撒丁岛居民δ + 27型地中海贫血的发病率。

Clinical and laboratory haematology Pub Date : 1996-12-01
L Guiso, L Frogheri, P Pistidda, L Angioni, F Dore, S Pardini, M Longinotti
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引用次数: 0

摘要

为了确定北撒丁岛δ + 27地中海贫血的发病率,我们采用基于聚合酶链反应的分子分析方法检测了750名撒丁岛男生的血液样本。本研究中δ + 27突变的发生率为1.2%,是以往表型研究的两倍;地中海贫血的发生率为10.5%,其相互作用计算为0.0003。大多数δ + 27携带者的HbA2水平低于1.9%,其平均HbA2水平明显低于正常人。δ + 27和β -地中海贫血的所有复合杂合子均表现出与其HbA2水平正常化相关的沉默型β -地中海贫血表型。这项研究表明,在为有风险的夫妇提供咨询时,应牢记delta+ 27地中海贫血,其中一方具有典型的高HbA2 β -thal特征,而另一方显示正常或边缘HbA2水平。在这些受试者中,基于pcr的ECO O 109 I消化δ珠蛋白基因可以快速检测δ + 27突变。
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Frequency of delta+ 27-thalassaemia in Sardinians.

To determine the incidence of delta+ 27 thalassaemia in Northern Sardinia we examined blood samples from 750 Sardinian schoolboys by PCR-based molecular analysis. The incidence of delta+ 27 mutation was 1.2% in this study, i.e. twice as high as previously described on the basis of phenotypical studies; the frequency of the beta-thalassaemia is 10.5% and their interaction has been calculated at 0.0003. The majority of delta+ 27 carriers are characterized by a HbA2 level lower than 1.9% and the mean HbA2 level is significantly lower than in normal subjects. All compound heterozygotes for delta+ 27 and beta-thalassaemia show a silent beta-thalassaemic phenotype related to normalization of their HbA2 levels. This study suggests that delta+ 27 thalassaemia should be borne in mind in counselling at-risk couples in which one member has the typical high HbA2 beta-thal trait while the other shows normal or borderline HbA2 level. In these subjects, PCR-based ECO O 109 I digestion of the delta globin gene allows rapid detection of the delta+ 27 mutation.

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