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从道德角度论证可遗传基因组编辑需要对遗传学采取一种不适当的决定论观点。

The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics.

机构信息

Department of Clinical Ethics and Law, Faculty of Medicine, University of Southampton, Southampton, UK.

出版信息

J Med Ethics. 2019 Aug;45(8):526-527. doi: 10.1136/medethics-2019-105390. Epub 2019 Mar 12.

DOI:10.1136/medethics-2019-105390
PMID:30862707
Abstract

Gyngell and colleagues consider that the recent Nuffield Council report does not go far enough: heritable genome editing (HGE) is not just justifiable in a few rare cases; instead, there is a moral imperative to undertake it. We agree that there is a moral argument for this, but in the real world it is mitigated by the fact that it is not usually possible to ensure a better life. We suggest that a moral imperative for HGE can currently only be concluded if one first buys into an overly deterministic view of a genome sequence, and the role of variation within in it, in the aetiology of the disease: most diseases cannot simply be attributed to specific genetic variants that we could edit away. Multiple, poorly understood genetic and environmental factors interact to influence the expression of diseases with a genetic component, even well understood 'monogenic' disorders. Population-level genome analyses are now demonstrating that many genetic 'mutations' are much less predictive than previously thought Furthermore, HGE might introduce new risks just as it reduces old ones; or remove protections not yet clearly delineated.

摘要

金格尔和同事们认为,最近的纳菲尔德理事会报告做得还不够:可遗传性基因组编辑(HGE)不仅仅在少数几种罕见情况下是合理的;相反,进行 HGE 是有道德义务的。我们同意这是有道德论据的,但在现实世界中,由于通常不可能确保更好的生活,这种情况有所缓解。我们认为,只有当人们首先接受基因组序列的过度决定论观点,以及其内在变异在疾病发病机制中的作用时,HGE 才具有道德必要性:大多数疾病不能简单地归因于我们可以编辑掉的特定遗传变体。多种未被充分理解的遗传和环境因素相互作用,影响具有遗传成分的疾病的表达,即使是被很好理解的“单基因”疾病也是如此。人群水平的基因组分析现在表明,许多遗传“突变”的预测性远不如以前认为的那么高。此外,HGE 可能会引入新的风险,就像它减少旧的风险一样;或者消除尚未明确划定的保护措施。

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