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Updated: Mar 9, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
[Value of Analyzing Hemoglobin A2 by ROC Curve for Screening Thalassemia]
Tian-Wen He1, Li-Hua Yu1, Hao Guo1
1Medical Genetics Center, Key Laboratory of Metabolic and Genetic Diseases of Women and Children,Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Objective:
To investigate the value of hemoglobin A2(HbA2) for screening thalassemia.
Methods:
A total of 2 000 adults' peripheral blood samples from Guangdong Women and Children Hospital from June 2013 to January 2014 were collected. The hemoglobin A2 (HbA2) level was analyzed by the full automatic capillary electrophoresis technique, and the genotypes of thalassemia were detected.
Results:
The optimal cutoff values of HbA2 for screening silent α-thalassemia, α-thalassemia trait, intermedia α-thalassemia and β-thalassemia trait were 2.85%, 2.65%, 2.25% and 3.45%, respectively; the areas under receiver operator characteristic (ROC) curve were 0.709, 0.839, 0.979 and 0.997 respectively; the sensitivities were 0.481, 0.721, 0.953 and 0.994, and the specificities were 0.846, 0.837, 0.929 and 0.969 respectively.
Conclusion:
The optimal cutoff values of HbA2 for screening different type of thalassemia based on our laboratory data are established by using ROC curve. According to the area under ROC curve, a satisfactory accuracy for screening intermedia α-thalassemia and β-thalassemia trait can be achieved by detecting hemoglobin A2 level.
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