Winichagoon P, Fucharoen S, Wilairat P, Fukumaki Y
Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:235-40.
Hemoglobinopathies are the most common genetic disorders in Southeast Asia. alpha-Thalassemia is most often due to a alpha-globin gene deletion. Hb Constant Spring (CS) occurs from the mutation at the termination codon of the alpha-globin gene resulting in an elongated polypeptide; alpha(CS)-globin mRNA is also unstable and only small amounts of Hb CS are produced. Thus Hb CS has an alpha-thalassemia 2-like effect. beta-Thalassemia results from a variety of molecular mechanisms, most of which are single base substitutions or deletions or insertions of one to four nucleotides. Hemoglobin E occurs from a Glu --> Lys substitution at position 26 of the beta-globin chain. The abnormal gene also results in reduced amounts of beta E-mRNA and hence of beta E-globin chains. Therefore, Hb E has a mild beta + thalassemia phenotype. Homozygous beta-thalassemia and beta-thalassemia/Hb E are the major beta-thalassemic syndromes in Southeast Asia. In spite of seemingly identical genotypes, severity of beta-thalassemia/Hb E patients can vary greatly. Some may have a severe clinical disorder approaching that seen in homozygous beta-thalassemia. A number of genetic factors have been shown to determine the differences in severity of anemia in beta-thalassemia/Hb E, including co-inheritance of alpha-thalassemia determinants and co-inheritance of other determinants which elevate Hb F expression. A correlation between the extent of beta E-globin mRNA cryptic splicing and the severity of anemia in beta(zero)-thalassemia/Hb E patients has been observed. Complete characterization of mutations causing hemoglobinopathies will help to bolster the establishment of prenatal diagnosis of these genetic disorders in the region.
血红蛋白病是东南亚最常见的遗传性疾病。α地中海贫血最常见的原因是α珠蛋白基因缺失。血红蛋白恒河猴(Hb Constant Spring,简称Hb CS)是由α珠蛋白基因终止密码子突变导致多肽链延长而产生的;α(CS)-珠蛋白mRNA也不稳定,仅产生少量的Hb CS。因此,Hb CS具有类似α地中海贫血2的效应。β地中海贫血由多种分子机制引起,其中大多数是单碱基替换、一至四个核苷酸的缺失或插入。血红蛋白E(Hb E)是由β珠蛋白链第26位的谷氨酸(Glu)被赖氨酸(Lys)取代所致。异常基因还导致βE-珠蛋白mRNA数量减少,进而βE-珠蛋白链数量减少。因此,Hb E具有轻度β+地中海贫血表型。纯合子β地中海贫血和β地中海贫血/Hb E是东南亚主要的β地中海贫血综合征。尽管基因型看似相同,但β地中海贫血/Hb E患者的严重程度差异很大。一些患者可能患有严重的临床疾病,接近纯合子β地中海贫血患者的情况。已证明一些遗传因素可决定β地中海贫血/Hb E患者贫血严重程度的差异,包括α地中海贫血决定因素的共同遗传以及其他提高Hb F表达的决定因素的共同遗传。已观察到β(0)-地中海贫血/Hb E患者中βE-珠蛋白mRNA隐匿性剪接程度与贫血严重程度之间存在相关性。对导致血红蛋白病的突变进行全面表征将有助于加强该地区这些遗传性疾病的产前诊断。