以色列遗传性视神经萎缩症患者的计划生育,病例系列及伦理考虑因素讨论。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Journal of Neuro-Ophthalmology Pub Date : 2025-06-01 Epub Date: 2024-07-31 DOI:10.1097/WNO.0000000000002232
Eliane Rozanes, Assaf Ben-Arzi, Hagai Boas, Miriam Ehrenberg, Omer Bialer, Hadas Stiebel-Kalish
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引用次数: 0

摘要

背景:遗传性视神经萎缩症患者必须带着视力障碍度过人生的各个阶段,包括计划生育这一重要的里程碑。现在,基因检测技术的进步使医生和受影响的家庭能够考虑通过孕前、植入前和围产期方法提供医疗帮助,以达到预防失明的目的:本病例系列介绍了 4 名患有不同遗传性视神经萎缩症(勒贝尔遗传性视神经病变 [LHON]、常染色体显性遗传性视神经萎缩症、沃尔夫拉姆综合征和乳头状瘤综合征)的患者,他们在 2010 年至 2023 年期间接受了一家三级医疗中心神经眼科部的随访,并处于生育年龄。这项研究旨在加深人们对视神经萎缩症患者计划生育选择的了解,提高人们对现有解决方案的认识,并为临床医生为患者提供支持提供指导:医学、遗传学和医疗技术的进步使得多学科团队能够帮助患者实现生育基因健康后代的愿望。针对每种遗传性视神经萎缩所带来的特殊挑战,可以设计出定制的解决方案。本系列中提出的解决方案是基于对父母进行的基因检测,然后根据检测结果制定个性化的医疗和基因干预计划。本系列文章中选择的解决方案包括在植入前基因诊断(PGD)之前决定不再生育:我们介绍了遗传学的进步如何使 4 种最常见的遗传性视神经萎缩症患者实现了生育无视觉威胁基因突变子女的愿望。我们还回顾了有关 OA 基因突变携带者视神经萎缩渗透性的最新文献,并提出了两个重要的伦理问题:将未来的生命减至无生命威胁的损伤,以及将公共开支用于无生命威胁的疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Family Planning in Genetic Optic Atrophies in Israel, a Case Series and a Discussion of Ethical Considerations.

Background: Patients with genetic optic atrophies must navigate all stages of life with their visual impairment, including the important milestone of family planning. Advances in genetic testing now allows physicians and affected families to consider medical help with the aim of preventing blindness through preconception, preimplantation, and perinatal methods.

Methods: This case series presents 4 patients with different genetic optic atrophies (Leber hereditary optic neuropathy [LHON], autosomal dominant optic atrophy, Wolfram syndrome, and papillorenal syndrome) who were followed by the Neuro-Ophthalmology Unit at a tertiary medical center between 2010 and 2023 and were of child-bearing age. The aim of this study was to increase understanding in family planning options for patients with optic atrophies, raise awareness of the solutions available, and provide guidance for clinicians to support their patients.

Results: Advances in medicine, genetics, and medical technology allow multidisciplinary teams to assist patients in fulfilling their desire for a genetically healthy offspring. Customized solutions can be designed to meet the specific challenges posed by each type of genetic optic atrophy. The solutions proposed in this series are based on genetic testing done in the parents, which then allows to plan medical and genetic intervention individually. The solutions opted for in this series range from the decision to not have another child until PGD (Preimplantation genetic diagnosis).

Conclusions: We describe how genetic advancements have made it possible for patients with the 4 most common hereditary optic atrophies to fulfill their wish to have children without visually threatening genetic mutations. We also review the recent literature on the penetrance of optic atrophy in OA-mutation carriers and raise 2 significant ethical considerations: the reduction of a future life to a non-life-threatening impairment and that of public expenditure for non-life-threatening conditions.

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来源期刊
Journal of Neuro-Ophthalmology
Journal of Neuro-Ophthalmology 医学-临床神经学
CiteScore
2.80
自引率
13.80%
发文量
593
审稿时长
6-12 weeks
期刊介绍: The Journal of Neuro-Ophthalmology (JNO) is the official journal of the North American Neuro-Ophthalmology Society (NANOS). It is a quarterly, peer-reviewed journal that publishes original and commissioned articles related to neuro-ophthalmology.
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