期刊文献+

Hb、MCV、MCH在腾冲汉族地贫筛查中的临床应用价值 被引量:8

Clinical application value of Hb,MCV and MCH in thalassemia screening in Han ethnicity at Tengchong
下载PDF
导出
摘要 目的探讨血液学参数血红蛋白浓度(Hb)、平均红细胞体积(MCV)、红细胞平均血红蛋白含量(MCH)在腾冲市汉族人群缺失型α-地中海贫血和常见突变型β-地中海贫血筛查中的临床应用价值,研究临床初筛方案。方法随机选择2017年12月在腾冲市人民医院检验科进行常规体检的500例汉族受试者进行血常规检测,通过基因诊断确诊为常见的缺失型α-地中海贫血和突变型β-地中海贫血,比较Hb、MCV、MCH单项及联合检测对地中海贫血筛查的灵敏度和特异度,探讨其临床应用价值,制定适合当地人群的临床筛查截断值。结果腾冲市汉族中最常见的α-和β-地中海贫血分别为-α3.7/αα和异常血红蛋白E(HbE),血液学参数MCH、MCV分别为筛查-α3.7/αα及HbE筛查最具价值的指标。结论血液学参数Hb、MCV、MCH对腾冲市汉族人群上述2种常见地中海贫血的筛查有临床应用价值。 Objective To explore the clinical effects of hematological characteristics of hemoglobin concentration (Hb),mean corpuscular volume (MCV),and mean corpuscular hemoglobin content (MCH) in screening common deletional α-thalassemia and mutant β-thalassemia in Han ethnicity at Tengchong and study the clinical screening projects. Methods A total of 500 subjects of Han ethnicity who underwent routine physical examination in the Department of Clinical Laboratory of the People′s Hospital of Tengchong in December 2017 were randomly selected for routine blood test,and the common deleted alpha-thalassemia and mutant beta-thalassemia were diagnosed by gene diagnosis.The sensitivity and specificity of Hb,MCV and MCH for screening thalassemia were compared in order to explore its clinical application value and to establish the cut-off value of clinical screening suitable for local population. Results The common genotype of α-thalassemia and β-thalassemia in Han ethnicity in Tengchong city were-α 3.7 /αα and abnormal hemoglobin E (HbE) respectively.MCH and MCV analysis were the most valuable indicators for screening-α 3.7 /αα and HbE respectively. Conclusion Hematological characteristics of Hb,MCV and MCH have application value for screening common deletional α-thalassemia and mutant β-thalassemia in Han ethnicity at Tengchong.
作者 李冬 李开龙 易浩安 李宏 江伟阳 何永蜀 LI Dong;LI Kailong;YI Haoan;LI Hong;JIANG Weiyang;HE Yongshu(Department of Clinical Laboratory,the People′s Hospital of Tengchong,Tengchong,Yunnan 679100,China;Department of Cell Biology and Medical Genetics,Kunming Medical University,Kunming,Yunnan 650500,China)
出处 《国际检验医学杂志》 CAS 2019年第12期1417-1420,共4页 International Journal of Laboratory Medicine
基金 国家自然科学基金项目(31760308)
关键词 地中海贫血 血红蛋白 平均红细胞体积 红细胞平均血红蛋白含量 thalassemia hemoglobin mean corpuscular volume mean corpuscular hemoglobin content
  • 相关文献

参考文献8

二级参考文献41

  • 1张新华,李平萍,罗瑞贵,黄蒙莎,兰小英,吴志奎,王荣新.高效液相色谱法定量分析HbA_2在珠蛋白生成障碍性贫血筛查中的应用[J].临床检验杂志,2007,25(3):172-173. 被引量:11
  • 2Calanello R, Cao A. Alpha-thalassemia [J]. Cenet Med, 2011, 13: 83-88.
  • 3KOHNE E. Hemoglobinopathies:clinical manifestations, diagnosis, and treatment[J]. Dtsch Arztebl Int, 2011, 108:532-540.
  • 4张伯红,王申五,王黎明.广西地区新生儿脐血α-地贫的筛查和基因分析[J].中国医学科学院学报,1986,12(3):81-82.
  • 5WAJCMAN H,MORADKHANI K.Abnormal haemoglobins:detection&characterization[J].Indian J Med Res,2011(134):538-546.
  • 6LI TK,LEUNG KY,LAM YH,et al.Haemoglobin level,proportion of haemoglobin Bart's and haemoglobin Portland in fetuses affected by homozygousα0-thalassemia from 12 to 40 weeks'gestation[J].Prenat Diagn,2010,30(12-13):1126-1130.
  • 7OU Z1,LI Q,LIU W,et al.Elevated hemoglobin A2 as a marker forβ-thalassemia trait in pregnant women[J].Tohoku J Exp Med,2011,223(3):223-226.
  • 8LIAO C,YANG X,LI FT,et al.The detection of aneuploidy and maternal contamination by QF-PCR in samples undergoing prenatal diagnosis for thalassemia in Southern China[J].Eur J Obstet Gynecol Reprod Biol,2009,144(2):149-152.
  • 9YIN A,LI B,LUO M,et al.The prevalence and molecular spectrum ofα-andβ-globin gene mutations in 14,332 families of Guangdong Province,China[J].PLo S One,2014,9(2):89855.
  • 10周建中.缺铁性贫血的血象改变[J].中国现代药物应用,2008,2(1):34-36. 被引量:7

共引文献237

同被引文献69

引证文献8

二级引证文献26

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部