[Analysis of the Gene Mutation Type and Frequency of Thalassemia Patients in Jingzhou Area].

Q4 Medicine
Shun Liu, Cheng-Bin Li
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引用次数: 0

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 β thalassemia gene mutations.

Results: Among the 721 patients with suspected thalassemia, 228 cases were positive for α or β thalassemia gene, with a total positive rate of 31.62%, including 87 cases of α-thalassemia, accounting for 38.16%, and 140 cases of β-thalassemia, accounting for 61.40%. There was 1 case of α β 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 β-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 β-thalassemia were detected; 1 case of αβ 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 β-thalassemia, and α β complex thalassemia is relatively rare, which can provide a reference for the formulation of prevention and treatment measures for thalassemia in Jingzhou area.

[荆州地区地中海贫血患者基因突变类型及频率分析]。
目的:分析荆州地区地中海贫血患者的基因突变类型和频率:分析荆州地区地中海贫血患者的基因突变类型及频率:选取2019年6月至2022年6月在荆州市中心医院就诊的疑似地中海贫血患者共721人为研究对象。其中男性204例,女性517例。采用PCR反向点杂交法分析23种常见α或β地中海贫血基因突变的类型和频率:在721例疑似地中海贫血患者中,α或β地中海贫血基因阳性228例,总阳性率为31.62%,其中α地中海贫血87例,占38.16%,β地中海贫血140例,占61.40%。αβ复合型地中海贫血 1 例,占 0.44%。共检出 4 种α-地中海贫血基因突变类型,均为缺失型,包括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%)。在 140 名β地中海贫血患者中,138 人为纯合子,IVS-II-654M(63/140,45.00%)、CD41-42M(34/140,24.29%)、CD17M(18/140,12.86%)和 CD27-28M (10/140,7.14%)的基因型占 89.29%(125/140),发现2例双杂合子(2/140,1.43%),未发现同型β地中海贫血;发现1例基因型为-α3.7/IVS-II-654M的αβ复合型地中海贫血。不同类型地中海贫血的发病率具有统计学意义(χ2=194.250,P<0.001)。男女疑似患者的地中海贫血基因阳性率无明显差异(χ2=0.199,P=0.655):荆州地区α地中海贫血基因突变以αα/--SEA为主,β地中海贫血中以IVS-II-654M突变多见,αβ复合型地中海贫血相对少见,可为荆州地区地中海贫血防治措施的制定提供参考。
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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
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7331
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