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Increased Prevalence of Thalassemia in Young People in Korea: Impact of Increasing Immigration

BACKGROUND: 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. METHODS: This prospective, observational, mu...

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Detalles Bibliográficos
Autores principales: Lee, Hyun-Ji, Shin, Kyung-Hwa, Kim, Hyung-Hoi, Yang, Eu Jeen, Park, Kyung-Hee, Kim, Min Ju, Kwon, Jeong-Ran, Choi, Young-Sil, Kim, Jun Nyun, Shin, Myung-Geun, Cho, Yong Gon, Kim, Sun Jun, Kim, Kyeong-Hee, Jeong, Seri, Kong, Seom Gim, Jung, Yu Jin, Lee, Nayoung, Kim, Man Jin, Seong, Moon-Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240526/
https://www.ncbi.nlm.nih.gov/pubmed/30430775
http://dx.doi.org/10.3343/alm.2019.39.2.133
Descripción
Sumario:BACKGROUND: 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. METHODS: 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 (HbA(2)) 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. RESULTS: 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 SEA deletion in HBA1 and HBA2, and c. 126_129delCTTT (p.Phe42Leufs*19) mutation of HBB were the dominant inherited mutations. CONCLUSIONS: The prevalence of thalassemia in young people in Korea is increasing due to the increasing number of Southeast Asian immigrants.