The role of haemoglobin A2 testing in the diagnosis of thalassaemias and related haemoglobinopathies

被引:136
作者
Mosca, A. [1 ,2 ]
Paleari, R. [1 ,2 ]
Ivaldi, G. [3 ]
Galanello, R. [4 ]
Giordano, P. C. [5 ]
机构
[1] Univ Milan, Dept Sci & Biomed Technol, I-20090 Milan, Italy
[2] Univ Milan, Ctr Metrol Traceabil Lab Med, CIRME, I-20090 Milan, Italy
[3] Osped Galliera, Lab Human Genet & Microcitaemias, Genoa, Italy
[4] Univ Cagliari, Hematol Lab, Osped Reg Microcitemie ASL8, Cagliari, Italy
[5] Leiden Univ, Med Ctr, Dept Human & Clin Genet, Haemoglobinopathies Lab, Leiden, Netherlands
关键词
BETA; ELECTROPHORESIS; BLOOD; TRAIT; A2;
D O I
10.1136/jcp.2008.056945
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The increase in haemoglobin (Hb)A(2) level is the most significant parameter in the identification of beta thalassaemia carriers. However, in some cases the level of HbA(2) is not typically elevated and some difficulties may arise in making the diagnosis. For these reasons the quantification of HbA(2) has to be performed with great accuracy and the results must be interpreted together with other haematological and biochemical evidence. The present document includes comments on the need for accuracy and standardisation, and on the interpretation of the HbA(2) value, reviewing the most crucial aspects related to this test. A practical flow-chart is presented to summarise the significance of HbA(2) estimation in different thalassaemia syndromes and related haemoglobinopathies.
引用
收藏
页码:13 / 17
页数:5
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