社会疾病个性化:基于种族的基因组学和个性化医疗分析》。

IF 0.6 Q2 LAW Journal of Law and Medicine Pub Date : 2023-12-01
Josephine Y Lee
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引用次数: 0

摘要

新千年伊始,人类基因组的绘制和测序标志着对基因组科学进行了一次关键性的重新评估,因为它有可能以个性化的方法取代传统的 "一刀切 "医学。在开发药物基因组学产品时使用种族代用品,有可能在减轻健康差异的幌子下将遗传学与种族混为一谈。本文认为,目前实现个性化医疗的基因组学方法并没有兑现为所有人优化健康的承诺,可能会对少数种族群体造成不可逆转的伤害,包括心理、社会和医疗伤害。根据最近的表观遗传学研究结果,文章对基因组和种族进行了重新认识,这对于理解持久的种族差异和种族歧视的累积效应是必要的。然后,文章论述了对批准基于种族的药物基因组学产品进行监管的必要性。
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Personalising Social Ills: An Analysis of Race-based Genomics and Personalised Medicine.

The mapping and sequencing of the human genome at the turn of the new millennium marks a pivotal reassessment of genomic science in its potential to replace traditional "one-size-fits-all" medicine with a personalised approach. The use of racial proxies in the development of pharmacogenomic products risks conflating genetics with race under the guise of alleviating health disparities. This article argues that the current genomic approaches to realising personalised medicine do not deliver on the promise for optimised health for all and may result in irreversible harm, including psychological, social and medical harm, to racial minority groups. In light of recent epigenetic findings, the article provides a reconceptualisation of the genome and race, which is necessary to understand enduring racial disparities and the cumulative effects of racial discrimination. It then addresses the need for regulatory oversight of the approval of race-based pharmacogenomic products.

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CiteScore
0.70
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发文量
63
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