Consanguinity in the Lebanese population: knowledge, attitudes and practices.

IF 1.8 Q4 GENETICS & HEREDITY
Eliane Chouery, José-Noel Ibrahim, Mary E Deeb, Ali Sobh, Mohamad Ghanem, Jeanine Sobh, Francesca El Choueiry, Ramy Rashwan, Dana Swaidan, Aya Abdelrazzak, Christian Massad, Adam El Fouani, Cybel Mehawej, Andre Megarbane
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Abstract

Consanguinity is associated with an increased risk of autosomal recessive diseases. Its prevalence varies globally, with notably high prevalence in Middle-Eastern countries. Gaining insight into both the prevalence of consanguineous marriages and societal attitudes toward them is essential for designing effective public health interventions. This study examines the current prevalence of consanguinity in Lebanon and explores its contributing risk factors. It further evaluates the knowledge of the Lebanese population regarding this practice and premarital genetic screening, as well as their attitudes toward consanguinity and genetic counseling. A cross-sectional survey was conducted among 984 Lebanese individuals, aged 18 to 65 years, using an online self-administered questionnaire. The prevalence of consanguinity in Lebanon was found to be 24.5%, with first-cousin marriages comprising 46.5% of these unions; place of residence was the only independent factors affecting consanguinity prevalence among our sample. Most participants had a good understanding of consanguinity but misconceptions about specific genetic risks persisted. Attitudes varied, with participants from consanguineous backgrounds showing greater acceptance of the practice. Logistic regression identified gender, education, occupational status, and age as independent predictors of consanguinity while insufficient income, having consanguineous parents, and having a poor knowledge were associated with a positive attitude towards consanguinity. While the prevalence of consanguinity remains high and consistent over time, societal beliefs and cultural practices continue to influence this phenomenon. Public health interventions should focus on raising awareness and disseminating accurate information about the implications of consanguinity and the importance of genetic counseling, particularly among communities with high prevalence of consanguinity.

黎巴嫩人口中的血缘关系:知识、态度和做法。
亲属关系与常染色体隐性遗传病的风险增加有关。其流行率在全球各不相同,中东国家的流行率尤其高。深入了解近亲婚姻的普遍程度和社会对近亲婚姻的态度,对于设计有效的公共卫生干预措施至关重要。本研究考察了目前在黎巴嫩流行的血缘关系,并探讨了其贡献的危险因素。它进一步评估黎巴嫩人口对这种做法和婚前遗传筛查的知识,以及他们对血缘关系和遗传咨询的态度。采用在线自我管理问卷,对984名年龄在18至65岁之间的黎巴嫩人进行了横断面调查。在黎巴嫩,血缘关系的患病率为24.5%,其中表兄弟婚姻占46.5%;居住地是影响我们样本中亲属患病率的唯一独立因素。大多数参与者对血缘关系有很好的理解,但对特定遗传风险的误解仍然存在。人们的态度各不相同,来自血缘背景的参与者对这种做法的接受程度更高。Logistic回归发现,性别、教育程度、职业状况和年龄是亲属关系的独立预测因子,而收入不足、有近亲父母和知识贫乏与对亲属关系的积极态度相关。虽然随着时间的推移,血缘关系的普遍程度仍然很高,而且始终如一,但社会信仰和文化习俗继续影响着这一现象。公共卫生干预措施应侧重于提高认识和传播有关近亲关系影响和遗传咨询重要性的准确信息,特别是在近亲关系高发的社区。
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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