Chien C C, Lin C K, Jiang M L, Wang C C, Lin J S
Department of Internal Medicine, Veterans General Hospital-Taipei, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1992 Oct;50(4):288-92.
The purpose of this survey is to find out whether Hakka group has higher incidence of thalassemia traits in our population. A total of 1,115 healthy employees from a company were screened by complete blood count (CBC) with indices. Those subjects with mean corpuscular volume (MCV) less than 80 fl were further evaluated by hemoglobin electrophoresis and modified hemoglobin H (Hb H) inclusion staining to confirm the diagnosis of beta- and alpha-thalassemia traits, respectively. We evaluated and compared the crude occurrence rates of thalassemia traits in Hakka, non-Hakka, and Taiwanese. Subjects with one or both Hakka parents had higher crude incidence of alpha-thalassemia traits than other groups of subjects, but this phenomenon wasn't found in beta-thalassemia traits.
本次调查的目的是了解在我们的人群中客家人群是否具有更高的地中海贫血特征发生率。对某公司的1115名健康员工进行了全血细胞计数(CBC)及相关指标检测。平均红细胞体积(MCV)小于80 fl的受试者进一步通过血红蛋白电泳和改良血红蛋白H(Hb H)包涵体染色进行评估,以分别确诊β地中海贫血特征和α地中海贫血特征。我们评估并比较了客家人、非客家人以及台湾人群中地中海贫血特征的粗发生率。父母一方或双方为客家人的受试者α地中海贫血特征的粗发生率高于其他受试者组,但β地中海贫血特征中未发现此现象。