Genetic self-counselors in Tunisia: the role of health education in hemoglobinopathies prevention among high school students.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Foued Maaoui, Imen Moumni, France Arboix-Calas, Ines Safra, Samia Mnif
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Abstract

Background: In Tunisia, the primary prevention of hemoglobinopathies relies on behavioral changes related to screening and genetic counseling. The progression in cognitive and functional literacy in human genetics serves as a crucial aspect of this transformation. In this study, we consider the possibility of genetic self-counseling, checking it in students with scientific or literary backgrounds.

Methods: To assess potential for genetic self-counseling applied to sickle cell disease (SCD), we designed a questionnaire on SCD knowledge (SCDKA), then recruited 356 students (200 scientific students vs. 165 literary students). Since and there were no previous standards for classifying students according to their SCDKA score, we considered participants with an SCDKA score ≥ 70% correct answers as having a high literacy level. Statistical analysis of the results was carried out using chi-square tests and Fisher's, to compare the demographic and educational characteristics of the participants.

Results: The analysis of responses to the various SCDKA items shows a lack of awareness about the hereditary origin of hemoglobinopathies. 97.8% of respondents did not recognize electrophoresis as a diagnostic technique. In terms of genetic literacy, the autosomal and recessive nature of hemoglobinopathies is not well understood. This explains why 41% and 74% of these students could not answer items on genetic transmission. The perception of controllability of hereditary diseases is higher among science students, as is the intention to inform their partner before procreation (56.5% vs. 24.35%, p < 0.001). Responses reveal that science section respondents have higher proactive preventive intentions compared to literature section students, as they recognize the usefulness of genetic counseling (75.5% vs. 47.43%, p < 0.001), premarital diagnosis (57.5% vs. 18.59%, p < 0.001), and prenatal diagnosis (61.5% vs. 13.46%, p < 0.001).

Conclusion: Currently, levels of health literacy and functional genetic literacy do not ensure genetic self-counseling for hemoglobinopathies prevention. The survey shows that having a scientific background was an advantage, but a detailed analysis of these students' results reveals average to low SCDKA scores.

突尼斯的遗传自我咨询师:健康教育在高中生血红蛋白病预防中的作用。
背景:在突尼斯,血红蛋白病的初级预防依赖于与筛查和遗传咨询相关的行为改变。人类遗传学的认知和功能素养的进步是这种转变的关键方面。在这项研究中,我们考虑了基因自我咨询的可能性,在具有科学或文学背景的学生中进行了检查。方法:为了评估基因自我咨询在镰状细胞病(SCD)中的应用潜力,我们设计了一份SCD知识问卷(SCDKA),然后招募了356名学生(200名理科生对165名文科生)。由于以前没有根据SCDKA分数对学生进行分类的标准,因此我们认为SCDKA分数≥70%正确答案的参与者具有较高的识字水平。使用卡方检验和Fisher检验对结果进行统计分析,比较参与者的人口统计学和教育特征。结果:对各种SCDKA项目的反应分析表明缺乏对血红蛋白病遗传起源的认识。97.8%的应答者不承认电泳是一种诊断技术。在遗传知识方面,常染色体和隐性血红蛋白病的性质是不太清楚。这就解释了为什么41%和74%的学生答不出基因传递的问题。理科生对遗传病可控性的认知更高,生育前告知伴侣的意愿也更高(56.5% vs. 24.35%)。结论:目前,健康素养和功能遗传素养水平并不能保证对血红蛋白病预防的遗传自我咨询。调查显示,拥有科学背景是一个优势,但对这些学生结果的详细分析显示,他们的SCDKA分数一般到较低。
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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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