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G6PD Genotype and its associated enzymatic activity in a Chinese population

机译:中国人群中G6PD基因型及其相关的酶活性

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摘要

Knowledge of the G6PD genotype and its associated enzyme activity is significant for population genetics, diagnosis of disease, and management of patients. We tested 2,872 unrelated subjects from a Hakka population in China for G6PD activity by the WHO standard method and for genotype by DHPLC and DNA sequencing. Among female heterozygotes, 78.5% had relatively normal enzyme activity. The phenotype frequency of G6PD deficiency is 0.028, and the causal allele frequency is 0.060 in females. The accuracy, sensitivity, and specificity of DHPLC are more than 98% for detecting G6PD-deficient hemizygotes, heterozygotes, and homozygotes. Measuring enzyme activity alone is not sufficient for the diagnosis of heterozygotes. A combination of enzyme activity and DNA analysis should be used.
机译:G6PD基因型及其相关酶活性的知识对于人群遗传学,疾病诊断和患者管理具有重要意义。我们通过WHO标准方法测试了2872名来自中国客家人的无关受试者的G6PD活性,并通过DHPLC和DNA测序对基因型进行了测试。在女性杂合子中,有78.5%的酶活性相对正常。女性中G6PD缺乏症的表型频率为0.028,因果等位基因频率为0.060。 DHPLC的准确性,灵敏度和特异性都超过98%,可用于检测G6PD缺陷的半合子,杂合子和纯合子。仅测量酶活性不足以诊断杂合子。应同时使用酶活性和DNA分析。

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