The distribution and spectrum of thalassemia variants in GUIYANG region, southern China.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2025-02-07 DOI:10.1186/s13023-025-03569-8
Xuanyin Zhao, Zhiyu You, Yunyan Deng, Yi Zhou, Dongyang Deng, Jian Quan, Fang Chen, Zhimei Yan, Ya Qi, Leilei Chen, Fang Xiang, Weixian Zheng, Ruyi Zhang
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Abstract

Thalassemia is one of southern China's most common inherited disorders. This retrospective study analyzed the results of thalassemia gene testing conducted on 20,478 individuals from January 1, 2019, to April 31, 2024 in the First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine. The cohort consisted of 19,733 females and 745 males, with 1401 individuals testing positive for thalassemia. Among the positive cases, 942 had α thalassemia, 431 had β thalassemia, and 25 had variants in both α and β thalassemia genes. Interestingly, a subgroup of individuals with thalassemia variants not previously documented in medical literature was identified. The study highlighted the prevalence of thalassemia among different ethnic groups, with individuals of Han ethnicity being the most affected. Geographical analysis revealed a concentration of cases in Guizhou Province, particularly in Guiyang city, Bijie, and Qiannan Prefecture. These findings provide valuable insights into the epidemiology of thalassemia in the region and the distribution of affected individuals.

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贵阳地区地中海贫血变异的分布和谱分析。
地中海贫血是中国南方最常见的遗传性疾病之一。本回顾性研究分析了2019年1月1日至2024年4月31日在贵州中医药大学第一附属医院进行的20478例地中海贫血基因检测结果。该队列包括19,733名女性和745名男性,其中1401人地中海贫血检测呈阳性。其中α型地中海贫血942例,β型地中海贫血431例,α型和β型地中海贫血基因同时变异25例。有趣的是,研究人员发现了一组以前医学文献中没有记载的地中海贫血变异个体。该研究强调了地中海贫血在不同种族群体中的患病率,汉族个体受影响最大。地理分析显示病例集中在贵州省,特别是贵阳市、毕节和黔南州。这些发现为了解该地区地中海贫血的流行病学和受影响个体的分布提供了宝贵的见解。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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