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首页> 外文期刊>Malaria Journal >Genotypic and phenotypic characterization of G6PD deficiency in Bengali adults with severe and uncomplicated malaria
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Genotypic and phenotypic characterization of G6PD deficiency in Bengali adults with severe and uncomplicated malaria

机译:孟加拉人患有严重和不复杂疟疾的成年人中G6PD缺乏症的基因型和表型特征

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BackgroundControl of malaria increasingly involves administration of 8-aminoquinolines, with accompanying risk of haemolysis in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency. Few data on the prevalence and genotypic basis of G6PD deficiency are available from Bangladesh, where malaria remains a major problem in the South (Chittagong Division). The aim of this study was to determine the prevalence of G6PD deficiency, and associated G6PD genotypes, in adults with falciparum malaria in southern Bangladesh. MethodsG6PD status was assessed via a combination of fluorescent spot testing (FST) and genotyping in 141 Bengali patients admitted with falciparum malaria to two centres in Chittagong Division from 2012 to 2014. In addition, an analysis of genomic data from 1000 Genomes Project was carried out among five healthy Indian subcontinent populations. ResultsOne male patient with uncomplicated malaria was found to have G6PD deficiency on FST and a genotype associated with deficiency (hemizygous Orissa variant). In addition, there were two female patients heterozygous for deficiency variants (Orissa and Kerala-Kalyan). These three patients had a relatively long duration of symptoms prior to admission compared to G6PD normal cases, possibly suggesting an interaction with parasite multiplication rate. In addition, one of 27 healthy local controls was deficient on FST and hemizygous for the Mahidol variant of G6PD deficiency. Examination of 1000 Genomes Project sequencing data across the Indian subcontinent showed that 19/723 chromosomes (2.63%) carried a variant associated with deficiency. In the Bengali from Bangladesh 1000 Genomes population, three of 130 chromosomes (2.31%) carried deficient alleles; this included single chromosomes carrying the Kerala-Kalyan and Orissa variants. ConclusionsIn line with other recent work, G6PD deficiency is uncommon in Bengalis in Bangladesh. Further studies of particular ethnic groups are needed to evaluate the potential risk of wide deployment of primaquine in malaria control efforts in Bangladesh.
机译:背景疟疾控制越来越多地涉及使用8-氨基喹啉,同时伴有葡萄糖-6-磷酸脱氢酶(G6PD)缺乏者的溶血风险。孟加拉国缺乏关于G6PD缺乏症患病率和基因型基础的数据,孟加拉国南部仍然是疟疾的主要问题(吉大港分部)。这项研究的目的是确定孟加拉国南部患有恶性疟疾的成年人中G6PD缺乏症的患病率以及相关的G6PD基因型。方法通过荧光斑点试验(FST)和基因分型相结合的方法,对2012年至2014年在吉大港市两个中心的141名孟加拉恶性疟患者进行基因分型,以评估其G6PD的状态。此外,还对1000个基因组计划的基因组数据进行了分析。五个健康的印度次大陆人口中。结果发现一名患有单纯性疟疾的男性患者在FST上存在G6PD缺乏症,并伴有与缺乏症相关的基因型(半合Orissa变异)。此外,有两名女性患者因缺乏症而杂合(Orissa和Kerala-Kalyan)。与G6PD正常病例相比,这三名患者入院前的症状持续时间相对较长,可能表明与寄生虫繁殖率存在相互作用。另外,27个健康的本地对照中的一个在FST和半合子方面缺乏G6PD的Mahidol变体。检验印度次大陆的1000个基因组计划测序数据表明,19/723染色体(2.63%)带有与缺陷相关的变异。在孟加拉国来自孟加拉国1000个基因组的人口中,130条染色体中的3条(2.31%)携带有缺陷等位基因;其中包括携带Kerala-Kalyan和Orissa变体的单条染色体。结论与最近的其他工作一样,孟加拉国孟加拉国很少发生G6PD缺乏症。需要对特定族裔进行进一步研究,以评估在孟加拉国控制疟疾工作中广泛使用伯氨喹的潜在风险。

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