多因素疾病遗传风险预测的伦理、法律和社会影响:一项叙述性综述,确定了对多基因评分的解释和使用的担忧。

IF 1.5 Q4 GENETICS & HEREDITY
Journal of Community Genetics Pub Date : 2023-10-01 Epub Date: 2022-12-19 DOI:10.1007/s12687-022-00625-9
Carolyn Riley Chapman
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引用次数: 2

摘要

基因组学的进步使得多基因评分(PGS),有时被称为多基因风险评分,在癌症、心血管疾病和精神分裂症等多因素疾病和病症的背景下得以发展。PGS估计个体与群体中其他成员相比,在受遗传和环境因素影响的情况下的遗传倾向。人们对在公共卫生、临床护理和研究环境中使用PGS提供的遗传风险预测非常感兴趣,但许多人承认需要深思熟虑地考虑和解决伦理、法律和社会影响(ELSI)。为了促进这项工作,本文对该领域学者提出的文献进行了叙述性综述,目的是识别和分类与多因素疾病背景下的遗传风险预测相关的ELSI。从1977年到2021年的92篇文章符合本研究的纳入标准。已确定的ELSI包括潜在利益、挑战和风险,重点关注解释和使用方面的问题,以及最大限度地提高利益、最大限度地减少风险、促进正义和支持自主性的道德义务。这项研究将支持遗传学家、临床医生、遗传顾问、患者、患者权益倡导者和政策制定者认识和解决与PGS相关的伦理问题;它还将指导未来的实证和规范研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ethical, legal, and social implications of genetic risk prediction for multifactorial disease: a narrative review identifying concerns about interpretation and use of polygenic scores.

Advances in genomics have enabled the development of polygenic scores (PGS), sometimes called polygenic risk scores, in the context of multifactorial diseases and disorders such as cancer, cardiovascular disease, and schizophrenia. PGS estimate an individual's genetic predisposition, as compared to other members of a population, for conditions which are influenced by both genetic and environmental factors. There is significant interest in using genetic risk prediction afforded through PGS in public health, clinical care, and research settings, yet many acknowledge the need to thoughtfully consider and address ethical, legal, and social implications (ELSI). To contribute to this effort, this paper reports on a narrative review of the literature, with the aim of identifying and categorizing ELSI relating to genetic risk prediction in the context of multifactorial disease, which have been raised by scholars in the field. Ninety-two articles, spanning from 1977 to 2021, met the inclusion criteria for this study. Identified ELSI included potential benefits, challenges and risks that focused on concerns about interpretation and use, and ethical obligations to maximize benefits, minimize risks, promote justice, and support autonomy. This research will support geneticists, clinicians, genetic counselors, patients, patient advocates, and policymakers in recognizing and addressing ethical concerns associated with PGS; it will also guide future empirical and normative research.

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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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