Global, regional, and national burden of glucose-6-phosphate dehydrogenase (G6PD) deficiency from 1990 to 2021: a systematic analysis of the global burden of disease study 2021.

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY
Frontiers in Genetics Pub Date : 2025-05-23 eCollection Date: 2025-01-01 DOI:10.3389/fgene.2025.1593728
Zhengyu Yu, Qiang Xiong, Zhongwang Wang, Linfeng Li, Ting Niu
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Abstract

Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency remains a significant global health burden, particularly in malaria-endemic regions. Despite advances in diagnostic capabilities and treatment strategies, the prevalence and associated disability burden continue to evolve. This study provides a comprehensive assessment of the global, regional, and national burden of G6PD deficiency from 1990 to 2021, using the Global Burden of Disease (GBD) 2021 database.

Methods: Data were retrieved from GBD 2021, covering 204 countries and territories. Prevalence, incidence, and years lived with disability (YLDs) were analyzed. Age-standardized rates (ASRs) and estimated annual percentage change (EAPC) were computed to assess trends over time. The relationship between socio-demographic index (SDI) and G6PD burden was examined using Spearman correlation analysis.

Results: In 2021, global prevalence reached 443,326,869 cases, an 80.17% increase from 1990. The highest burden was observed in South Asia, accounting for 138,159,940 cases. The largest percentage increase in prevalence was in Andean Latin America (+291.96%). G6PD deficiency burden was negatively correlated with SDI, but high SDI regions exhibited higher prevalence than expected. Age- and sex-specific analysis revealed a higher burden in males, particularly in childhood and older age groups.

Conclusion: This study underscores the growing burden of G6PD deficiency, with substantial regional disparities. The findings emphasize the need for improved screening programs, policy interventions, and resource allocation in low- and middle-income countries (LMICs). Continued surveillance is essential to mitigate the long-term health consequences of this disorder.

1990年至2021年全球、地区和国家葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症负担:2021年全球疾病负担研究的系统分析
背景:葡萄糖-6-磷酸脱氢酶(G6PD)缺乏仍然是一个重大的全球健康负担,特别是在疟疾流行地区。尽管在诊断能力和治疗策略方面取得了进展,但患病率和相关的残疾负担继续发展。本研究利用全球疾病负担(GBD) 2021数据库,对1990年至2021年G6PD缺乏症的全球、地区和国家负担进行了全面评估。方法:数据从gbd2021检索,涵盖204个国家和地区。分析患病率、发病率和残疾生活年数(YLDs)。计算年龄标准化率(ASRs)和估计年百分比变化(EAPC)以评估随时间的趋势。采用Spearman相关分析检验社会人口统计指数(SDI)与G6PD负担的关系。结果:2021年全球患病率为443,326,869例,较1990年增长80.17%。在南亚观察到的负担最高,占138 1599 940例。流行率增幅最大的是安第斯拉丁美洲(+291.96%)。G6PD缺乏负担与SDI呈负相关,但SDI高地区的患病率高于预期。年龄和性别分析显示,男性负担较高,特别是在儿童和老年群体中。结论:本研究强调了G6PD缺乏症的负担日益加重,且存在显著的地区差异。研究结果强调,低收入和中等收入国家(LMICs)需要改进筛查项目、政策干预和资源分配。持续监测对于减轻这种疾病的长期健康后果至关重要。
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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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