Ostrer H, Allen W, Crandall L A, Moseley R E, Dewar M A, Nye D, McCrary S V
Department of Pediatrics, New York University Medical Center, New York 10016.
Am J Hum Genet. 1993 Mar;52(3):565-77.
Basic research will spur development of genetic tests that are capable of presymptomatic prediction of disease, disability, and premature death in presently asymptomatic individuals. Concerns have been expressed about potential harms related to the use of genetic test results, especially loss of confidentiality, eugenics, and discrimination. Existing laws and administrative policies may not be sufficient to assure that genetic information is used fairly. To provide factual information and conceptual principles upon which sound social policy can be based, the Human Genome Initiative established an Ethical, Legal, and Social Issues Program. Among the first areas to be identified as a priority for study was insurance. This paper provides a review of life, health, and disability insurance systems, including basic principles, risk classification, and market and regulatory issues, and examines the potential impact of genetic information on the insurance industry.
基础研究将推动基因检测的发展,这种检测能够在目前无症状的个体中对疾病、残疾和过早死亡进行症状前预测。人们对基因检测结果的使用所带来的潜在危害表示担忧,尤其是保密性的丧失、优生学和歧视问题。现有的法律和行政政策可能不足以确保基因信息得到公平使用。为了提供可靠的社会政策可以依据的事实信息和概念原则,人类基因组计划设立了一个伦理、法律和社会问题项目。保险是首批被确定为优先研究领域之一。本文回顾了人寿、健康和残疾保险系统,包括基本原则、风险分类以及市场和监管问题,并探讨了基因信息对保险业的潜在影响。