Thalassemia and Sickle Cell Society, Raghavendra Colony, Rajendra Nagar, Rangareddy District, Hyderabad, Telangana State, India.
Genome Foundation, Banjara Hills, Hyderabad, Telangana State, India.
Hemoglobin. 2020 Sep;44(5):371-375. doi: 10.1080/03630269.2020.1814805. Epub 2020 Oct 2.
The burden of β-thalassemia (β-thal) is largely underestimated in India with a carrier frequency of 3.0-4.0% in general, whereas highly stratified frequencies of up to 17.0% are reported in local endogamous subpopulations. We have no idea whether β-thal carrier frequencies or β-thal major (β-TM) births are increasing or decreasing in the population. The cross-sectional nature of all carrier screening programs including large-scale task force and micro level, lack of registration of β-TM births and mechanism to modulate knowledge, awareness programs in a long-term perspective, all preempt impact assessment of preventive programs. During the implementation of a Telangana State Government-sponsored program on 'Micro profiling of β-thalassemia mutations in Telangana,' we documented extensive in-depth demographic information on each β-TM child of the study sample that included age-sex distributions, parental and grand-parental ethnic affiliations (local endogamous group level), birth places, marital migrations, endogamy and consanguinity to identify high-risk districts as ethno-geographic regions. In Telangana State, we found β-thal is widely prevalent in 31 districts and 48 local endogamous subpopulations. The present study provided a method of identification of four 'high-risk districts' and developed a district model for prevention on high priority in Telangana State. The model has the advantage of impact-assessment of all preventive programs in the district.
β-地中海贫血(β-thal)在印度的负担在很大程度上被低估了,一般的携带率为 3.0-4.0%,而在当地的内婚亚群中,报告的携带率高达 17.0%。我们不知道β-地中海贫血携带者频率或β-地中海贫血主要(β-TM)出生在人群中是增加还是减少。所有携带者筛查计划的横断面性质,包括大规模工作队和微观层面,缺乏β-TM 出生的登记和从长远角度调整知识、意识计划的机制,都预先阻止了预防计划的效果评估。在实施一项由泰伦加纳邦政府资助的“泰伦加纳邦β-地中海贫血突变的微观分析”计划期间,我们详细记录了研究样本中每个β-TM 儿童的深入人口统计学信息,包括年龄-性别分布、父母和祖父母的种族归属(当地内婚亚群水平)、出生地、婚姻迁移、内婚和血缘关系,以确定高风险地区作为种族-地理区域。在泰伦加纳邦,我们发现β-地中海贫血在 31 个区和 48 个当地内婚亚群中广泛流行。本研究提供了一种识别四个“高风险区”的方法,并为泰伦加纳邦制定了一个高优先级的预防区模式。该模型具有在该地区评估所有预防计划效果的优势。