Public knowledge, attitudes, and ethical views on CRISPR-Cas9 gene editing for genetic diseases in Taif, Saudi Arabia.

IF 1.8 Q4 GENETICS & HEREDITY
Ghaliah O Alnefaie, Osama H Alsayed, Yusra I Alsalmi, Dhay S Algethami, Mohammed K Alshehri, Maryam S Aljaid
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引用次数: 0

Abstract

Public support for gene editing, particularly for therapeutic purposes, remains strong. Recently, the Ministry of Health in Saudi Arabia approved CRISPR-Cas9 for treating Sickle Cell Disease and beta thalassemia. This study aims to assess the Taif population's opinion on gene editing and their knowledge of genetic modification. In this cross-sectional study, a questionnaire was distributed online from March 2, 2024, to June 15, 2024, to 747 residents of Taif City aged 18 and older. Among the respondents, 14.7% reported that they or their family members suffer from a hereditary disease, and 65.7% either work or study in the healthcare field or have a family member involved in healthcare. Additionally, 50.7% had previously heard of genetic modification. Marital status, number of children, and education level did not significantly influence opinions on genetic editing, whereas affiliation with the healthcare field was significantly associated with greater acceptance (p = 0.023), while a family history of hereditary disease showed a trend toward significance (p = 0.055). Public opinion strongly supports using genetic editing to treat life-threatening diseases in adults and embryos (63.2% and 73.6%, respectively). However, opinions are more divided on non-disease traits. Many respondents expressed interest in enhancing intelligence (73.8%) and strength (75.8%), as well as altering height (67.8%) and hair color (60.7%). While support was strong for therapeutic use, opinions were divided on enhancement, reflecting ethical tension despite high interest in modifying non-disease traits. Notably, 50.7% believed that using genetic editing for non-medical purposes crosses ethical boundaries and exceeds nature's limits. Awareness of gene-editing techniques was not significantly associated with acceptance (p = 0.108). In conclusion, public acceptance of gene editing in Taif is high, particularly among healthcare-affiliated individuals. Increasing public awareness remains essential to bridge ethical concerns and support informed engagement.

沙特阿拉伯塔伊夫关于CRISPR-Cas9基因编辑治疗遗传病的公众知识、态度和伦理观点。
公众对基因编辑,特别是用于治疗目的的基因编辑的支持仍然很强。最近,沙特阿拉伯卫生部批准CRISPR-Cas9用于治疗镰状细胞病和β地中海贫血。本研究旨在评估塔伊夫人群对基因编辑的看法及其对基因改造的了解。本横断面研究于2024年3月2日至2024年6月15日在网上向台伊夫市18岁及以上的747名居民发放调查问卷。在受访者中,14.7%的人报告他们或其家庭成员患有遗传性疾病,65.7%的人在医疗保健领域工作或学习,或有家庭成员从事医疗保健工作。此外,50.7%的人以前听说过基因改造。婚姻状况、子女数量和教育水平对基因编辑的看法没有显著影响,而医疗保健领域的隶属关系与更大的接受度显著相关(p = 0.023),而遗传性疾病的家族史显示出显著的趋势(p = 0.055)。公众舆论强烈支持使用基因编辑来治疗成人和胚胎中的危及生命的疾病(分别为63.2%和73.6%)。然而,对非疾病特征的看法分歧更大。许多受访者表示有兴趣提高智力(73.8%)和力量(75.8%),以及改变身高(67.8%)和头发颜色(60.7%)。虽然对治疗用途的支持很强烈,但对增强的意见分歧,反映了尽管对修改非疾病特征有很高的兴趣,但伦理上的紧张。值得注意的是,50.7%的人认为,将基因编辑用于非医疗目的跨越了伦理界限,超出了自然极限。对基因编辑技术的认知与接受度无显著相关(p = 0.108)。总之,泰国公众对基因编辑的接受程度很高,尤其是在医疗保健相关的个人中。提高公众意识对于消除道德关切和支持知情参与仍然至关重要。
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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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