Chapitre 5. From individuals to social: The needs for a global ethics overview in pharmacogenomics.

Anastasia Constantin, Alfonsina Faya Robles, Emmanuelle Rial-Sebbag
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Abstract

As a part of personalized medicine, pharmacogenomics (PGx) allows practitioners to provide the right drug for a given patient, in accordance with the result of a genetic test. This practice raises many ethical issues that are discussed in the literature, sometimes within the larger context of personalized medicine. This article is based on a literature review that is original insofar as it is interdisciplinary and based on an approach that articulates individual and social rights. Here, we propose to reconsider some classic ethical issues, such as informed consent, incidental findings and data protection which are raised by genetic testing and also by PGx in the same or in a different way. We also analyse broader collective issues around racialization and health equality. Our purpose is to contribute in drawing links and parallels between individual rights and collective rights using a social approach. This analysis discusses these ethical issues in research and in clinical setting, understanding the treatment of the individual in his dual quality of patient and research participant.

第 5 章.从个人到社会:药物基因组学全球伦理概览的需求。
作为个性化医疗的一部分,药物基因组学(PGx)允许医生根据基因检测结果为特定患者提供合适的药物。这种做法引发了许多伦理问题,文献中对此进行了讨论,有时是在个性化医疗的大背景下进行讨论。本文以文献综述为基础,具有独创性,因为它是跨学科的,并以阐明个人和社会权利的方法为基础。在此,我们建议重新考虑一些经典的伦理问题,如知情同意、偶然发现和数据保护,这些问题由基因检测和 PGx 以相同或不同的方式提出。我们还分析了围绕种族化和健康平等的更广泛的集体问题。我们的目的是采用社会方法,在个人权利和集体权利之间建立联系和平行关系。本分析讨论了研究和临床环境中的这些伦理问题,理解了个人作为病人和研究参与者的双重身份所受到的待遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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