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The gene spectrum of thalassemia in Yangjiang of western Guangdong Province.

Authors :
Liang HF
Liang WM
Xie WG
Lin F
Liu LL
Li LJ
Ge YY
Lu M
Liao YW
Zeng GK
Yao JX
Situ JW
Yang LY
Source :
Frontiers in genetics [Front Genet] 2023 Feb 13; Vol. 14, pp. 1126099. Date of Electronic Publication: 2023 Feb 13 (Print Publication: 2023).
Publication Year :
2023

Abstract

Background: Thalassemia presents a higher incidence in southern China. The objective of this study is to analyze the genotype distribution of thalassemia in Yangjiang, a western city of Guangdong Province in China. Methods: The genotypes of suspected cases with thalassemia were tested by PCR and reverse dot blot (RDB). Unidentified rare thalassemia genotypes of the samples were further ascertained by PCR and direct DNA sequencing. Results: Among 22467 suspected cases with thalassemia, 7658 cases were found with thalassemia genotypes using our PCR-RDB kit. Among these 7658 cases, 5313 cases were found with α-thalassemia (α-thal) alone, -- <superscript>SEA</superscript> /αα was the most common genotype, accounting for 61.75% of α-thal genotypes, and the following mutations were found: α <superscript>3.7</superscript> /αα, -α <superscript>4.2</superscript> /αα, α <superscript>CS</superscript> α/αα, α <superscript>WS</superscript> α/αα, and α <superscript>QS</superscript> α/αα. A total of 2032 cases were found with β-thalassemia (β-thal) alone. β <superscript>CD41-42</superscript> /β <superscript>N</superscript> , β <superscript>IVS-II-654</superscript> /β <superscript>N</superscript> , and β <superscript>-28</superscript> /β <superscript>N</superscript> accounted for 80.9% of all β-thal genotypes, and the following genotypes were found: β <superscript>CD17</superscript> /β <superscript>N</superscript> , β <superscript>CD71-72</superscript> /β <superscript>N</superscript> , and β <superscript>E</superscript> /β <superscript>N</superscript> . Compound heterozygotes of β-thal and β-thalassemia homozygotes were identified in 11 and five cases, respectively, in this study. α-thal combined with β-thal was identified in 313 cases, showing 57 genotype combinations of the coincidence of both Hb disorders; one extreme patient had a genotype of -- <superscript>SEA</superscript> /α <superscript>WS</superscript> α and β <superscript>CD41-42</superscript> /β <superscript>-28</superscript> . In addition, four rare α -mutations (-- <superscript>THAI</superscript> , HKαα, Hb Q-Thailand, and CD31 AGG>AAG) and six rare β-mutations (CD39 CAG>TAG, IVS-Ⅱ-2 (-T), -90(C>T), Chinese <superscript>G</superscript> γ <superscript>+</superscript> (Aγδβ)0, CD104 (-G), and CD19 A>G) were also found in this study population. Conclusion: This study provided detailed genotypes of thalassemia in Yangjiang of western Guangdong Province in China and reflected the complexity of genotypes in this high-prevalence region, and this would be valuable for diagnosis and counseling for thalassemia in this area.<br />Competing Interests: Authors L-JL, Y-YG, and ML were employed by Guangdong Hybribio Limited Corporation. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Liang, Liang, Xie, Lin, Liu, Li, Ge, Lu, Liao, Zeng, Yao, Situ and Yang.)

Details

Language :
English
ISSN :
1664-8021
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in genetics
Publication Type :
Academic Journal
Accession number :
36861132
Full Text :
https://doi.org/10.3389/fgene.2023.1126099