Department of Medicine, Faculty of Medicine, University of Kelaniya, Ragama, Sri Lanka.
Hemoglobin. 2022 Jan;46(1):71-73. doi: 10.1080/03630269.2022.2025826.
The island nation of Sri Lanka with 22 million people (in 2020) has an estimated 2000 patients with severe thalassemia. The majority have β-thalassemia (β-thal) major (β-TM), and Hb E (: c.79G>A)/β-thal accounts for most of the remainder. Carrier rate for α-thalassemia (α-thal) trait is 9.9% and β-thal trait is 2.5%, with very similar rates in the three major ethnic groups (Sinhalese, Tamils and Moors). The distribution of thalassemia type reveals a remarkable variation, even in this small island, mirroring historical distribution of malaria. Even though healthcare is provided free by the state including blood transfusions and chelation, the overall survival of patients of β-TM is still not on a par with that of the Mediterranean countries. A national thalassemia prevention program was set up in 2007, but overall success of the exercise based essentially on dissuasion of marriages is not very promising.
斯里兰卡是一个拥有 2200 万人口(2020 年数据)的岛国,估计有 2000 名重型地中海贫血症患者。大多数患者为β-地中海贫血症(β-TM),而 Hb E(: c.79G>A)/β-地中海贫血症占大多数。α-地中海贫血症(α-thal)携带者的发生率为 9.9%,β-地中海贫血症携带者的发生率为 2.5%,在三大主要族群(僧伽罗人、泰米尔人和摩尔人)中,这一比率非常相似。地中海贫血症类型的分布差异显著,即使在这个小岛上,也反映了疟疾的历史分布。尽管国家提供包括输血和螯合在内的免费医疗,但β-TM 患者的整体存活率仍无法与地中海国家相媲美。2007 年,该国建立了地中海贫血症预防计划,但该计划的主要目的是劝阻婚姻,基于劝阻婚姻的地中海贫血症预防计划整体成功率并不乐观。