| Literature DB >> 28413893 |
Prapapun Leckngam1, Ektong Limweeraprajak2, Tiemjan Kiewkarnkha3, Thanusak Tatu1.
Abstract
Identifying double heterozygosities in Hb E (HBB: c.79 G>A)/- -SEA (Southeast Asian) (α-thalassemia-1) (α-thal-1) in patients first diagnosed as carrying Hb E is important in thalassemia control. Low Hb E, mean corpuscular volume (MCV) and mean corpuscular hemoglobin (Hb) (MCH) levels have been observed in this double heterozygosity. However, the cutoff points of these parameters have never been systematically established. Here, we analyzed Hb E and red blood cell (RBC) parameters in 372 Hb E patients grouped by Hb levels, by the status of - -SEA and -α3.7 (α-thal-2; rightward) deletions, to establish the cutoff points. Then, the established cutoff points were evaluated in 184 Hb E patients. It was found that the cutoff points of Hb E, MCV, MCH were significantly dependent on the Hb levels. In the group having Hb levels <10.0 g/dL, the cutoff points of Hb E, MCV and MCH were 21.2%, 64.9 fL and 21.0 pg, respectively, and were 25.6%, 72.8 fL and 23.9 pg, respectively, in the group having Hb levels 10.0-11.9 g/dL. Finally, in the group having Hb levels ≥12.0 g/dL, the cutoff points of Hb E, MCV and MCH were 27.1%, 76.7 fL and 25.3 pg, respectively. Thus, to screen for the double heterozygous Hb E/- -SEA anomaly in patients initially diagnosed as carrying Hb E, the Hb levels must be taken into account in choosing the suitable cutoff points of these three parameters.Entities:
Keywords: Anemia; Hb E level; double heterozygosity for Hb E/––SEA α-thal-1; heterozygous Hb E; total Hb levels
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Year: 2017 PMID: 28413893 DOI: 10.1080/03630269.2017.1295984
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849