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四川成都地区人群地中海贫血患者的遗传学特征分析

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目的:分析四川成都地区人群地中海贫血患者的基因突变类型及构成特点.方法:选取2017年1月至2020年12月就诊于成都市妇女儿童中心医院的6 649例疑似地贫患者的血液样本为研究对象,其中男2 273例,女4 376例,采用Luminex液相芯片法分析α、β各型地贫基因频率及分布情况.结果:6 649例患者中,检出地中海贫血基因携带者3 787例,阳性率为56.96%,其中β地贫2 063例(31.03%),α地贫1 629例(24.50%),α β复合地贫95例(1.43%).在 2 063 例 β 地贫患者中,以 CD17/N(36.45%,752/2 063)、CD41-42/N(25.30%,522/2 063)、IVS-Ⅱ-654/N(24.72%,510/2 063)为主;单纯杂合突变2 037例,占β地贫患者的98.74%.α地贫以--SEA/αα(79.01%,1 287/1 629)、-α3.7/αα(10.62%,173/1 629)、-α3.7/--SEA(2.95%,48/1 629)、-α42/αα(2.15%,35/1 629)基因型为主.α 复合 β 地贫以-α3.7/αα;CD17/N及-α3.7/αα;IVS-Ⅱ-654/N 为主,各占 α 复合 β 地贫的 14.74%(14/95).结论:四川成都地区人群β地贫比α地贫更多见,β地贫基因突变以CD17/N为主,α地贫基因突变以--SEA/αα为主,具有区域性特点.
Analysis of Genetic Characteristics of Patients with Thalassemia in the Chengdu Region,Sichuan Province
Objective:To analyze the gene mutation types and composition characteristics of patients with thalassemia in Chengdu Region,Sichuan Province.Methods:6 649 suspected thalassemia patients with positive screening results who visited Chengdu Women's and Children's Center Hospital from January 2017 to December 2020 were selected as the study subjects.Among them,there were 2 273 males and 4 376 females.The frequency and distribution of α and β genotypes of thalassemia in this cohort was analyzed by Luminex liquid-phase microarray method.Results:Among the 6 649 samples,3 787 were genetically diagnosed as thalassemia,with a total positive rate of 56.96%;in which,2 063(31.03%)cases were β-thalassemia,1 629(24.50%)cases were α-thalassemia,and 95(1.43%)cases were α combined with β thalassemia.The types of β-thalassemia gene mutation were mainly CD17/N(36.45%,752/2 063),CD41-42/N(25.30%,522/2 063),and IVS-Ⅱ-654/N(24.72%,510/2 063);and 2 037 cases of simple heterozygous mutations were identified,accounting for 98.74%of β-thalassemia patients.The types of α-thalassemia gene mutation were mainly--SEA/α α(79.01%,1 287/1 629),-α37/α α(10.62%,173/1 629),-α37/--SEA(2.95%,48/1 629),and-α42/α α(2.15%,35/1 629).The αcombined with β thalassemia was dominated by-α 3 7/α α;CD17/N and-α3 7/α α;IVS-Ⅱ-654/N,both accounting for 14.74%(14/95)of patients with α combined with β thalassemia.Conclusion:In Chengdu region,Sichuan province,βthalassemia is more common than α thalassemia,the main type of β thalassemia mutation is CD17/N,and the main type of α thalassemia mutation is--SEA/α α,with regional characteristics.

thalassemiagene detectiongenotype

舒慧英、高钰、孔庆琳、周敏

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电子科技大学医学院附属妇女儿童医院(成都市妇女儿童中心医院)儿童血液肿瘤科,四川成都 611731

地中海贫血 基因检测 基因型

2024

中国实验血液学杂志
中国病理生理学会

中国实验血液学杂志

CSTPCD北大核心
影响因子:0.988
ISSN:1009-2137
年,卷(期):2024.32(5)