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咸宁市地中海贫血的基因突变类型及血液学特征分析

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目的 通过描述性研究全面了解咸宁市人群地中海贫血患者的检出率、基因突变类型、分布特征、性别差异以及血液学特征.方法 收集我院门诊及住院治疗中进行地中海贫血基因检测的患者共 3105 例,采集所有纳入研究样本人群的EDTA抗凝血,进行血常规检测,同时用PCR-反向点杂交法检测α和β地中海贫血基因,通过显色的方式判断样本基因型.结果 3105 例样本中经地贫基因检测确诊地中海贫血的患者 223 例,阳性检出率为7.18%.其中男32 例,女 191 例,在性别分布上无明显差异(Χ2=0.189,P=0.663).确诊患者中α-地贫基因阳性样本为占 125 例,为56.05%;β-地贫基因阳性样本占95 例,为42.60%;另外αβ-地贫基因阳性样本仅占3 例,为 1.35%.本研究共检测出 8 种α-地中海贫血基因型,主要的基因型是-α3.7/αα、--SEA/αα和-α4.2/αα,分别占45.60%、37.60%和9.60%,占所有α地中海贫血突变携带者的 92.80%;β-地中海贫血基因型共检测出 11 种,主要的基因型是 β654/βN、β41-42/βN 和 β17/βN,分别占 43.16%、28.43%和9.47%;αβ-复合型地贫共检测出 3 例,基因型分别为-α3.7/αα&β41-42βN、--SEA/αα&β41-42/βN、-α4.2/αα&βIVS-Ⅱ-654/βN.对正常组、α-地贫组、β-地贫组的相关血液学指标包括血红蛋白(Hb)、平均红细胞体积(MCV)、平均血红蛋白量(MCH)、平均血红蛋白浓度(MCHC)进行比较,差异有统计学意义(P<0.05).结论 咸宁市地贫阳性检出率及基因型与湖北省其他地区有差异,检测地贫基因,对提高咸宁区域地贫防治进而引导优生优育可提供帮助,并且血常规中红细胞相关参数对于地贫的筛查具有临床意义.
Analysis of Gene Mutation Types and Hematological Characteristics of Thalassemia in Xianning City
Objective To comprehensively understand the positive rate,mutation types,distribution characteristics,gender differences and hematology characteristics of thalassemia patients in the population of Xianning City through descriptive research.Methods A total of 3105 patients who underwent gene testing for thalassemia in our outpatient and inpatient clinics at our hospital were collected.EDTA anticoagulated blood was collected from all the sample population included in the study for routine blood tests.PCR-reverse dot hybridization was used to detect α and β thalassemia genes,and the sample genotype was determined by color development.Results Among the 3105 samples,223 patients were diagnosed with thalassemia by genetic testing for thalasse-mia,with a positive detection rate of 7.18%.Among them,32 were males and 191 were females,with no significant difference in gender distribution(χ2=0.189,P=0.663).Among the confirmed patients,125 cases were positive for β-thalassemia gene,ac-counting for 56.05%;95 cases were positive for β-thalassemia gene,accounting for 42.60%.Only 3 cases were positive for αβ-thalassemia gene,accounting for 1.35%.A total of 8 genotypes of α-thalassemia were detected in this study,the top ranked geno-type is-α3.7/αα,--SEA/αα and α4.2/αα,accounting for45.60%,37.60%,and9.60%respectivelyandaccounting for92.80%of all α-thalassemia gene carriers.A total of 11 genotypes of β-thalassemia were detected,with the top ranking being β654/βN,β41-42/βN and β17/βN,accounting for 43.16%,28.43%,and 9.47%respectively.Three cases of αβ-compound poverty were detectedwith genotypes as follows:-α3.7/αα&β41-42βN,--SEA/αα&β41-42/βN,-α4.2/αα&βIVS-Ⅱ-654/βN.The relevant he-matological indicators including hemoglobin(Hb),mean corpuscular volume(MCV),mean corpuscular hemoglobin(MCH),mean corpuscular hemoglobin concentration(MCHC)were compared among the normal group,α-thalassemia group,and β-thalassemia group,and the differences were statistically significant(P<0.05).Conclusion The positive detection rate and genotype of thalasse-mia in Xianning City are different from other areas in Hubei Province.Detecting of thalassemia genes can help improve the prevention and control of thalassemia in Xianning and guide eugenics and postnatal care.In addition,the red blood cell-related parameters in routine blood tests are clinically significant for the screening of thalassemia.

ThalassemiaGenetic mutationHematology parameters

葛仁英、熊婷、刘盼、邓福维

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咸宁市中心医院/湖北科技学院附属第一医院血液内科,湖北 咸宁 437100

地中海贫血 基因突变 血液学参数

2025

湖北科技学院学报(医学版)
湖北科技学院

湖北科技学院学报(医学版)

影响因子:0.5
ISSN:2095-4646
年,卷(期):2025.39(1)