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Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China

Background: There are limited studies on the molecular profile of thalassemia in Hainan, the free trade island in China. Our aim was to reveal the prevalence and molecular mutation spectrum of thalassemia in different ethnic groups and regions of Hainan through a large sample study for the first tim...

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Autores principales: Wang, Min, Zhang, Xiaozhuang, Zhang, Yubin, Xiao, Meifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245582/
https://www.ncbi.nlm.nih.gov/pubmed/35783269
http://dx.doi.org/10.3389/fgene.2022.874624
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author Wang, Min
Zhang, Xiaozhuang
Zhang, Yubin
Xiao, Meifang
author_facet Wang, Min
Zhang, Xiaozhuang
Zhang, Yubin
Xiao, Meifang
author_sort Wang, Min
collection PubMed
description Background: There are limited studies on the molecular profile of thalassemia in Hainan, the free trade island in China. Our aim was to reveal the prevalence and molecular mutation spectrum of thalassemia in different ethnic groups and regions of Hainan through a large sample study for the first time. Methods: A total of 231,596 individuals from 19 cities and counties in Hainan were screened by hematological parameter analysis, and further genetic analysis was performed on individuals with MCV less than 82 fL. Results: Totally, 31,780 (13.72%) subjects were diagnosed as thalassemia carriers. The overall prevalence of α-thalassemia, β-thalassemia, and α+β-thalassemia were 11.04%, 1.48%, and 1.20%, respectively. We further analyzed the molecular profiles of thalassemia in various ethnic groups and mainly compared the difference between Han and Li. The results showed that the frequency of thalassemia in the Li population (47.03%) was much higher than that in Han (9.37%). Except for β-thalassemia (1.31% of Li vs. 1.47% of Han), the frequencies of α-thalassemia (39.59% of Li vs. 7.35% of Han) and α+β-thalassemia (6.13% of Li vs. 0.56% of Han) in the Li were obviously higher than those in Han. The high-frequent genotypes of α-thalassemia in Han were αα/--(SEA) (25.55%), -α(3.7)/αα (22.17%), -α(4.2)/αα (21.59%), α(WS)α/αα (8.93%), and -α(3.7)/-α(4.2) (4.17%) and those of Li were -α(4.2)/αα (17.24%), -α(3.7)/αα (17.16%), -α(3.7)/-α(4.2) (15.09%), α(WS)α/αα (9.69%), and α(WS)α/-α(3.7) (8.06%), respectively. The αα/--(SEA) was the highest genotype of α-thalassemia in Han but only accounted for 1.87% in Li. For β-thalassemia, the top three high-frequent genotypes in both Han and Li were β(CD41/42(-TTCT))/β(N), β(-28(A>G))/β(N), and β(IVS-Ⅱ-654(C>T))/β(N), but the frequency of β(CD41/42(-TTCT))/β(N) in Li (90.96%) was much higher than that in Han (56.32%) and the data reported in other provinces of China. Additionally, the prevalence of thalassemia ranged from 8.16% to 34.35% in Hainan, Wuzhishan, Baoting, Qiongzhong, and Baisha have a higher prevalence than other areas. Conclusion: Our study revealed the characteristics of ethnic and regional differences in the prevalence of thalassemia in the childbearing age population of Hainan for the first time, indicating that the prevalence of thalassemia among Li nationality is the highest in China. Those findings will be useful for genetic counseling and the prevention of thalassemia.
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spelling pubmed-92455822022-07-01 Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China Wang, Min Zhang, Xiaozhuang Zhang, Yubin Xiao, Meifang Front Genet Genetics Background: There are limited studies on the molecular profile of thalassemia in Hainan, the free trade island in China. Our aim was to reveal the prevalence and molecular mutation spectrum of thalassemia in different ethnic groups and regions of Hainan through a large sample study for the first time. Methods: A total of 231,596 individuals from 19 cities and counties in Hainan were screened by hematological parameter analysis, and further genetic analysis was performed on individuals with MCV less than 82 fL. Results: Totally, 31,780 (13.72%) subjects were diagnosed as thalassemia carriers. The overall prevalence of α-thalassemia, β-thalassemia, and α+β-thalassemia were 11.04%, 1.48%, and 1.20%, respectively. We further analyzed the molecular profiles of thalassemia in various ethnic groups and mainly compared the difference between Han and Li. The results showed that the frequency of thalassemia in the Li population (47.03%) was much higher than that in Han (9.37%). Except for β-thalassemia (1.31% of Li vs. 1.47% of Han), the frequencies of α-thalassemia (39.59% of Li vs. 7.35% of Han) and α+β-thalassemia (6.13% of Li vs. 0.56% of Han) in the Li were obviously higher than those in Han. The high-frequent genotypes of α-thalassemia in Han were αα/--(SEA) (25.55%), -α(3.7)/αα (22.17%), -α(4.2)/αα (21.59%), α(WS)α/αα (8.93%), and -α(3.7)/-α(4.2) (4.17%) and those of Li were -α(4.2)/αα (17.24%), -α(3.7)/αα (17.16%), -α(3.7)/-α(4.2) (15.09%), α(WS)α/αα (9.69%), and α(WS)α/-α(3.7) (8.06%), respectively. The αα/--(SEA) was the highest genotype of α-thalassemia in Han but only accounted for 1.87% in Li. For β-thalassemia, the top three high-frequent genotypes in both Han and Li were β(CD41/42(-TTCT))/β(N), β(-28(A>G))/β(N), and β(IVS-Ⅱ-654(C>T))/β(N), but the frequency of β(CD41/42(-TTCT))/β(N) in Li (90.96%) was much higher than that in Han (56.32%) and the data reported in other provinces of China. Additionally, the prevalence of thalassemia ranged from 8.16% to 34.35% in Hainan, Wuzhishan, Baoting, Qiongzhong, and Baisha have a higher prevalence than other areas. Conclusion: Our study revealed the characteristics of ethnic and regional differences in the prevalence of thalassemia in the childbearing age population of Hainan for the first time, indicating that the prevalence of thalassemia among Li nationality is the highest in China. Those findings will be useful for genetic counseling and the prevention of thalassemia. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9245582/ /pubmed/35783269 http://dx.doi.org/10.3389/fgene.2022.874624 Text en Copyright © 2022 Wang, Zhang, Zhang and Xiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Wang, Min
Zhang, Xiaozhuang
Zhang, Yubin
Xiao, Meifang
Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China
title Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China
title_full Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China
title_fullStr Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China
title_full_unstemmed Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China
title_short Prevalence and Genetic Analysis of Thalassemia and Hemoglobinopathy in Different Ethnic Groups and Regions in Hainan Island, Southeast China
title_sort prevalence and genetic analysis of thalassemia and hemoglobinopathy in different ethnic groups and regions in hainan island, southeast china
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245582/
https://www.ncbi.nlm.nih.gov/pubmed/35783269
http://dx.doi.org/10.3389/fgene.2022.874624
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