FY*A, FY*B and FY*BES) were investigated in an Afro-descendant population from state of Pará, Brazilian Amazon. G6PD variants and Duffy blood group alleles were determined by TaqMan SNP genotyping assay. Overall, molecular genotyping revealed the presence of G6PD variants in 126 (24%) of the individuals studied (5% male and 19% female), and frequencies of the G6PD*A- and G6PD*A alleles were 0.061 and 0.104, respectively. Duffy blood group genotyping showed that 24.3% of people were Duffy-negative and 41.3% were heterozygous for FY*BES. The frequency of allele FY*BES was 41.0%. The results emphasize the need to monitor G6PD deficiency for the use of primaquine in the routine care of the Afro-descendant communities of the Trombetas, Erepecuru and Cumná rivers, evaluating the risks of hemolytic crisis in case of recurrence of malaria in the region. In addition, the possible greater protection against malaria conferred by these erythrocyte polymorphisms deserves to be better investigated and explored among these Afro-descendants.
机译:摘要6-磷酸葡萄糖脱氢酶缺乏症(G6PDd)和达菲阴性血型是赋予抗疟疾保护作用的两种红细胞变异。在这项研究中,调查了最常见的G6PD变体(G6PD * A-,GGPD * A和G6PD地中海)和达菲血型的主要等位基因(FY * A,FY * B和FY * BES)的分布。来自巴西亚马逊州帕拉州的非洲裔。通过TaqMan SNP基因分型测定法确定G6PD变体和达菲血型等位基因。总体而言,分子基因分型显示在所研究的126位个体中(24%)(男性5%,女性19%)存在G6PD变体,G6PD * A-和G6PD * A等位基因的频率分别为0.061和0.104。 Duffy血型基因分型显示,FY * BES的人中Duffy阴性的占24.3%,杂合的占41.3%。等位基因FY * BES的发生率为41.0%。结果强调需要监测在Trombetas,Erepecuru和Cumná河的非洲后裔社区的常规护理中使用伯氨喹的G6PD缺乏症,评估该地区疟疾再次发生时发生溶血性危机的风险。此外,在这些非洲人后裔中,应该对这些红细胞多态性赋予的针对疟疾的更大的保护进行更好的研究和探索。

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