Morley Katherine I, Hall Wayne D
Office of Public Policy and Ethics, Institute for Molecular Bioscience, University of Queensland, 4072 St. Lucia, Queensland, Australia.
J Mol Med (Berl). 2004 Jan;82(1):21-30. doi: 10.1007/s00109-003-0496-x. Epub 2003 Nov 4.
Current pharmacotherapies for psychiatric disorders are generally incompletely effective. Many patients do not respond well or suffer adverse reactions to these drugs, which can result in poor patient compliance and poor treatment outcome. Adverse drug reactions and non-response are likely to be influenced by genetic polymorphisms. Pharmacogenetics holds some promise for improving the treatment of mood disorders by utilising information about genetic polymorphisms to match patients to the drug therapy that is the most effective with the fewest side effects. Pharmacogenomics promises to facilitate the development of new drugs for treatment. However, these technologies raise many ethical, economic and regulatory issues that need to be addressed before they can be integrated into psychiatry, and medicine more generally. We discuss ethical and policy issues arising from pharmacogenetic testing and pharmacogenomics research, such as informed consent, privacy and confidentiality, research on vulnerable persons and discrimination; and economic viability of pharmacogenetics and pharmacogenomics. We conclude with recommendations for the regulation and distribution of pharmacogenetic testing services and pharmacogenomic drugs.
目前用于治疗精神疾病的药物疗法总体上效果并不完全理想。许多患者对这些药物反应不佳或出现不良反应,这可能导致患者依从性差和治疗效果不佳。药物不良反应和无反应可能受基因多态性影响。药物遗传学有望通过利用基因多态性信息,为患者匹配副作用最少且最有效的药物疗法,从而改善情绪障碍的治疗。药物基因组学有望促进新型治疗药物的研发。然而,在这些技术能够更广泛地融入精神病学及医学之前,会引发许多伦理、经济和监管问题,需要加以解决。我们讨论了药物遗传学检测和药物基因组学研究引发的伦理和政策问题,如知情同意、隐私和保密、对弱势群体的研究以及歧视;还讨论了药物遗传学和药物基因组学的经济可行性。最后,我们对药物遗传学检测服务和药物基因组学药物的监管与分发提出了建议。