Vyas P, Higgs D R, Weatherall D J, Dunn D, Serjeant B E, Serjeant G R
Medical Research Council Laboratories, University of the West Indies, Kingston, Jamaica.
Br J Haematol. 1988 Dec;70(4):449-54. doi: 10.1111/j.1365-2141.1988.tb02515.x.
The effects of alpha thalassaemia on sickle cell-beta zero thalassaemia have been studied by comparing haematological and clinical features in four subjects homozygous for alpha thalassaemia 2 (2-gene group), 27 heterozygotes (3-gene group), and 55 with a normal alpha globin gene complement (4-gene group). Alpha thalassaemia was associated with significantly higher haemoglobin levels and lower reticulocyte counts independent of the presence of splenomegaly. Contrary to expectation, alpha thalassaemia was associated with small but significant increases in mean cell volume and mean corpuscular haemoglobin concentration. Splenomegaly at age 5 years and episodes of acute splenic sequestration were significantly more frequent in the 4-gene group. There were no significant differences in painful crises, acute chest syndrome, or other clinical features.
通过比较4名α地中海贫血2纯合子(2基因组)、27名杂合子(3基因组)和55名具有正常α珠蛋白基因互补的个体(4基因组)的血液学和临床特征,研究了α地中海贫血对镰状细胞-β0地中海贫血的影响。α地中海贫血与显著更高的血红蛋白水平和更低的网织红细胞计数相关,且与脾肿大的存在无关。与预期相反,α地中海贫血与平均红细胞体积和平均红细胞血红蛋白浓度的小幅但显著增加有关。4基因组在5岁时脾肿大和急性脾滞留发作明显更频繁。在疼痛性危机、急性胸部综合征或其他临床特征方面没有显著差异。