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印度特伦甘纳邦β-地中海贫血症防治高风险区的识别和建立

Identification and Development of a High-Risk District Model in the Prevention of β-Thalassemia in Telangana State, India.

机构信息

Thalassemia and Sickle Cell Society, Raghavendra Colony, Rajendra Nagar, Rangareddy District, Hyderabad, Telangana State, India.

Genome Foundation, Banjara Hills, Hyderabad, Telangana State, India.

出版信息

Hemoglobin. 2020 Sep;44(5):371-375. doi: 10.1080/03630269.2020.1814805. Epub 2020 Oct 2.

DOI:10.1080/03630269.2020.1814805
PMID:33003974
Abstract

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.

摘要

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。

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