Red cell deformability, splenic function and anaemia in thalassaemia

被引:38
作者
Dondorp, AM
Chotivanich, KT
Fucharoen, S
Silamut, K
Vreeken, J
Kager, PA
White, NJ
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Internal Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Div Infect Dis Trop Med & AIDS, NL-1105 AZ Amsterdam, Netherlands
[3] Mahidol Univ, Fac Trop Med, Bangkok, Thailand
[4] Mahidol Univ, Dept Med, Div Haematol, Inst Sci & Technol Res & Dev,Thalassaemia Res Ctr, Bangkok, Thailand
[5] John Radcliffe Hosp, Nuffield Dept Trop Med, Ctr Trop Med, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
thalassaemia; red cell deformability; anaemia; splenic function;
D O I
10.1111/j.1365-2141.1999.01367.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Red cell deformability (RCD) was measured in 38 patients with alpha-thalassaemia and 48 patients with beta-thalassaemia, of whom 13 had undergone splenectomy, All splenectomized patients, but none of those with intact spleens, had very rigid erythrocytes with an elongation index <0.45 at a high shear stress of 30 Pa suggesting a splenic recognition threshold for removal of rigid red cells, At this shear stress RCD correlated strongly with the degree of anaemia in both the splenectomized (r = 0.81, P < 0.001) and non-splenectomized beta-thalassaemic patients (all patients r = 0.81, P < 0.001; homozygous beta-thalassaemic patients r = 0.51, P = 0.01). These data suggest that reduced RCD is a major determinant of anaemia in thalassaemia.
引用
收藏
页码:505 / 508
页数:4
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