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. 2004 Mar;57(3):276–280. doi: 10.1136/jcp.2003.008037

Table 5.

Haemoglobin A2 percentage, red cell indices, and haemoglobin S percentage in patients with sickle cell trait with or without α thalassaemia (the four patients with iron deficiency have been excluded)

α Gene status αα/αα (group A) −α/αα (group B) −α/−α (group C) Significance of difference
A v B B v C A v C
Hb (g/l) 125.1 (19.1) 114.9 (19.6) 119.5 (13.1) >0.1 >0.1 >0.1
RBC ×1012/l 4.48 (0.67) 4.45 (0.61) 5.54 (0.67) >0.1 <0.001 <0.001
MCV (fl) 84.88 (8.26) 79.08 (5.80) 67.77 (5.81) <0.001 <0.001 <0.001
MCH (pg) 28.05 (5.49) 25.79 (2.10) 21., 65 (1.84) <0.001 <0.001 <0.001
Hb S % by MC 37.24 (3.14) 32.61 (2.33) 25.53 (2.08) <0.001 <0.001 <0.001
Hb S % by HPLC 37.13 (2.51) 32.61 (1.91) 25.52 (1.44) <0.001 <0.001 <0.001
Hb A2 % by MC 3.23 (0.31) 3.41 (0.43) 3.54 (0.45) >0.1 >0.1 <0.01
Hb A2 % by SD 3.44 (0.62) 3.78 (0.7) 3.85 (0.72) >0.1 >0.1 <0.01
Hb A2 % by HPLC 4.33 (0.37) 4.41 (0.35) 4.49 (0.76) >0.1 >0.1 >0.1

A, subjects with no α gene deletion; B, subjects with one α gene deletion; C, subjects with two α gene deletions.

Values are mean (SD).

HPLC, high performance liquid chromatography; MC, microcolumn chromatography; MCH, mean cell haemoglobin; MCV, mean cell volume; RBC, red blood cells; SD, scanning densitometry.