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印度人群中β珠蛋白突变分析:罕见和新突变的存在及区域异质性

Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity.

作者信息

Edison E S, Shaji R V, Devi S G, Moses A, Viswabandhya A, Mathews V, George B, Srivastava A, Chandy M

机构信息

Department of Haematology, Christian Medical College, Vellore, Tamilnadu, India.

出版信息

Clin Genet. 2008 Apr;73(4):331-7. doi: 10.1111/j.1399-0004.2008.00973.x. Epub 2008 Feb 20.

Abstract

Beta thalassaemia is a major public health problem in India. A comprehensive database of the spectrum of mutations causing beta thalassaemia in the Indian population is necessary. This study in which a large number of patients with beta thalassaemia including those from certain regions that were not explored earlier shows a great heterogeneity of mutations. Several novel and rare alleles that have not been reported earlier in the Indian population have been identified, and mutations differ in frequency in different regions of the country. This information on the spectrum of mutations has implications for the control of beta thalassaemia in a population with complex ethnic background and also on the genotype-phenotype correlation of the disease.

摘要

β地中海贫血是印度一个主要的公共卫生问题。建立一个关于印度人群中导致β地中海贫血的突变谱的综合数据库很有必要。这项研究纳入了大量β地中海贫血患者,包括来自一些此前未被研究过的特定地区的患者,结果显示突变具有很大的异质性。已鉴定出一些此前在印度人群中未被报道过的新的罕见等位基因,且突变在该国不同地区的频率有所不同。这些关于突变谱的信息对于控制具有复杂种族背景人群中的β地中海贫血以及该疾病的基因型-表型相关性都具有重要意义。

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