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临床蛋白质组学中的伦理原则、机遇与限制

Ethical principles, opportunities and constraints in clinical proteomics.

作者信息

Porsdam Mann Sebastian, Treit Peter V, Geyer Philipp Emanuel, Omenn Gilbert S, Mann Matthias

机构信息

Uehiro Center for Practical Ethics, University of Oxford, Oxford, UK, Germany.

Max-Planck Institute of Biochemistry, Germany.

出版信息

Mol Cell Proteomics. 2021 Jan 4. doi: 10.1074/mcp.RA120.002435.

DOI:10.1074/mcp.RA120.002435
PMID:33397710
Abstract

Recent advances in MS-based proteomics have vastly increased the quality and scope of biological information that can be derived from human samples. These advances have rendered current workflows increasingly applicable in biomedical and clinical contexts. As proteomics is poised to take an important role in the clinic, associated ethical responsibilities increase in tandem with the impact on the health, privacy, and well-being of individuals. Here we conducted and report a systematic literature review of ethical issues in clinical proteomics. We add our perspectives from a background of bioethics, the results of our accompanying paper extracting individual-sensitive results from patient samples, and the literature addressing similar issues in genomics. The spectrum of potential issues ranges from patient re-identification to incidental findings of clinical significance. The latter can be divided into actionable and unactionable findings. Some of these have the potential to be employed in discriminatory or privacy-infringing ways. However, incidental findings may also have great positive potential. A plasma proteome profile, for instance, could inform on the general health or disease status of an individual regardless of the narrow diagnostic question that prompted it. We suggest that early discussion of ethical issues in clinical proteomics is important to ensure that eventual regulations reflect the considered judgment of the community as well as to anticipate opportunities and problems that may arise as the technology matures further.

摘要

基于质谱的蛋白质组学的最新进展极大地提高了可从人体样本中获取的生物信息的质量和范围。这些进展使当前的工作流程在生物医学和临床环境中越来越适用。随着蛋白质组学有望在临床中发挥重要作用,相关的伦理责任也随着对个人健康、隐私和福祉的影响而同步增加。在此,我们对临床蛋白质组学中的伦理问题进行并报告了一项系统的文献综述。我们从生物伦理学背景出发,阐述了我们的观点,介绍了我们随附论文中从患者样本中提取个体敏感结果的研究结果,以及涉及基因组学中类似问题的文献。潜在问题的范围从患者重新识别到具有临床意义的偶然发现。后者可分为可采取行动的发现和不可采取行动的发现。其中一些发现有可能被用于歧视性或侵犯隐私的方式。然而,偶然发现也可能具有巨大的积极潜力。例如,血浆蛋白质组图谱可以反映一个人的总体健康状况或疾病状态,而不管引发该图谱的具体诊断问题有多狭窄。我们建议,尽早讨论临床蛋白质组学中的伦理问题很重要,这既能确保最终的法规反映社会的审慎判断,又能预见随着技术进一步成熟可能出现的机遇和问题。

相似文献

1
Ethical principles, opportunities and constraints in clinical proteomics.临床蛋白质组学中的伦理原则、机遇与限制
Mol Cell Proteomics. 2021 Jan 4. doi: 10.1074/mcp.RA120.002435.

引用本文的文献

1
Foresight in clinical proteomics: current status, ethical considerations, and future perspectives.临床蛋白质组学的前瞻性:现状、伦理考量及未来展望。
Open Res Eur. 2023 Nov 1;3:59. doi: 10.12688/openreseurope.15810.1. eCollection 2023.