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δ-β地中海贫血中珠蛋白合成的变异

Variations in globin synthesis in delta-beta-thalassaemia.

作者信息

Kinney T R, Friedman S, Cifuentes E, Kim H C, Schwartz E

出版信息

Br J Haematol. 1978 Jan;38(1):15-22. doi: 10.1111/j.1365-2141.1978.tb07103.x.

Abstract

Peripheral blood globin synthesis studies were done in 11 patients with delta beta-thalassaemia trait, Hb S-delta beta-thalassaemia or delta beta/betao-thalassaemia from two black and two Caucasian families. All patients had elevated Hb F and normal or decreased Hb A2 levels and 10 had family studies confirming the diagnosis. In addition, four unrelated non-thalassaemic patients with elevated Hb F levels also had peripheral blood globin synthesis studies. The beta/alpha specific activity globin synthesis ratios in the three blacks with delta beta-thalassaemia trait were 0.60--1.04. In the four Caucasians with delta beta-thalassaemia traint, the beta/alpha ratios were 0.58--1.02. These results demonstrate a wide range of ratios overlapping those of normal controls (0.99 +/- 0.06). The betas/alpha ratios in three blacks with Hb S-delta beta-thalassaemia ranged from 0.66 to 1.00, similar to those of patients with delta beta-thalassaemia trait. In the black patient with delta beta/betao-thalassaemia, the gamma/alpha ratio was 0.67. The beta/alpha peripheral blood ratios in the four non-thalassaemia patients with elevated Hb F ranged from 1.00 to 1.11, similar to those of normal controls. These studies indicate that a decreased beta/alpha ratio is not an invariable finding in delta beta-thalassaemia in blacks or Caucasian patients and that globin synthesis data alone is insufficient to diagnose definitively heterozygotes for delta beta-thalassaemia or to distinguish this trait from non-thalassaemic haematological disorders associated with a normal percentage of Hb A2 and an elevated level of Hb F.

摘要

对来自两个黑人家庭和两个白人家庭的11例δβ地中海贫血特征、Hb S-δβ地中海贫血或δβ/β0地中海贫血患者进行了外周血珠蛋白合成研究。所有患者的Hb F升高,Hb A2水平正常或降低,其中10例经家系研究确诊。此外,对4例Hb F水平升高的非地中海贫血无关患者也进行了外周血珠蛋白合成研究。3例具有δβ地中海贫血特征的黑人患者的β/α特异性活性珠蛋白合成比率为0.60--1.04。4例具有δβ地中海贫血特征的白人患者的β/α比率为0.58--1.02。这些结果表明,这些比率范围广泛,与正常对照组(0.99±0.06)的比率重叠。3例Hb S-δβ地中海贫血黑人患者的β/α比率在0.66至1.00之间,与具有δβ地中海贫血特征的患者相似。在患有δβ/β0地中海贫血的黑人患者中,γ/α比率为0.67。4例Hb F升高的非地中海贫血患者的外周血β/α比率在1.00至1.11之间,与正常对照组相似。这些研究表明,β/α比率降低在黑人或白人δβ地中海贫血患者中并非一成不变的发现,仅珠蛋白合成数据不足以明确诊断δβ地中海贫血杂合子,也不足以将该特征与Hb A2百分比正常且Hb F水平升高的非地中海贫血血液系统疾病区分开来。

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