Analysis of genotype distribution of thalassemia and G6PD deficiency among Hakka population in Meizhou city of Guangdong Province

被引:8
作者
Wu, Heming [1 ,2 ,3 ,4 ]
Zhu, Qiuyan [1 ,2 ,3 ,4 ]
Zhong, Hua [1 ,2 ,3 ,4 ]
Yu, Zhikang [1 ,2 ,3 ,4 ]
Zhang, Qunji [1 ,2 ,3 ,4 ]
Huang, Qingyan [1 ,2 ,3 ,4 ]
机构
[1] Sun Yat Sen Univ, Meizhou Hosp, Meizhou Acad Med Sci, Meizhou Peoples Hosp,Huangtang Hosp,Ctr Precis Me, Meizhou, Peoples R China
[2] Sun Yat Sen Univ, Guangdong Prov Key Lab Precis Med & Clin Translat, Meizhou Acad Med Sci, Meizhou Peoples Hosp,Huangtang Hosp,Meizhou Hosp, Meizhou, Peoples R China
[3] Guangdong Prov Engn & Technol Res Ctr Clin Mol Di, Meizhou, Peoples R China
[4] Sun Yat Sen Univ, Meizhou Municipal Engn & Technol Res Ctr Mol Diag, Meizhou Acad Med Sci, Meizhou Peoples Hosp,Huangtang Hosp,Meizhou Hosp, Meizhou, Peoples R China
关键词
G6PD; genotype distribution; Meizhou city; southern China; thalassemia; BETA-THALASSEMIA; GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY; MOLECULAR CHARACTERIZATION; HEMOGLOBIN DISORDERS; AUTONOMOUS REGION; HIGH PREVALENCE; SOUTH CHINA; ALPHA; SPECTRUM; GUANGXI;
D O I
10.1002/jcla.23140
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective The aim of the study was to explore genotype distribution thalassemia and G6PD deficiency in Meizhou city, China. Methods A total of 16 158 individuals were involved in thalassemia genetic testing. A total of 605 subjects were screened for common Chinese G6PD mutations by gene chip analysis. Genotypes and allele frequencies were analyzed. Results A total of 5463 cases carried thalassemia mutations were identified, including 3585 cases, 1701 cases, and 177 cases with alpha-, beta-, and alpha + beta-thalassemia mutations, respectively. --(SEA) (65.12%), -alpha(3.7) (19.05%), and -alpha(4.2) (8.05%) deletion were the main mutations of alpha-thalassemia, while IVS-II-654(C -> T) (40.39%), CD41-42(-TCTT) (32.72%), -28(A -> G) (10.11%), and CD17(A -> T) (9.32%) mutations were the principal mutations of beta-thalassemia in Meizhou. There were significant differences in allele frequencies in some counties. Genetic testing for G6PD deficiency, six mutation sites, and one polymorphism were detected in our study. A total of 198 alleles with the mutation were detected among 805 alleles (24.6%). G6PD Canton (c.1376 G -> T) (45.96%), G6PD Kaiping (c.1388 G -> A) (39.39%), and G6PD Gaohe (c.95 A -> G) (9.09%) account for 94.44% mutations, followed by G6PD Chinese-5 (c.1024 C -> T) (4.04%), G6PD Viangchan (c.871G -> A) (1.01%), and G6PD Maewo (c.1360 C -> T) (0.51%). There were some differences of the distribution of G6PD mutations among eight counties in Meizhou. Conclusions The --(SEA), -alpha(3.7), and -alpha(4.2) deletion were the main mutations of alpha-thalassemia, while IVS-II-654(C -> T), CD41-42(-TCTT), -28(A -> G), and CD17(A -> T) mutations were the principal mutations of beta-thalassemia in Meizhou. G6PD c.1376 G -> T, c.1388 G -> A, and c.95 A -> G were the main mutations of G6PD deficiency. There were some differences of the distribution of thalassemia and G6PD mutations among eight counties in Meizhou.
引用
收藏
页数:9
相关论文
共 23 条
  • [21] Screening results and mutation frequency analysis of G6PD deficiency in 1,291,274 newborns in Huizhou, China: a twenty-year experience
    Zhiqiang Zhang
    Xiaoting Wang
    Jianhui Jiang
    Annals of Hematology, 2024, 103 : 29 - 36
  • [22] Screening results and mutation frequency analysis of G6PD deficiency in 1,291,274 newborns in Huizhou, China: a twenty-year experience
    Zhang, Zhiqiang
    Wang, Xiaoting
    Jiang, Jianhui
    ANNALS OF HEMATOLOGY, 2024, 103 (01) : 321 - 334
  • [23] A community based study on haemoglobinopathies and G6PD deficiency among particularly vulnerable tribal groups in hard-to-reach malaria endemic areas of Odisha, India: implications on malaria control
    Sujata Dixit
    Arundhuti Das
    Ramakanta Rana
    Hemant K. Khuntia
    Akhil B. Ota
    Sanghamitra Pati
    Madhusmita Bal
    Manoranjan Ranjit
    Malaria Journal, 21