Urgent call for compulsory premarital screening: a crucial step towards thalassemia prevention in Bangladesh.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-09-06 DOI:10.1186/s13023-024-03344-1
Md Jubayer Hossain, Manisha Das, Ummi Rukaiya Munni
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Abstract

Thalassemia poses a major public health concern in Bangladesh with a high prevalence of carriers. However, there is a substantial knowledge gap regarding its epidemiology, clinical aspects, and treatment outcomes. Despite its high prevalence, there is a notable lack of awareness regarding thalassemia in the Bangladeshi population. The absence of precisely validated data impedes a comprehensive understanding of this disease.Premarital thalassemia screening is reportedly a successful strategy for countries such as Saudi Arabia and Iran and has also been proposed for Bangladesh. Mandatory screening coupled with genetic counseling is promising for reducing the prevalence of thalassemia by identifying carriers and providing relevant health education. However, sociocultural barriers, challenges, financial constraints, and health risks associated with prenatal diagnosis and abortion could hinder the success of such programs.Positive outcomes from other countries underscore the effectiveness of such programs in reducing thalassemia incidence. The early identification of carriers and genetic counseling can significantly reduce the burden of thalassemia. Additionally, the strain on the healthcare system would be eased, and the quality of life of thalassemia patients would be improved.In conclusion, based on evidence mandatory premarital screening with genetic counseling could be an effective measure to reduce the prevalence of thalassemia in Bangladesh. Leveraging positive attitudes, adopting successful international models, and addressing existing challenges are crucial for the successful implementation of programs that contribute to the overall health and well-being of the country's population.

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紧急呼吁进行强制性婚前筛查:孟加拉国预防地中海贫血症的关键一步。
地中海贫血症是孟加拉国的一个重大公共卫生问题,其携带者发病率很高。然而,关于地中海贫血症的流行病学、临床方面和治疗效果的知识还存在很大差距。尽管地中海贫血症发病率很高,但孟加拉国民众对地中海贫血症的认识明显不足。据报道,在沙特阿拉伯和伊朗等国,婚前地中海贫血筛查是一项成功的策略,也有人建议在孟加拉国进行筛查。强制筛查与遗传咨询相结合,通过识别携带者和提供相关的健康教育,有望降低地中海贫血症的患病率。然而,与产前诊断和人工流产相关的社会文化障碍、挑战、经济限制和健康风险可能会阻碍此类计划的成功。其他国家的积极成果强调了此类计划在降低地中海贫血发病率方面的有效性。及早发现携带者并提供遗传咨询可大大减轻地中海贫血的负担。此外,医疗系统的压力也将得到缓解,地中海贫血患者的生活质量也将得到改善。总之,根据证据,强制婚前筛查和遗传咨询可能是降低孟加拉国地中海贫血发病率的有效措施。利用积极的态度、采用成功的国际模式以及应对现有的挑战,对于成功实施有助于该国人口整体健康和福祉的计划至关重要。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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