从大脑数据中了解心理:预测的挑战和依赖客观心理数据的公平性。

IF 2.3 3区 哲学 Q1 ETHICS
Jennifer A. Chandler
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引用次数: 0

摘要

本文是研究从大脑数据推断精神状态的伦理和社会影响的系列文章中的第二篇。它考虑了两个主要主题。首先,它讨论了从当前的大脑活动延伸到精神状态,并从那里延伸到未来的精神状态或行为的推理的挑战。当多个推理模型依次应用时,存在复合错误的风险;对统计模型中代表性不足的少数群体可能造成有害的后果。此外,基于大脑数据的预测可能会产生自我实现的预言,强化削弱个人能动性的神经本质主义信念。其次,本文讨论了当从大脑数据推断出精神状态时,与认知不公正相关的担忧是如何产生的。特别是,它提出的问题是,是否只是将“客观的”基于大脑的结论置于个人的主观自我报告之上。虽然基于大脑的证据可以让一些人证明自己的观点,但它也可能加剧可信度差距和社会偏见。这篇文章的结论是,在做出具有社会意义的决定之前,仔细的、具体情况的评估是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Knowing the Mind from Brain Data: The Challenge of Prediction and the Fairness of Relying on Objective Data about the Mind

This article is the second in a series examining the ethical and social implications of inferring mental states from brain data. It considers two main topics. First, it discusses the challenges of extending inferences from present brain activity to mental states and from there to future mental states or behaviors. There is a risk of compounded errors when multiple inferential models are applied sequentially; harmful outcomes for minority groups underrepresented in statistical models could result. In addition, predictions based on brain data may create self-fulfilling prophecies, reinforcing neuroessentialist beliefs that undermine personal agency. Second, the paper discusses how concerns related to epistemic injustice might arise when mental states are inferred from brain data. In particular, it asks if it is just to privilege “objective” brain-based conclusions over individuals’ subjective self-reports. While brain-based evidence could empower some people to prove their claims, it may also exacerbate credibility gaps and social biases. The article concludes that careful, context-specific assessments are essential before brain-based inferences are adopted in socially significant decisions.

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来源期刊
Hastings Center Report
Hastings Center Report 医学-卫生保健
CiteScore
3.50
自引率
3.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: The Hastings Center Report explores ethical, legal, and social issues in medicine, health care, public health, and the life sciences. Six issues per year offer articles, essays, case studies of bioethical problems, columns on law and policy, caregivers’ stories, peer-reviewed scholarly articles, and book reviews. Authors come from an assortment of professions and academic disciplines and express a range of perspectives and political opinions. The Report’s readership includes physicians, nurses, scholars, administrators, social workers, health lawyers, and others.
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