Department of Laboratory Medicine, Pusan National University School of Medicine, Busan, Korea.
Department of BioMedical Informatics Unit, Pusan National University School of Medicine, Busan, Korea.
Ann Lab Med. 2019 Mar;39(2):133-140. doi: 10.3343/alm.2019.39.2.133.
Thalassemia is highly prevalent in Southeast Asia but is rare in Korea; however, Southeast Asian immigrant population is recently rising in Korea. We investigated the prevalence of thalassemia in Korea in the context of increasing immigration.
This prospective, observational, multicenter study was conducted between September 2015 and August 2017. A total of 669 subjects <30 years living in Korea were grouped into the multiethnic (N=314) and Korean (N=355) groups. Hb electrophoresis and complete blood count (CBC) were performed. If low mean corpuscular volume with high red blood cell distribution width coefficient of variation or a high fetal Hb (HbF) or Hb alpha 2 (HbA₂) level was observed, genetic testing of the α- and β-globin genes was performed. In addition, the number of potential thalassemia carriers in Korea was estimated by multiplying the prevalence of thalassemia in a specific ethnicity by the number of immigrants of that ethnicity.
Twenty-six multiethnic and 10 Korean subjects showed abnormal results for Hb electrophoresis and CBC. Eighteen multiethnic subjects and four Korean subjects were tested for α-globin and β-globin gene mutations. Within the multiethnic group, five subjects (1.5%) were α-thalassemia carriers, and six (1.9%) were β-thalassemia minor. The deletion in and , and c. 126_129delCTTT (p.Phe42Leufs*19) mutation of were the dominant inherited mutations.
The prevalence of thalassemia in young people in Korea is increasing due to the increasing number of Southeast Asian immigrants.
地中海贫血在东南亚地区高发,但在韩国罕见;然而,近年来东南亚移民数量在韩国不断增加。我们在移民增加的背景下调查了韩国地中海贫血的流行情况。
这是一项前瞻性、观察性、多中心研究,于 2015 年 9 月至 2017 年 8 月进行。共纳入 669 名居住在韩国、年龄<30 岁的受试者,分为多民族组(N=314)和韩国组(N=355)。进行血红蛋白电泳和全血细胞计数(CBC)检查。如果观察到低平均红细胞体积伴高红细胞分布宽度变异系数或高胎儿血红蛋白(HbF)或 Hb alpha 2(HbA₂)水平,则进行α-和β-珠蛋白基因的遗传检测。此外,通过特定族裔的地中海贫血患病率乘以该族裔的移民人数,估计韩国潜在地中海贫血携带者的数量。
26 名多民族和 10 名韩国受试者的血红蛋白电泳和 CBC 检查结果异常。18 名多民族和 4 名韩国受试者接受了α-和β-珠蛋白基因突变检测。在多民族组中,5 名受试者(1.5%)为α-地中海贫血携带者,6 名(1.9%)为β-地中海贫血轻度。主要遗传突变包括缺失和 ,以及 c.126_129delCTTT(p.Phe42Leufs*19)突变。
由于东南亚移民数量的增加,韩国年轻人中海地贫血的患病率正在上升。