节点文献

全自动高效液相色谱分析系统在地中海贫血诊断中的应用

Application of automated high-performance liquid chromatography in the diagnosis of thalassemia

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 夏超然王娟杨为群熊灿王伟

【Author】 XIA Chaoran;WANG Juan;YANG Weiqun;XIONG Can;WANG Wei;Shanghai Children’s Hospital,Institute for Medical Genetics,Shanghai Jiaotong University;Health Ministry Key Laboratory of Molecular Embryonic Biology,Shanghai Key Laboratory of Embryonic and Reproductive Engineering;Department of Hematology,Shanghai Children’s Hospital,Shanghai Jiaotong University;

【机构】 上海市儿童医院上海交通大学附属儿童医院上海交通大学医学遗传研究所卫生部医学胚胎分子生物学重点实验室 上海市胚胎与生殖工程重点实验室上海交通大学附属儿童医院血液科

【摘要】 目的探讨全自动高效液相色谱(HPLC)分析检测系统在地中海贫血(地贫)诊断和筛查中的临床应用价值。方法入选100例基因诊断确诊地贫患儿及35例正常儿童,应用HPLC检测系统以及传统碱变性法、醋纤电泳法定量分析HbF和HbA2;并比较不同检测方法与相应β地贫基因诊断结果的符合率、敏感性与特异性。结果β地贫74例,64例单杂合子,10例复合杂合子;α地贫26例,1例单杂合子,25例复合杂合子。在地贫患儿和正常儿童中,HPLC法测定的HbF百分含量均高于碱变性法,差异有统计学意义(P<0.01)。HPLC法测得的HbF在α地贫患儿和正常儿童间的差异亦有统计学意义(P=0.011),对α地贫的分辨力高于碱变性法。α地贫患儿,HPLC法测得的HbA2百分含量高于醋纤电泳法,差异有统计学意义(P=0.010);β地贫患儿,HPLC法和醋纤电泳法测得的单杂合子的HbA2含量均高于复合杂合子,差异有统计学意义(P<0.01)。HPLC方法测定HbF-HbA2(≥4.0%)联合MCV(<80 fl)、MCH(<27 pg),与α或β基因诊断的符合率达99.3%,灵敏度和特异度分别为99.0%和100.0%。结论采用HPLC法检测HbA2和HbF,并结合MCV、MCH,与基因诊断结果的符合率、灵敏度和特异度均高,可成为大规模筛查β地贫的一种理想方法。

【Abstract】 Objective To evaluate the application of high-performance liquid chromatography(HPLC) in diagnosis and screening of thalassemia. Methods Automated HPLC was used to measure HbF and HbA2 in 100 genetically diagnosed thalassemic patients and 35 normal children. The results were compared with those from traditional tests including alkali denaturation test and cellulose acetate electrophoresis. The diagnose accordance rates,sensitivity and specificity were compared. Results Seventy-four β thalassemia,64 were heterozygous with single mutations and 10 were compound heterozygous with double mutations. Twenty-six α thalassemia,25 were compound mutations and one was heterozygous with single mutation. The HbF percentage from HPLC was higher than that from alkali denaturation tests in either thalassemia or normal children(P<0.01). HbF level from HPLC in α-thalassemia was significantly different from that in the normal children(P=0.011). The percentage of HbA2 from HPLC was higher than that from cellulose acetate electrophoresis(P=0.010). HbA2 in the single heterozygous β-thalassemia were twice higher than that in the double heterozygous mutated β-thalassemia(P<0.01). The combination of HbF-HbA2(≥4.0%) from HPLC with MCV(<80 fl) and MCH(<27 pg) had high accordance rates(99.3%),sensitivity(99.0%) and specificity(100.0%) in diagnosis of thalassemia. Conclusions When the results of HPLC are combined with MCV and MCH,it can be applied to the diagnosis of thalassemia with high specificity,high sensitivity and has high diagnostic accordance rate with genetic results. HPLC can be an ideal approach to screen β thalassemia.

【基金】 国家科技支撑计划项目(No.2012BAI09B04)
  • 【文献出处】 临床儿科杂志 ,Journal of Clinical Pediatrics , 编辑部邮箱 ,2013年12期
  • 【分类号】R725.5
  • 【被引频次】12
  • 【下载频次】152
节点文献中: 

本文链接的文献网络图示:

本文的引文网络