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用于准确诊断葡萄糖-6-磷酸脱氢酶缺乏症的综合表型和基因型方法:对泰国药物安全性的影响

Integrated Phenotypic and Genotypic Approaches for Accurate Diagnosis of G6PD Deficiency: Implications for Drug Safety in Thailand.

作者信息

Pengsuk Natnicha, Chamchoy Kamonwan, Duangdee Chatnapa, Satayarak Jantawan, Saralamba Naowarat, Nguitragool Wang, Boonyuen Usa

机构信息

Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

Princess Srisavangavadhana Faculty of Medicine, Chulabhorn Royal Academy, Bangkok, Thailand.

出版信息

Pharmacol Res Perspect. 2025 Jun;13(3):e70117. doi: 10.1002/prp2.70117.

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) deficiency holds critical health concerns, particularly due to its association with drug-induced hemolysis triggered by medications such as antimalarials. This condition poses significant risks in malaria-endemic regions where the prevalence and genetic diversity of G6PD deficiency further complicate management. Providing accurate and reliable G6PD status is vital to ensuring safe treatment, reducing complications, and improving healthcare outcomes in these populations. This study evaluated the integration of phenotypic and genotypic diagnostic methods for identifying G6PD deficiency in 2953 participants in Thailand. Using the water-soluble tetrazolium salts enzymatic assay and multiplex high-resolution melting analysis, the study revealed an overall prevalence of 3.93%, with 7.19% in males and 1.83% in females. A total of 38 distinct G6PD genotypes were identified, and zygosity was determined, highlighting significant genetic diversity, including previously unreported mutations as identified by sequencing. Hemizygous males, homozygous females, and approximately 50% of heterozygous females with missense mutations exhibited deficient or intermediate phenotypes. However, 40% of females carrying G6PD missense mutations showed a normal phenotype in quantitative phenotypic testing. The findings highlight the need for accurate G6PD diagnosis to improve drug safety and efficacy, particularly for vulnerable individuals such as heterozygous females, who are at risk of hemolysis. The cost-effective, high-throughput methods demonstrated here are suitable for large-scale screening, making them especially valuable in resource-limited settings. To maximize their impact, integrating both phenotypic and genotypic approaches into national healthcare policies and malaria programs is essential. By ensuring equitable access to reliable G6PD testing, these findings support malaria elimination efforts and address broader healthcare challenges, ultimately reducing preventable morbidity and mortality associated with G6PD deficiency.

摘要

葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症存在严重的健康问题,尤其是因为它与抗疟药等药物引发的药物性溶血有关。在疟疾流行地区,这种情况带来了重大风险,G6PD缺乏症的患病率和基因多样性使管理工作更加复杂。提供准确可靠的G6PD状态对于确保这些人群的安全治疗、减少并发症以及改善医疗结果至关重要。本研究评估了表型和基因型诊断方法在泰国2953名参与者中识别G6PD缺乏症的整合情况。通过水溶性四氮唑盐酶法和多重高分辨率熔解分析,该研究显示总体患病率为3.93%,男性为7.19%,女性为1.83%。共鉴定出38种不同的G6PD基因型,并确定了纯合性,突出了显著的基因多样性,包括测序鉴定出的以前未报告的突变。半合子男性、纯合子女性以及约50%携带错义突变的杂合子女性表现出缺乏或中间表型。然而,40%携带G6PD错义突变的女性在定量表型检测中表现出正常表型。这些发现凸显了准确诊断G6PD以提高药物安全性和疗效的必要性,特别是对于杂合子女性等易受影响的个体,她们有溶血风险。此处展示的具有成本效益的高通量方法适用于大规模筛查,使其在资源有限的环境中尤其有价值。为了最大化其影响,将表型和基因型方法整合到国家医疗政策和疟疾项目中至关重要。通过确保公平获得可靠的G6PD检测,这些发现支持疟疾消除工作并应对更广泛的医疗挑战,最终减少与G6PD缺乏症相关的可预防发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc0a/12087303/c9442297377e/PRP2-13-e70117-g003.jpg

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