The impact and clinical implication of variants in the start codon of HBA gene on the phenotype of thalassemia.
10.3760/cma.j.cn511374-20240829-00461
- Author:
Bairu LAI
1
;
Yiyuan GE
;
Xiaomin MA
;
Guangkuan ZENG
;
Xiaohua YU
;
Jianlian LIANG
;
Yanbin CAO
;
Liye YANG
Author Information
1. Precision Medical Lab Center, People's Hospital of Yangjiang, Yangjiang, Guangdong 529500, China. yangleeyee@sina.com.
- Publication Type:Journal Article
- MeSH:
Humans;
Phenotype;
Codon, Initiator/genetics*;
Female;
Male;
Retrospective Studies;
alpha-Globins/genetics*;
alpha-Thalassemia/genetics*;
Hemoglobin A/genetics*;
Adult;
Mutation
- From:
Chinese Journal of Medical Genetics
2025;42(1):51-55
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the correlation between variants in the start codon of the α-globin gene and phenotypes of thalassemia, so as to provide a basis for the diagnosis and prevention of α-thalassemia.
METHODS:A retrospective study was conducted on 7 patients diagnosed by Yangjiang People's Hospital and Guangzhou Hybribio Co. Ltd., from June 2019 to October 2022. Routine blood tests and hemoglobin electrophoresis were carried out. Potential variants were identified through polymerase chain reaction (PCR) combined with Reverse dot blotting (RDB), Gap-PCR, and Sanger sequencing. This study has been approved by the Medical Ethics Committee of People's Hospital of Yangjiang (Ethics No: 20240001).
RESULTS:For the 7 patients, results of blood routine test of one case was unknown, and that of another was normal. The remaining 5 cases had presented with microcytic hypochromic anemia. The results of hemoglobin electrophoresis showed that one case had normal Hb A and slightly lower Hb A2, whilst another had significantly decreased Hb A and Hb A2, in addition with the appearance of a Hb H band. The content of Hb Bart's in four neonates was ≥ 0.4%. The remaining one case had no result. Genetic testing has identified 4 rare start codon mutations, namely HBA2: c.2delT, HBA2: c.1A>G, HBA2: c.1A>T, and HBA1: c.2T>C. Among these, Patient 1 had harbored compound heterozygous variants of HBA2: c.427T>C (Hb CS) and HBA2: c.2delT. Patient 4 had harbored compound heterozygous variants of HBA2: c.1A>G and Southeast Asian type deletion.
CONCLUSION:Heterozygotes with HBA start codon variants usually present as silent or mild thalassemia, and the symptoms of anemia may deteriorate when combined with other α-thalassemia variant. The HBA2: c.1A>T start codon variant was unreported previously in China. The detection of start codon variants has helped to clarify the causes of anemia, genetic counseling, and guidance for reproduction.
