血管性血友病因子血浆浓度的遗传学研究。

K H Orstavik
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引用次数: 0

摘要

在没有出血性疾病的个体中,血管性血友病因子(vWf)的血浆浓度变化范围很广。在一项双胞胎研究中,我们发现60%的vWf血浆浓度差异是由遗传因素引起的。AB0血型的个体比a、B或AB血型的个体有更低的vWf浓度。30%的遗传变异是由于AB0位点的影响。由于Lewis物质与ABH血型物质具有很大的结构相似性,我们比较了红细胞表面有Lea抗原和没有Lea抗原的个体的vWf浓度。缺乏Lea抗原的个体的vWf浓度低于具有该抗原的个体。Le(a+b-)人是非分泌者,Le(a-b+)人是ABH物质的分泌者。vWf浓度最低的是血组0。AB0基因座和分泌基因座可能是决定vWf血浆浓度的主要基因座。
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Genetics of plasma concentration of von Willebrand factor.

The plasma concentration of von Willebrand factor (vWf) shows a very wide range in individuals without bleeding disorders. In a twin study we found that 60% of the variance of the plasma concentration of vWf is due to genetic factors. Individuals with AB0 blood group 0 have a lower concentration of vWf than individuals with blood group A, B or AB. Thirty percent of the genetic variance was due to an effect of the AB0 locus. Since the Lewis substances show great structural similarity to the ABH blood group substances we compared the vWf concentration in individuals with and without the Lea antigen on the red cell surface. Individuals lacking the Lea antigen had a lower vWf concentration than individuals who had this antigen. Le(a+b-) people are nonsecretors and Le(a-b+) people are secretors of ABH substance. The lowest vWf concentration was found in blood group 0 secretors. Both the AB0 locus and the Secretor locus may be major loci for the determination of the plasma concentration of vWf.

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