Lin C K, Lee S H, Wang C C, Jiang M L, Hsu H C
Department of Medicine, Veterans General Hospital, Taipei, Taiwan, Republic of China.
J Lab Clin Med. 1991 Dec;118(6):599-603.
The aim of this study was to determine the crude prevalence of alpha-thalassemia traits in Taiwan. A total of 1435 healthy employees from a statewide company were randomly screened by complete blood count determination with indices. Subjects with mean corpuscular volume less than 80 fl were analyzed by hemoglobin electrophoresis on cellulose acetate to exclude beta-thalassemia and with serum ferritin to exclude iron deficiency. Modified hemoglobin H inclusion staining was performed to confirm the diagnosis of alpha-thalassemia traits, and DNA probe studies were used to confirm the validity of this test. The overall prevalence rate of alpha-thalassemia trait was 3.4% (48 out of 1435). In persons of mainland Chinese origin, prevalence was 0.4%, and among persons of Taiwanese origin, it was 4.0% (47 out of 1171). We conclude that alpha-thalassemia traits are common genetic disorders in Taiwan and that antenatal screening is advised to reduce the frequency of occurrence of hemoglobin Bart's hydrops fetalis. The methods we used proved to be reliable and inexpensive.
本研究的目的是确定台湾地区α地中海贫血特征的粗略患病率。从一家全州性公司随机抽取了1435名健康员工,通过全血细胞计数及各项指标进行筛查。平均红细胞体积小于80 fl的受试者通过醋酸纤维素血红蛋白电泳分析以排除β地中海贫血,并检测血清铁蛋白以排除缺铁性贫血。采用改良的血红蛋白H包涵体染色来确诊α地中海贫血特征,并使用DNA探针研究来证实该检测的有效性。α地中海贫血特征的总体患病率为3.4%(1435人中48人)。在中国大陆祖籍人群中,患病率为0.4%,在台湾祖籍人群中,患病率为4.0%(1171人中47人)。我们得出结论,α地中海贫血特征在台湾是常见的遗传性疾病,建议进行产前筛查以降低血红蛋白Bart水肿胎儿的发生频率。我们所采用的方法被证明是可靠且经济的。