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[Analysis of the Gene Mutation Type and Frequency of Thalassemia Patients in Jingzhou Area].
Liu, Shun; Li, Cheng-Bin.
Affiliation
  • Liu S; Department of Laboratory Medicine, Jingzhou Central Hospital, Jingzhou 434000, Hubei Province, China.
  • Li CB; Department of Laboratory Medicine, Jingzhou Central Hospital, Jingzhou 434000, Hubei Province, China. E-mail:jzlcb002@sina.com.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 32(3): 836-840, 2024 Jun.
Article in Zh | MEDLINE | ID: mdl-38926976
ABSTRACT

OBJECTIVE:

To analyze the gene mutation types and frequence of thalassemia patients in Jingzhou area.

METHODS:

A total of 721 suspected thalassemia patients who were visited in Jingzhou Central Hospital from June 2019 to June 2022 were selected as the research objects. There were 204 males and 517 females. PCR-reverse dot hybridization method was used to analyze the types and frequencies of 23 common α or ß thalassemia gene mutations.

RESULTS:

Among the 721 patients with suspected thalassemia, 228 cases were positive for α or ß thalassemia gene, with a total positive rate of 31.62%, including 87 cases of α-thalassemia, accounting for 38.16%, and 140 cases of ß-thalassemia, accounting for 61.40%. There was 1 case of α ß complex thalassemia, accounting for 0.44%. A total of 4 types of α-thalassemia gene mutations were detected, all of which were deletion types, including αα/--SEA (64/87, 73.56%), αα/-α3.7 (14/87, 16.09%), --SEA /-α3.7 (7/87, 8.05%), αα/-α4.2 (2/87, 2.30%). Among 140 patients with ß-thalassemia, 138 were pure heterozygotes, and the genotypes of IVS-II-654M (63/140, 45.00%), CD41-42M (34/140, 24.29%), CD17M (18/140, 12.86%) and CD27-28M (10/140, 7.14%) accounted for 89.29% of all mutations (125/140), 2 cases of double heterozygosity (2/140, 1.43%) were found, no homozygous ß-thalassemia were detected; 1 case of αß complex thalassemia with genotype -α3.7/IVS-II-654M was found. The incidence of difference types of thalassemia was statistically significant (χ2=194.250, P < 0.001). The percentage of positive thalassemia genes was not significantly difference between male and female suspected patients (χ2=0.199, P =0.655).

CONCLUSION:

The α-thalassemia gene mutation in Jingzhou area is dominated by αα/--SEA, and the IVS-II-654M mutation is more common in ß-thalassemia, and α ß complex thalassemia is relatively rare, which can provide a reference for the formulation of prevention and treatment measures for thalassemia in Jingzhou area.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beta-Thalassemia / Alpha-Thalassemia / Mutation Limits: Female / Humans / Male Country/Region as subject: Asia Language: Zh Journal: Zhongguo Shi Yan Xue Ye Xue Za Zhi / Zhongguo shiyan xueyexue zazhi Journal subject: HEMATOLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beta-Thalassemia / Alpha-Thalassemia / Mutation Limits: Female / Humans / Male Country/Region as subject: Asia Language: Zh Journal: Zhongguo Shi Yan Xue Ye Xue Za Zhi / Zhongguo shiyan xueyexue zazhi Journal subject: HEMATOLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: China