학술논문
Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system.
Document Type
Article
Source
Subject
*THALASSEMIA diagnosis
*BETA-Thalassemia
*AUTOANALYZERS
*HYDROPS fetalis
*CARRIER state (Communicable diseases)
*ANALYTICAL chemistry techniques
*COMMERCIAL product evaluation
*CORD blood
*HEMOGLOBINS
*THAI people
*THALASSEMIA
*EVALUATION research
*DESCRIPTIVE statistics
*GENOTYPES
*EVALUATION
*DIAGNOSIS
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Language
ISSN
1751-5521
Abstract
Introduction We have evaluated an automated capillary isoelectric focusing ( cIEF)-based Hb analyzer in diagnosis of hemoglobinopathies commonly found among South East Asian population. Methods Study was performed on a cohort of 665 adult Thai subjects and 13 fetal blood specimens obtained at routine thalassemia diagnostic laboratory. Hb analysis was performed using the cIEF system. Thalassemia genotypes were defined by DNA analysis. Results The system revealed satisfactorily within-run and between-run precision for quantitation of Hb A2 and Hb E ( CV: 0.02-0.09%). The reference ranges of Hb A2 and Hb E were 2.6-4.0% and 25.7-33.1%, respectively. The system identified the cases of β-thalassemia and Hb E disorders correctly. Several thalassemia genotypes and Hb variants were identifiable. However, Hb Constant Spring was separated closely to Hb A2 and Hbs Bart's and H were relatively difficult to be reported due to interfering peaks separating at the same regions. Prenatal diagnosis by fetal blood analysis was found to be accurate for Hb Bart's hydrops fetalis and Hb E-β0-thalassemia disease. Conclusions The cIEF system could accurately diagnose β-thalassemia and Hb E carriers and demonstrate many Hb variants found in the region. The system cannot report Hb A2 in the presence of Hb E whereas Hbs Lepore and F are comigrated. Diagnosis of α-thalassemia disease based on Hb H and Hb Bart's might be difficult. [ABSTRACT FROM AUTHOR]