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三亚市儿童地中海贫血筛查及基因分析

  • 周祥敏 ,
  • 陈垂婉 ,
  • 陈垂海 ,
  • 霍开明 ,
  • 陈爱华 ,
  • 陈求珠 ,
  • 陈垂任
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  • 1. 三亚市妇幼保健院儿科和检验科( 海南三亚 572000);2. 海南省农垦总医院儿科( 海南海口 570311)

收稿日期: 2015-08-15

  网络出版日期: 2015-08-15

Screening and genetic diagnosis of childhood thalassemia in Sanya city 

  • ZHOU Xiangmin ,
  • CHEN Chuiwan ,
  • CHEN Chuihai ,
  • HUO Kaiming ,
  • CHEN Aihua ,
  • CHEN Qiuzhu ,
  • CHEN Chuiren
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  • 1. Department of Pediatrics and Laboratory,Sanya Maternity and Child Health Hospital, Haikou 572000, Hainan China; 2. Hainan Agricultural Reclamation General Hospital of Pediatrics, Haikou 570311, Hainan China

Received date: 2015-08-15

  Online published: 2015-08-15

摘要

目的 调查三亚市儿童地中海贫血的发病率和基因突变类型。方法 对938例儿童进行血常规、CRP检测和血红蛋白电泳试验,筛查地中海贫血发生情况及其所属类型;对α-地中海贫血患儿用gap-PCR法、β-地中海贫血患儿用PCR-RDB法进行基因诊断。结果 地中海贫血筛查阳性率为13.65%(128/938),基因诊断阳性率为11.41%(107/938)。在107例经基因诊断确诊为地中海贫血的患儿中,α-地中海贫血59例,β-地中海贫血46例,α合并β地中海贫血2例。59例α-地中海贫血患儿中,-SEA/αα型31例,-α4.2/αα型13例,HbH病为6例;46例β-地中海贫血患儿中共检出6个基因位点发生突变,突变频率依次为CD41-42(-CTTT)21例,TATAbox-28(A→G)13例,CDs14/15(+G)5例,IVS-Int 654(C→T)4例,CD17(A→T)2例,27-28(+C)1例。结论 三亚市儿童地中海贫血发病率较高,开展遗传咨询、婚前检查及产前诊断等对优生优育十分必要。

本文引用格式

周祥敏 , 陈垂婉 , 陈垂海 , 霍开明 , 陈爱华 , 陈求珠 , 陈垂任 . 三亚市儿童地中海贫血筛查及基因分析[J]. 临床儿科杂志, 2015 , 33(8) : 726 . DOI: 10.3969 j.issn.1000-3606.2015.08.011

Abstract

 Objective To investigate the incidence and gene mutation spectrum of childhood thalassemia in Sanya city. Methods There were 938 children in our hospital screened by routine blood test, C-reactive protein test and hemoglobinelectrophoresis. Based on the screening results in children with thalassemia and its subtypes, the alpha thalassaemia children were diagnosed by gap - polymerase chain reaction, while the beta thalassaemia ones were diagnosed by polymerase chain reaction-reverse dot blot, and all the results were retrospectively analyzed. Results Screening positive rate of thalassemia anemia was 13.65% (128/938), genetic diagnosis positive rate was 11.41% (107/938). In 107 cases diagnosed with thalassemia by genetic test, 59 were alpha thalassaemia, and 46 were beta thalassaemia, and 2 cases were alpha thalassaemia combined with beta thalassaemia. In 59 cases of alpha thalassaemia, 31 had genotype of - SEA/alpha alpha , 13 cases with genotype alpha 4.2 / alpha alpha, and 6 were of HbH disease. In the 46 cases of beta thalassaemia children, six gene locus mutations were found : CD41-42 (CTTT) in 21 cases, TATAbox - 28 (A - G) in 13 cases, CDs14/15 (G) in 5 cases, IVS - Int 654 (C - > T) in 4 cases, CD17 (A - > T) in 2 cases, and 27-28 (C) in 1 case. Conclusion High prevalence of thalassemia in children from Sanya city warrants genetic counseling, premarital check-up and prenatal diagnosis.
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