潮州地区人群血红蛋白病基因型分布调查  

Clinical and molecular characters of hemoglobinopathy in Chaozhou population

作　　者：林芬[1] 林春萍[1] 翁妙珊[1] 杨惠钿[1] 林敏[1] 杨立业[1] 

机构地区：[1]南方医科大学附属潮州中心医院检验实验中心,广东潮州521021

出　　处：《分子诊断与治疗杂志》2012年第2期107-110,共4页Journal of Molecular Diagnostics and Therapy

基　　金：国家自然科学基金(81101329);广东省医学科研基金(A2011758;B2010348;A2009781);潮州市社会发展计划(2009S14)

摘　　要：目的了解潮州地区人群血红蛋白病的分布状况和基因型。方法采用血细胞平均体积(MCV)、红细胞脆性及血红蛋白电泳3种方法联合检测,对本地区人群(2936例)进行血红蛋白病的筛查。筛查阳性样本采用跨越断裂点多聚酶链反应(gap-PCR)和反向斑点杂点(reverse dot blot)技术进行地贫基因确诊,以PCR-DNA测序法进行异常血红蛋白(除Hb E)突变的鉴定。结果潮州地区人群的筛查阳性率为9.43%(277/2936)。其中164例接受地贫基因诊断,诊断率为59.21%(164/277)。在115例确诊为地中海贫血的样本中,α-地贫占78.26%(90/115),以东南亚缺失型(--SEA)为主;β-地贫占21.74%(25/115),其中654M位点突变发病率最高,其次是41-42M;异常血红蛋白携带者6例,为Hb Q-Thailand、Hb K-NewYork、Hb J-Bangkok、Hb G-Chinese各1例,Hb E 2例。结论潮州地区人群地中海贫血发病率较高,以α-地中海贫血居多。本研究结果对于开展遗传咨询、产前诊断具有重要的参考价值。Objective To investigate the genotype distribution of hemoglobinopathy（thalassemia and abnormal hemoglobin） in Chaozhou population. Methods A total of 2396 samples were screened for hemoglobinopathy by combined MCV, erythrocyte fragility tests and hemoglobin electrophoresis. Thalassemia genotypes were identified by Gap-PCR and Reverse Dot Blot. The mutants of globin gene were detected by PCR- DNA sequencing. Rusults The positive screening rate was 9.43%（277/2936） in Chaozhou population. 164 cases of these 277 people received thalassemia genotype diagnosis and diagnostic rate was 59.21%（164/277）. 115 people were positive for thalassemia molecular diagnosis. The rate of α-thalassemia was 78.26%（90/115） and the major part of them was --SEA. The rate of β -thalassemia was 21.74%（25/115） and the major genotype of β -thalassemia was 654M, followed by 41-42M. 6 cases of abnormal hemoglobin were found, which included a case of Hb Q-Thailand, a case of Hb K-NewYork, a case of Hb J-Bangkok, a case of Hb G-Chinese and two cases of HbE. Conclusion There was a high prevalence of hemoglobinopathy with the majority of α -thalassemia in Chaozhou population. There was reference value of our investigation for genetic counseling and prenatal diagnosis.

关 键 词：筛查 地中海贫血 异常血红蛋白 基因诊断 

分 类 号：R556[医药卫生—血液循环系统疾病]