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巴勒斯坦加沙地带β-地中海贫血突变的频谱。

The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.

机构信息

Biology Department, Al Azhar University-Gaza, Gaza, Palestine.

出版信息

Blood Cells Mol Dis. 2013 Apr;50(4):247-51. doi: 10.1016/j.bcmd.2012.12.004. Epub 2013 Jan 12.

Abstract

BACKGROUND

β-Thalassemia is a disorder caused by mutations at the hemoglobin β-gene (HBB) locus. Its most important manifestation, the major form, is characterized by severe hypochromic and hemolytic anemia and is inherited in an autosomal recessive mode. In Gaza Strip, Palestine 0.02% of the population has been identified as β-thalassemia major.

DESIGN AND METHODS

An assessment of mutations was performed in 49 transfusion dependent patients with β-thalassemia major and in 176 β-thalassemia carriers diagnosed with a mean erythrocyte cell volume (MCV) <80fl and a proportion of HbA2>3.5%. In addition 39 individuals suspicious for β-thalassemia carrier status due to a reduced MCV (<80fl) but a normal HBA2 were screened.

RESULTS

By screening with three hybridization assays a proportion of 80% of the thalassemic chromosomes from patients and carriers was identified to carry five different mutations of the hemoglobin (Hb) β-gene. Subsequent DNA sequencing confirmed these and revealed further 9% of the chromosomes to be affected by other mutations. In addition six chromosomes from suspicious carriers were detected to carry β-thalassemia mutations. Of the 15 different HBB mutations identified the variant IVS-I-110 G>A was the most frequent mutation identified in 34% of the thalassemic chromosomes, followed by IVS-I-1 G>A, IVS-I-6 T>C, Codon 39 C>T, and Codon 37 G>A. Three novel HBB variants were discovered by direct sequencing of the gene: 5' UTR-50 (-/G), 5' UTR-43 C>T, and IVS-II-26 T>G.

CONCLUSIONS

The spectrum of HBB mutations described is of the Mediterranean type whereby the allele frequencies of the most common mutations differ from those, which were previously described for the population of the Gaza Strip and other Palestinian populations. The data presented may promote the introduction of molecular testing to the Palestinian premarital screening program for β-thalassemia in Gaza Strip, which will improve the screening protocol and genetic counseling in the future.

摘要

背景

β-地中海贫血症是一种由血红蛋白β基因(HBB)位点突变引起的疾病。其最重要的表现形式,即主要形式,特征为严重的低色素性和溶血性贫血,呈常染色体隐性遗传模式。在巴勒斯坦加沙地带,有 0.02%的人口被确定为β-地中海贫血主要患者。

设计和方法

在 49 名依赖输血的β-地中海贫血主要患者和 176 名β-地中海贫血携带者中进行了突变评估,这些携带者的平均红细胞体积(MCV)<80fl,且 HbA2 比例>3.5%。此外,还对 39 名因 MCV(<80fl)降低但 HBA2 正常而疑似β-地中海贫血携带者的个体进行了筛查。

结果

通过三种杂交检测,从患者和携带者中确定了 80%的地中海贫血染色体携带五个不同的血红蛋白(Hb)β基因突变。随后的 DNA 测序证实了这些突变,并发现另外 9%的染色体受到其他突变的影响。此外,还从疑似携带者的 6 条染色体中检测到β-地中海贫血突变。在所确定的 15 种不同的 HBB 突变中,变体 IVS-I-110 G>A 是最常见的突变,占地中海贫血染色体的 34%,其次是 IVS-I-1 G>A、IVS-I-6 T>C、Codon 39 C>T 和 Codon 37 G>A。通过直接测序基因,发现了三种新的 HBB 变体:5'UTR-50(-/G)、5'UTR-43 C>T 和 IVS-II-26 T>G。

结论

所描述的 HBB 突变谱为地中海类型,其中最常见突变的等位基因频率与之前描述的加沙地带和其他巴勒斯坦人群的频率不同。所提供的数据可能会促进将分子检测引入加沙地带的巴勒斯坦婚前筛查计划,以β-地中海贫血症,这将改善未来的筛查方案和遗传咨询。

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