The Genotypes and Clinical Characteristics of Thalassemia on Children in Wuhan Region.
10.19746/j.cnki.issn.1009-2137.2021.06.031
- Author:
Yan YANG
1
;
Ying-Hong LU
1
;
Yang ZHANG
2
;
A-Lan ZHAO
1
;
Xiao-Yun ZHAN
1
;
Bei WU
1
;
Pei TAN
1
;
Li-Jun WAN
1
;
Juan HUANG
3
Author Information
1. Department of Pediatric Hematology, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430070, Hubei Province, China.
2. Department of General Surgery, Central Theater General Hospital, Wuhan 430070, Hubei Province, China.
3. Department of Pediatric Hematology, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430070, Hubei Province, China,E-mail: jane_huang2006@hotmail.com.
- Publication Type:Journal Article
- MeSH:
Child;
Child, Preschool;
Genetic Testing;
Genotype;
Humans;
Infant;
Infant, Newborn;
Retrospective Studies;
alpha-Thalassemia/genetics*;
beta-Thalassemia/genetics*
- From:
Journal of Experimental Hematology
2021;29(6):1875-1880
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the genotypes and clinical characteristics of thalassemia on children in Wuhan region.
METHODS:A total of 159 patients diagnosed as thalassemia in Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology from December 2017 to December 2019. The patients were retrospectively analyzed for their types of mutations, detection rates and clinical characteristics.
RESULTS:Among the 422 samples, 159 samples were finally diagnosed as thalassemia through genetic testing, the total detection rate was 37.68%. The detection rate of α, β and αβ-thalassemia was 17.30%, 20.14% and 0.24% respectively. Among α-thalassemia, αα/-SEA was the most common one, with a composition ratio of 68.49%(50/73), followed by αα/-α3.7 (19.18%), αα/-α4.2 (6.85%) and αα/ QS (1.37%). 9 types of β-thalassemia gene mutations were detected, and the most common three mutations were IVSII-654(C→T), with a composition ratio of 40.00%, CD41-42(-TTCT) (20.00%) and CD17(A→T)(16.47%). Two novel mutations of β-thalassemia, HBB: c.92-2A＞T and HBB:c.-23A＞G were detected. Among all the positive patients, 134 (84.28%) were 0-3 years old, 19 (11.95%) were 4-6 years old, and 6 (3.77%) were 7 years of age or older. There were 147 patients with mild anemia (92.45%), 11 patients with moderate anemia (6.92%), and 1 patients with severe anemia (0.63%). The MCV of 94(59.12%) patients was lower than 65 fL, and that of 51(32.08%) patients was between 65 fL and 80 fL, while 14(8.81%) patients was higher than 80 fL. MCV in β-thalassemia group was lower than that in α-thalassemia group, and the difference showed statistically significant (P<0.05).
CONCLUSION:The genotypes of thalassemia in children in Wuhan area are diverse, and most of them are mild thalassemia, and diagnosed under 3 years old. Children with β-thalassemia have smaller red blood cell volumes than those with α-thalassemia.
